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Patent Analysis of

Liquid crystal alignment agent, liquid crystal alignment film, and liquid crystal display element

Updated Time 12 June 2019

Patent Registration Data

Publication Number

US10000702

Application Number

US14/932988

Application Date

05 November 2015

Publication Date

19 June 2018

Current Assignee

CHI MEI CORPORATION

Original Assignee (Applicant)

CHI MEI CORPORATION

International Classification

C09K19/56,C08L79/08,C09K19/20,C09K19/36

Cooperative Classification

C09K19/56,C08L79/08,C09K19/20,C09K19/2014,C09K19/36

Inventor

HUANG, WAN-TING

Patent Images

This patent contains figures and images illustrating the invention and its embodiment.

US10000702 Liquid crystal alignment agent, liquid 1 US10000702 Liquid crystal alignment agent, liquid 2 US10000702 Liquid crystal alignment agent, liquid 3
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Abstract

A liquid crystal alignment agent capable of forming a liquid crystal display element having good resistance to ultraviolet decay and no mura effect, a liquid crystal alignment film, and a liquid crystal display element having the same are provided. The liquid crystal alignment agent includes a polymer (A), a polysiloxane (B), a polymerizable compound (C) containing a benzophenone structure, and a solvent (D). The polymer (A) is obtained by reacting a mixture. The mixture includes a tetracarboxylic dianhydride component (a1) and a diamine component (a2). The polysiloxane (B) contains a polymerizable unsaturated group, wherein the polymerizable unsaturated group includes a group represented by formula (1-1), a group represented by formula (1-2), or a combination of the two.

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Claims

1. A liquid crystal alignment agent, comprising: a polymer (A); a polysiloxane (B); a polymerizable compound (C) containing a benzophenone structure; and a solvent (D), wherein the polymer (A) is obtained by reacting a mixture, and the mixture comprises a tetracarboxylic dianhydride component (a1) and a diamine component (a2), the polysiloxane (B) contains a polymerizable unsaturated group, and the polymerizable unsaturated group comprises a group represented by formula (1-1), a group represented by formula (1-2), or a combination of the two, in formula (1-1), A represents a hydrogen atom or a methyl group; a represents an integer of 1 to 3, in formula (1-2), b represents an integer of 0 or 1, the polymerizable compound (C) containing a benzophenone structure has at least one photoreactive group selected from the group consisting of formula (3a) to formula (3d), in formula (3a) to formula (3d), R1 represents a hydrogen atom or a C1 to C4 alkyl group; Z1 represents a divalent aromatic ring group or a divalent heterocyclic group that may be substituted by a C1 to C12 alkyl group or a C1 to C12 alkoxy group; Z2 represents a monovalent aromatic ring group or a monovalent heterocyclic group that may be substituted by a C1 to C12 alkyl group or a C1 to C12 alkoxy group.

2. The liquid crystal alignment agent of claim 1, wherein the polysiloxane (B) further contains a group selected from the group consisting of formula (2-1), a group represented by formula (2-2), and a group represented by formula (2-3), in formula (2-1), B represents an oxygen atom or a single bond; c represents an integer of 1 to 3; d represents an integer of 0 to 6, wherein when d represents 0, B is a single bond, in formula (2-2), e represents an integer of 0 to 6, in formula (2-3), D represents a C2 to C6 alkylene group; E represents a hydrogen atom or a C1 to C6 alkyl group.

3. The liquid crystal alignment agent of claim 1, wherein the benzophenone structure contained in the polymerizable compound (C) containing a benzophenone structure is at least one selected from the group consisting of formula (3-1) to formula (3-7),

4. The liquid crystal alignment agent of claim 1, wherein the polymerizable compound (C) containing a benzophenone structure has two or more photoreactive groups.

5. The liquid crystal alignment agent of claim 1, wherein an imidization ratio of the polymer (A) is 30% to 90%.

6. The liquid crystal alignment agent of claim 1, wherein based on 100 parts by weight of the polymer (A), a usage amount of the polysiloxane (B) is 1 part by weight to 25 parts by weight; a usage amount of the polymerizable compound (C) containing a benzophenone structure is 3 parts by weight to 30 parts by weight; a usage amount of the solvent (D) is 800 parts by weight to 4000 parts by weight.

7. A liquid crystal alignment film formed by the liquid crystal alignment agent of claim 1.

8. A liquid crystal display element, comprising the liquid crystal alignment film of claim 7.

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Claim Tree

  • 1
    1), A represents a hydrogen atom or a methyl group; a represents an integer of 1 to 3, in formula (1-2), b represents an integer of 0 or 1, the polymerizable compound (C) containing
    • a benzophenone structure has at least one photoreactive group selected from the group consisting of formula (3a) to formula (3d), in formula (3a) to formula (3d), R1 represents a hydrogen atom or a C1 to C4 alkyl group
    • Z1 represents a divalent aromatic ring group or a divalent heterocyclic group that may be substituted by a C1 to C12 alkyl group or a C1 to C12 alkoxy group
    • Z2 represents a monovalent aromatic ring group or a monovalent heterocyclic group that may be substituted by a C1 to C12 alkyl group or a C1 to C12 alkoxy group.
    • 2. The liquid crystal alignment agent of claim 1, wherein
      • the polysiloxane (B) further contains a group selected from the group consisting of formula (2-
    • 3. The liquid crystal alignment agent of claim 1, wherein
      • the benzophenone structure contained in the polymerizable compound (C) containing
    • 4. The liquid crystal alignment agent of claim 1, wherein
      • the polymerizable compound (C) containing
    • 5. The liquid crystal alignment agent of claim 1, wherein
      • an imidization ratio of the polymer (A) is 30% to 90%.
    • 6. The liquid crystal alignment agent of claim 1, wherein
      • based on 100 parts by weight of the polymer (A), a usage amount of the polysiloxane (B) is 1 part by weight to 25 parts by weight; a usage amount of the polymerizable compound (C) containing
    • 7. A liquid crystal alignment film formed by the liquid crystal alignment agent of claim 1.
  • 8
    8. A liquid crystal display element, comprising
    • the liquid crystal alignment film of claim 7.
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Description

CROSS-REFERENCE TO RELATED APPLICATION

This application claims the priority benefit of Taiwan application serial no. 103138333, filed on Nov. 5, 2014. The entirety of the above-mentioned patent application is hereby incorporated by reference herein and made a part of this specification.

BACKGROUND OF THE INVENTION

Field of the Invention

The invention relates to a liquid crystal alignment agent, a liquid crystal alignment film, and a liquid crystal display element. More particularly, the invention relates to a liquid crystal alignment agent capable of forming a liquid crystal alignment element having good resistance to ultraviolet decay and no mura defect, a liquid crystal alignment film formed by the liquid crystal alignment agent, and a liquid crystal display element having the liquid crystal alignment film.

Description of Related Art

With the development of the liquid crystal display toward a large-size display specification, in order to overcome the issue of viewing angle of a large-size display, the wide-viewing angle techniques of the liquid crystal display panel also need to continuously progress and advance. The multi-domain vertical alignment (MVA)-type liquid crystal display panel is a common wide-viewing angle technique. In the MVA-type liquid crystal display panel, a protrusion is formed in the liquid crystal panel, and the protrusion can limit the tilting direction of a liquid crystal molecule, thereby achieving the display effect of wide-viewing angle. However, the MVA-type liquid crystal display panel cannot prevent the issues of insufficient transmittance and contrast and slow response speed of the liquid crystal molecule originating from the protrusion.

In recent years, to solve the above issues, a polymer-sustained alignment (PSA)-type technique has currently been developed. In the technique, a liquid crystal composition containing a polymerizable compound is clamped in the gap of a pair of substrates formed by a substrate having a patterned conductive film and a substrate without a patterned conductive film or in the gap of a pair of substrates formed by two substrates each having a patterned conductive film, and ultraviolet is irradiated on the liquid crystal composition when voltage is applied between the conductive films to perform polymerization on the polymerizable compound. As a result, pre-tilt angle characteristics are exhibited, and the direction of liquid crystal alignment is controlled. The technique can make the conductive films form a specific structure to achieve the effects of wide-viewing angle and increased response speed of a liquid crystal molecule, thus solving the inevitable issues of insufficient transmittance and contrast of the MVA-type liquid crystal display panel.

However, to generate polymerization to the polymerizable compound, a large amount of ultraviolet of, for instance, 100,000 J/m2 needs to be irradiated. Therefore, in addition to the concern that liquid crystal molecules may be decomposed, unreacted compounds that are not polymerized from ultraviolet irradiation also remain in the liquid crystal layer to form impurity contamination, such that the issue of mura defect is generated to the liquid crystal display element, which in particular has a negative effect on electrical characteristics. Moreover, the type of the liquid crystal molecule used in the liquid crystal layer also needs to correspond to the added polymerizable compound, and is therefore limited.

Therefore, how to solve the issue of impurity contamination of the liquid crystal layer and provide a liquid crystal display element having good resistance to ultraviolet decay and no mura defect is a currently researched topic of those skilled in the art.

SUMMARY OF THE INVENTION

Accordingly, the invention has researched and developed a surface-controlled vertical alignment (SCVA) technique, and provides a liquid crystal alignment agent capable of forming a liquid crystal display element having good resistance to ultraviolet decay and no mura defect, a liquid crystal alignment film formed by the liquid crystal alignment agent, and a liquid crystal display element having the liquid crystal alignment film.

The invention provides a liquid crystal alignment agent including a polymer (A), a polysiloxane (B), a polymerizable compound (C) containing a benzophenone structure, and a solvent (D). The polymer (A) is obtained by reacting a mixture. The mixture includes a tetracarboxylic dianhydride component (a1) and a diamine component (a2). The polysiloxane (B) contains a polymerizable unsaturated group, wherein the polymerizable unsaturated group includes a group represented by formula (1-1), a group represented by formula (1-2), or a combination of the two.

Specifically, the group represented by formula (1-1) is as shown below.

In formula (1-1), A represents a hydrogen atom or a methyl group; a represents an integer of 1 to 3.

Moreover, the group represented by formula (1-2) is as shown below.

In formula (1-2), b represents an integer of 0 or 1.

In an embodiment of the invention, the polysiloxane (B) further contains a group containing an epoxy group, and the group containing an epoxy group includes at least one of a group represented by formula (2-1), a group represented by formula (2-2), and a group represented by formula (2-3).

Specifically, the group represented by formula (2-1) is as shown below.

In formula (2-1), B represents a hydrogen atom or a single bond; c represents an integer of 1 to 3; d represents an integer of 0 to 6, wherein when d represents 0, and B is a single bond.

Moreover, the group represented by formula (2-2) is as shown below.

In formula (2-2), e represents an integer of 0 to 6.

The group represented by formula (2-3) is as shown below.

In formula (2-3), D represents a C2 to C6 alkylene group; E represents a hydrogen atom or a C1 to C6 alkyl group.

In an embodiment of the invention, the benzophenone structure contained in the polymerizable compound (C) containing a benzophenone structure is at least one selected from the group consisting of formula (3-1) to formula (3-7),

In an embodiment of the invention, the polymerizable compound (C) containing a benzophenone structure has two or more photoreactive groups.

In an embodiment of the invention, the imidization ratio of the polymer (A) is 30% to 90%.

In an embodiment of the invention, based on 100 parts by weight of the polymer (A), the usage amount of the polysiloxane (B) is 1 part by weight to 25 parts by weight; the usage amount of the polymerizable compound (C) containing a benzophenone structure is 3 parts by weight to 30 parts by weight; the usage amount of the solvent (D) is 800 parts by weight to 4000 parts by weight.

The invention further provides a liquid crystal alignment film. The liquid crystal alignment film is formed by the above liquid crystal alignment agent.

The invention further provides a liquid crystal display element. The liquid crystal display element includes the above liquid crystal alignment film.

Based on the above, in the SCVA-type liquid crystal alignment agent of the invention, in addition to containing a polymer and a solvent, a polymerizable compound containing a benzophenone structure is further added in the liquid crystal alignment agent. As a result, the issue of impurity contamination of a liquid crystal layer does not occur. More specifically, the SCVA-type liquid crystal alignment agent of the invention contains both a polysiloxane containing a specific structure and a polymerizable compound containing a benzophenone structure, such that the resistance to ultraviolet decay of the liquid crystal display element is good, and the liquid crystal display element does not have the issue of mura defect. As a result, the liquid crystal alignment agent of the invention is suitable for the fabrication of a liquid crystal alignment film and a liquid crystal display element.

To make the above features and advantages of the invention more comprehensible, several embodiments are described in detail as follows.

DESCRIPTION OF THE EMBODIMENTS

<Liquid Crystal Alignment Agent>

The invention provides a liquid crystal alignment agent including a polymer (A), a polysiloxane (B), a polymerizable compound (C) containing a benzophenone structure, and a solvent (D). Moreover, the liquid crystal alignment agent can further include an additive (E) if needed.

In the following, each component of the liquid crystal alignment agent of the invention is described in detail.

It should be mentioned that, in the following, (meth)acrylic acid represents acrylic acid and/or methacrylic acid, and (meth)acrylate represents acrylate and/or methacrylate. Similarly, (meth)acryloyl group represents acryloyl group and/or methacryloyl group.

Polymer (A)

The polymer (A) is obtained by reacting a mixture. The mixture includes a tetracarboxylic dianhydride component (a1) and a diamine component (a2).

Specifically, the polymer (A) includes a polyamic acid, a polyimide, a polyamic acid-polyimide block copolymer, or a combination of the polymers. In particular, the polyimide-based block copolymer includes a polyamic acid block copolymer, a polyimide block copolymer, a polyamic acid-polyimide block copolymer, or a combination of the polymers. The polyamic acid polymer, the polyimide polymer, and the polyamic acid-polyimide block copolymer can all be obtained by reacting a mixture of the tetracarboxylic dianhydride component (a1) and the diamine component (a2).

Tetracarboxylic Dianhydride Component (a1)

The tetracarboxylic dianhydride component (a1) includes an aliphatic tetracarboxylic dianhydride compound, an alicyclic tetracarboxylic dianhydride compound, an aromatic tetracarboxylic dianhydride compound, at least one of the tetracarboxylic dianhydride compounds represented by formula (I-1) to formula (I-6), or a combination of the compounds.

Specific examples of the aliphatic tetracarboxylic dianhydride compound, the alicyclic tetracarboxylic dianhydride compound, and the aromatic tetracarboxylic dianhydride compound are listed below. However, the invention is not limited to the specific examples.

Specific examples of the aliphatic tetracarboxylic dianhydride compound can include, but are not limited to, ethane tetracarboxylic dianhydride, butane tetracarboxylic dianhydride, or a combination of the compounds.

Specific examples of the alicyclic tetracarboxylic dianhydride compound can include, but are not limited to, 1,2,3,4-cyclobutane tetracarboxylic dianhydride, 1,2-dimethyl-1,2,3,4-cyclobutane tetracarboxylic dianhydride, 1,3-dimethyl-1,2,3,4-cyclobutane tetracarboxylic dianhydride, 1,3-dichloro-1,2,3,4-cyclobutane tetracarboxylic dianhydride, 1,2,3,4-tetramethyl-1,2,3,4-cyclobutane tetracarboxylic dianhydride, 2,3,4-cyclopentane tetracarboxylic dianhydride, 2,4,5-cyclohexane tetracarboxylic dianhydride, 3,3′,4,4′-dicyclohexyl tetracarboxylic dianhydride, cis-3,7-dibutyl-cycloheptyl-1,5-diene-1,2,5,6-tetracarboxylic dianhydride, 2,3,5-tricarboxycyclopentylacetic dianhydride, bicyclo[2.2.2]-oct-7-ene-2,3,5,6-tetracarboxylic dianhydride, or a combination of the compounds.

Specific examples of the aromatic tetracarboxylic dianhydride compound can include, but are not limited to, an aromatic tetracarboxylic dianhydride compound such as 3,4-dicarboxy-1,2,3,4-tetrahydronaphthalene-1-succinic dianhydride, pyromellitic dianhydride, 3,3′,4,4′-benzophenone tetracarboxylic dianhydride, 3′,3,4,4′-biphenylsulfone tetracarboxylic dianhydride, 1,4,5,8-naphthalene tetracarboxylic dianhydride, 2,3,6,7-naphthalene tetracarboxylic dianhydride, 3,3′,4,4′-diphenyl ethane tetracarboxylic dianhydride, 3,3′,4,4′-dimethyl diphenyl silane tetracarboxylic dianhydride, 3,3′,4,4′-tetraphenyl silane tetracarboxylic dianhydride, 1,2,3,4-furan tetracarboxylic dianhydride, 4,4′-bis(3,4-dicarboxy phenoxy)diphenylsulfide dianhydride, 4,4′-bis(3,4-dicarboxy phenoxy)diphenylsulfone dianhydride, 4,4′-bis(3,4-dicarboxy phenoxy)diphenylpropane dianhydride, 3,3′,4,4′-perfluoroisopropylidene diphenyl dicarboxylic dianhydride, 3,3′,4,4′-diphenyl tetracarboxylic dianhydride, bis(phthalic acid)phenylphosphine oxide dianhydride, p-phenylene-bis(triphenylphthalic acid)dianhydride, m-phenylene-bis(triphenylphthalic acid)dianhydride, bis(triphenylphthalic acid)-4,4′-diphenylether dianhydride, bis(triphenylphthalic acid)-4,4′-diphenylmethane dianhydride, ethylene glycol-bis(anhydrotrimellitate), propylene glycol-bis(anhydrotrimellitate), 1,4-butanediol-bis(anhydrotrimellitate), 1,6-hexanediol-bis(anhydrotrimellitate), 1,8-octanediol-bis(anhydrotrimellitate), 2,2-bis(4-hydroxyphenyl)propane-bis(anhydrotrimellitate), 2,3,4,5-tetrahydrofuran tetracarboxylic dianhydride, 3,3a,4,5,9b-hexahydro-5-(tetrahydro-2,5-dioxo-3-furanyl)naphtho[1,2-c]furan-1,3-dione, 1,3,3a,4,5,9b-hexahydro-5-methyl-5-(tetrahydro-2,5-dioxo-3-furanyl)naphtho[1,2-c]furan-1,3-dione, 1,3,3a,4,5,9b-hexahydro-5-ethyl-5-(tetrahydro-2,5-dioxo-3-furanyl)naphtho[1,2-c]furan-1,3-dione, 1,3,3a,4,5,9b-hexahydro-7-methyl-5-(tetrahydro-2,5-dioxo-3-furanyl)naphtho[1,2-c]furan-1,3-dione, 3,3a,4,5,9b-hexahydro-7-ethyl-5-(tetrahydro-2,5-dioxo-3-furanyl)naphtho[1,2-c]furan-1,3-dione, 1,3,3a,4,5,9b-hexahydro-8-methyl-5-(tetrahydro-2,5-dioxo-3-furanyl)naphtho[1,2-c]furan-1,3-dione, 3,3a,4,5,9b-hexahydro-8-ethyl-5-(tetrahydro-2,5-dioxo-3-furanyl)naphtho[1,2-c]furan-1,3-dione, 1,3,3a,4,5,9b-hexahydro-5,8-dimethyl-5-(tetrahydro-2,5-dioxo-3-furanyl)naphtho[1,2-c]furan-1,3-dione, 5-(2,5-dioxotetrahydrofural)-3-methyl-3-cyclohexene-1,2-dicarboxylic dianhydride, or a combination of the compounds.

The tetracarboxylic dianhydride compounds represented by formula (I-1) to formula (I-6) are as shown below.

In formula (I-5), A1 represents a divalent group containing an aromatic ring; r represents an integer of 1 to 2; and A2 and A3 can be the same or different, and can each independently represent a hydrogen atom or an alkyl group. Specific examples of the tetracarboxylic dianhydride compound represented by formula (I-5) include at least one of the compounds represented by formula (I-5-1) to formula (I-5-3).

In formula (I-6), A4 represents a divalent group containing an aromatic ring; and A5 and A6 can be the same or different, and each independently represent a hydrogen atom or an alkyl group. The tetracarboxylic dianhydride compound represented by formula (I-6) is preferably a compound represented by formula (I-6-1).

The tetracarboxylic dianhydride component (a1) can be used alone or in multiple combinations.

Specific examples of the tetracarboxylic dianhydride component (a1) preferably include 1,2,3,4-cyclobutane tetracarboxylic dianhydride, 1,2,3,4-cyclopentane tetracarboxylic dianhydride, 2,3,5-tricarboxycyclopentylacetic acid dianhydride, 1,2,4,5-cyclohexane tetracarboxylic dianhydride, 3,4-dicarboxy-1,2,3,4-tetrahydronaphthalene-1-succinic dianhydride, pyromellitic dianhydride, 3,3′,4,4′-benzophenone tetracarboxylic dianhydride, and 3′,3,4,4′-diphenylsulfone tetracarboxylic dianhydride, or a combination of the compounds.

Based on a total number of moles of 100 moles of the diamine component (a2), the usage amount of the tetracarboxylic dianhydride component (a1) preferably ranges from 20 moles to 200 moles; and the usage amount of the tetracarboxylic dianhydride component (a1) more preferably ranges from 30 moles to 120 moles.

Diamine Component (a2)

The diamine component (a2) includes an aliphatic diamine compound, an alicyclic diamine compound, an aromatic diamine compound, diamine compounds having formula (II-1) to formula (II-30), or a combination thereof.

Specific examples of the aliphatic diamine compound include, but are not limited to, 1,2-diaminoethane, 1,3-diaminopropane, 1,4-diaminobutane, 1,5-diaminopentane, 1,6-diaminohexane, 1,7-diaminoheptane, 1,8-diaminooctane, 1,9-diaminononane, 1,10-diaminodecane, 4,4′-diaminoheptane, 1,3-diamino-2,2-dimethylpropane, 1,6-diamino-2,5-dimethylhexane, 1,7-diamino-2,5-dimethylheptane, 1,7-diamino-4,4-dimethylheptane, 1,7-diamino-3-methylheptane, 1,9-diamino-5-methylnonane, 2,11-diaminododecane, 1,12-diaminooctadecane, 1,2-bis(3-aminopropoxy)ethane, or a combination of the compounds.

Specific examples of the alicyclic diamine compound include, but are not limited to, 4,4′-diaminodicyclohexylmethane, 4,4′-diamino-3,3′-dimethyldicyclohexylamine, 1,3-diaminocyclohexane, 1,4-diaminocyclohexane, isophorone diamine, tetrahydrodicyclopentadiene diamine, tricyclo[6.2.1.02,7]-undecylenedimethyldiamine, 4,4′-methylene bis(cyclohexylamine), or a combination of the compounds.

Specific examples of the aromatic diamine compound include, but are not limited to, 4,4′-diaminodiphenylmethane, 4,4′-diaminodiphenylethane, 4,4′-diaminodiphenylsulfone, 4,4′-diaminobenzoylaniline, 4,4′-diaminodiphenylether, 3,4′-diaminodiphenylether, 1,5-diaminonaphthalene, 5-amino-1-(4′-aminophenyl)-1,3,3-trimethylindene, 6-amino-1-(4′-aminophenyl)-1,3,3-trimethylindene, hexahydro-4,7-methanoindanylenedimethylenediamine, 3,3′-diaminobenzophenone, 3,4′-diaminobenzophenone, 4,4′-diaminobenzophenone, 2,2-bis[4-(4-aminophenoxy)phenyl]propane, 2,2-bis[4-(4-aminophenoxy)phenyl]hexafluoropropane, 2,2-bis(4-aminophenyl)hexafluoropropane, 2,2-bis[4-(4-aminophenoxy)phenyl]sulfone, 1,4-bis(4-aminophenoxy)benzene, 1,3-bis(4-aminophenoxy)benzene, 1,3-bis(3-aminophenoxy)benzene, 9,9-bis(4-aminophenyl)-10-hydroanthracene, 9,10-bis(4-aminophenyl)anthracene, 2,7-diaminofluorene, 9,9-bis(4-aminophenyl)fluorene, 4,4′-methylene-bis(2-chloroaniline), 4,4′-(p-phenyleneisopropylidene)bisaniline, 4,4′-(m-phenyleneisopropylidene)bisaniline, 2,2′-bis[4-(4-amino-2-trifluoromethyl phenoxy)phenyl]hexafluoropropane, 4,4′-bis[(4-amino-2-trifluoromethyl)phenoxy]-octafluorobiphenyl, 5-[4-(4-n-pentylcyclohexyl)cyclohexyl]phenylmethylene-1,3-diaminobenzene, 1,1-bis[4-(4-aminophenoxy)phenyl]-4-(4-ethylphenyl)cyclohexane, or a combination of the compounds.

The diamine compounds having formula (II-1) to formula (II-30) are as shown below.

In formula (II-1), B1 represents

and B2 represents a group having a steroid skeleton, a trifluoromethyl group, a fluorine atom, a C2 to C30 alkyl group, or a monovalent group of a cyclic structure containing a nitrogen atom derived from, for instance, pyridine, pyrimidine, triazine, piperidine, or piperazine.

Specific examples of the compound represented by formula (II-1) include, but are not limited to, 2,4-diaminophenyl ethyl formate, 3,5-diaminophenyl ethyl formate, 2,4-diaminophenyl propyl formate, 3,5-diaminophenyl propyl formate, 1-dodecoxy-2,4-diaminobenzene, 1-hexadecoxy-2,4-diaminobenzene, 1-octadecoxy-2,4-diaminobenzene, at least one of the compounds represented by formula (II-1-1) to formula (II-1-6), or a combination of the compounds.

The compounds represented by formula (II-1-1) to formula (II-1-6) are as shown below.

In formula (II-2), B1 is the same as the B1 in formula (II-1), B3 and B4 each independently represent a divalent aliphatic ring, a divalent aromatic ring, or a divalent heterocyclic group; B5 represents a C3 to C18 alkyl group, a C3 to C18 alkoxy group, a C1 to C5 fluoroalkyl group, a C1 to C5 fluoroalkyloxy group, a cyano group, or a halogen atom.

Specific examples of the compound represented by formula (II-2) include at least one of the compounds represented by formula (II-2-1) to formula (II-2-13). Specifically, the compounds represented by formula (II-2-1) to formula (II-2-13) are as follows.

In formula (II-2-10) to formula (II-2-13), s represents an integer of 3 to 12.

In formula (II-3), B6 each independently represents a hydrogen atom, a C1 to C5 acyl group, a C1 to C5 alkyl group, a C1 to C5 alkoxy group, or a halogen atom, and B6 in each repeating unit can be the same or different; u represents an integer of 1 to 3.

Specific examples of the compound represented by formula (II-3) include: when u is 1: p-diaminobenzene, m-diaminobenzene, o-diaminobenzene, or 2,5-diaminotoluene . . . etc.; when u is 2: 4,4′-diaminobiphenyl, 2,2′-dimethyl-4,4′-diaminobiphenyl, 3,3′-dimethyl-4,4′-diaminobiphenyl, 3,3′-dimethoxy-4,4′-diaminobiphenyl, 2,2′-dichloro-4,4′-diaminobiphenyl, 3,3′-dichloro-4,4′-diaminobiphenyl, 2,2′,5,5′-tetrachloro-4,4′-diaminobiphenyl, 2,2′-dichloro-4,4′-diamino-5,5′-dimethoxybiphenyl, or 4,4′-diamino-2,2′-bis(trifluoromethyl) biphenyl . . . etc.; or when u is 3: 1,4-bis(4′-aminophenyl)benzene . . . etc.

Specific examples of the compound represented by formula (II-3) preferably include p-diaminobenzene, 2,5-diaminotoluene, 4,4′-diaminobiphenyl, 3,3′-dimethoxy-4,4′-diaminobiphenyl, 1,4-bis(4′-aminophenyl)benzene, or a combination of the compounds.

In formula (II-4), v represents an integer of 2 to 12.

In formula (II-5), w represents an integer of 1 to 5. The compound represented by formula (II-5) is preferably 4,4′-diamino-diphenyl sulfide.

In formula (II-6), B7 and B9 each independently represent a divalent organic group, and B7 and B9 can be the same or different; B8 represents a divalent group of a cyclic structure containing a nitrogen atom derived from, for instance, pyridine, pyrimidine, triazine, piperidine, or piperazine.

In formula (II-7), B10, B11, B12, and B13 each independently represent a C1 to C12 hydrocarbon group, and B10, B11, B12, and B13 can be the same or different; X1 each independently represents an integer of 1 to 3; X2 represents an integer of 1 to 20.

In formula (II-8), B14 represents an oxygen atom or a cyclohexylene group; B15 represents a methylene group (—CH2); B16 represents a phenylene group or a cyclohexylene group; B17 represents a hydrogen atom or a heptyl group.

Specific examples of the compound represented by formula (II-8) include a compound represented by formula (II-8-1), a compound represented by formula (II-8-2), or a combination of the compounds.

The compounds represented by formula (II-9) to formula (II-30) are as shown below.

In formula (II-17) to formula (II-25), B18 preferably represents a C1 to C10 alkyl group or a C1 to C10 alkoxy group; and B19 preferably represents a hydrogen atom, a C1 to C10 alkyl group, or a C1 to C10 alkoxy group.

The diamine compound (a2) can be used alone or in multiple combinations.

Specific examples of the diamine compound (a2) preferably include, but are not limited to, 1,2-diaminoethane, 4,4′-diaminodicyclohexylmethane, 4,4′-diaminodiphenylmethane, 4,4′-diaminodiphenylether, 5-[4-(4-n-pentylcyclohexyl)cyclohexyl]phenylmethylene-1,3-diaminobenzene, 1,1-bis[4-(4-aminophenoxy)phenyl]-4-(4-ethylphenyl)cyclohexane, 2,4-diaminophenyl ethyl formate, a compound represented by formula (II-1-1), a compound represented by formula (II-1-2), a compound represented by formula (II-1-5), a compound represented by formula (II-2-1), a compound represented by formula (II-2-11), p-diaminobenzene, m-diaminobenzene, o-diaminobenzene, a compound represented by formula (II-8-1), compounds represented by formula (II-26) to formula (II-30), or a combination of the compounds.

When the polymer (A) in the liquid crystal alignment agent contains at least one of the diamine compounds (a2) represented by formula (II-1) and formula (II-2), the issue of mura defect of the liquid crystal display element can be further alleviated.

When the polymer (A) in the liquid crystal alignment agent contains at least one of the diamine compounds (a2) represented by formula (II-26) to formula (II-30), resistance to ultraviolet decay of the liquid crystal display element can be further increased.

Method of Preparing Polymer (A)

The polymer (A) can include at least one of polyamic acid and polyimide. Moreover, the polymer (A) can further include a polyimide-based block copolymer. The preparation method of each of the various polymers above is further described below.

Method of Preparing Polyamic Acid

The method of preparing the polyamic acid includes first dissolving a mixture in a solvent, wherein the mixture includes the tetracarboxylic dianhydride component (a1) and the diamine component (a2). A polycondensation reaction is then performed at a temperature of 0° C. to 100° C. After reacting for 1 hour to 24 hours, the reaction solution is distilled under reduced pressure with an evaporator to obtain the polyamic acid. Alternatively, the reaction solution is poured into a large amount of a poor solvent to obtain a precipitate. Then, the precipitate is dried with a method of drying under reduced pressure to obtain the polyamic acid.

The solvent used in the polycondensation reaction can be the same or different as the solvent in the liquid crystal alignment agent below, and the solvent used in the polycondensation reaction is not particularly limited, provided the solvent can dissolve the reactants and the products. The solvent preferably includes, but is not limited to (1) an aprotic polar solvent such as N-methyl-2-pyrrolidinone (NMP), N,N-dimethyl acetamide, N,N-dimethyl formamide, dimethyl sulfoxide, γ-butyrolactone, tetramethylurea, or hexamethylphosphor amide; or (2) a phenolic solvent such as m-cresol, xylenol, phenol, or halogenated phenol. Based on a total usage amount of 100 parts by weight of the mixture, the usage amount of the solvent used in the polycondensation reaction is preferably 200 parts by weight to 2000 parts by weight, more preferably 300 parts by weight to 1800 parts by weight.

It should be mentioned that, in the polycondensation reaction, the solvent can be used with a suitable amount of a poor solvent, wherein the poor solvent does not cause precipitation of the polyamic acid. The poor solvent can be used alone or in multiple combinations, and includes, but is not limited to (1) an alcohol such as methanol, ethanol, isopropanol, cyclohexanol, ethylene glycol, propylene glycol, 1,4-butanediol, or triglycol; (2) a ketone such as acetone, methyl ethyl ketone, methyl isobutyl ketone, or cyclohexanone; (3) an ester such as methyl acetate, ethyl acetate, butyl acetate, diethyl oxalate, diethyl malonate, or ethylene glycol monoethyl ether acetate; (4) an ether such as diethyl ether, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol n-propyl ether, ethylene glycol isopropyl ether, ethylene glycol n-butyl ether, ethylene glycol dimethyl ether, or diethylene glycol dimethyl ether; (5) a halogenated hydrocarbon such as dichloromethane, 1,2-dichloroethane, 1,4-dichlorobutane, trichloroethane, chlorobenzene, or o-dichlorobenzene; or (6) a hydrocarbon such as tetrahydrofuran, hexane, heptane, octane, benzene, toluene, or xylene, or any combination of the solvents. Based on a usage amount of 100 parts by weight of the diamine component (a2), the usage amount of the poor solvent is preferably 0 parts by weight to 60 parts by weight, more preferably 0 parts by weight to 50 parts by weight.

Method of Preparing Polyimide

The method of preparing the polyimide includes heating the polyamic acid obtained by the above method of preparing polyamic acid under the existence of a dehydrating agent and a catalyst. During the heating process, the amic acid functional group in the polyamic acid can be converted into an imide functional group through a dehydration ring-closure reaction (i.e., imidization).

The solvent used in the dehydration ring-closure reaction can be the same as the solvent (D) in the liquid crystal alignment agent and is therefore not repeated herein. Based on a usage amount of 100 parts by weight of the polyamic acid, the usage amount of the solvent used in the dehydration ring-closure reaction is preferably 200 parts by weight to 2000 parts by weight, more preferably 300 parts by weight to 1800 parts by weight.

To obtain a preferable degree of imidization of the polyamic acid, the operating temperature of the dehydration ring-closure reaction is preferably 40° C. to 200° C., more preferably 40° C. to 150° C. If the operating temperature of the dehydration ring-closure reaction is less than 40° C., then the imidization reaction is incomplete, and the degree of imidization of the polyamic acid is thereby reduced. However, if the operating temperature of the dehydration ring-closure reaction is higher than 200° C., then the weight-average molecular weight of the obtained polyimide is lower.

The dehydrating agent used in the dehydration ring-closure reaction can be selected from an anhydride compound, and specific examples thereof include, for instance, acetic anhydride, propionic anhydride, or trifluoroacetic anhydride. Based on 1 mole of polyamic acid, the usage amount of the dehydrating agent is 0.01 moles to 20 moles. The catalyst used in the dehydration ring-closure reaction can be selected from (1) a pyridine compound such as pyridine, trimethyl pyridine, or dimethyl pyridine; or (2) a tertiary amine compound such as triethylamine. Based on a usage amount of 1 mole of the dehydrating agent, the usage amount of the catalyst can be 0.5 moles to 10 moles.

The imidization ratio of the polymer (A) can be 30% to 90%, preferably 35% to 88%, and more preferably 40% to 85%. When the imidization ratio of the polymer (A) in the liquid crystal alignment agent is within the above ranges, resistance to ultraviolet decay of the liquid crystal display element can be further increased.

Method of Preparing Polyimide-Based Block Copolymer

The polyimide-based block copolymer is selected from a polyamic acid block copolymer, a polyimide block copolymer, a polyamic acid-polyimide block copolymer, or any combination of the polymers.

The method of preparing the polyimide-based block copolymer preferably includes first dissolving a starting material in a solvent and then performing a polycondensation reaction, wherein the starting material includes at least one type of polyamic acid and/or at least one type of polyimide, and can further include a carboxylic anhydride component and a diamine component.

The carboxylic anhydride component and the diamine component in the starting material can be the same as the tetracarboxylic dianhydride component (a1) and the diamine component (a2) used in the method of preparing the polyamic acid. Moreover, the solvent used in the polycondensation reaction can be the same as the solvent in the liquid crystal alignment agent below and is not repeated herein.

Based on a usage amount of 100 parts by weight of the starting material, the usage amount of the solvent used in the polycondensation reaction is preferably 200 parts by weight to 2000 parts by weight, more preferably 300 parts by weight to 1800 parts by weight. The operating temperature of the polycondensation reaction is preferably 0° C. to 200° C., more preferably 0° C. to 100° C.

The starting material preferably includes, but is not limited to (1) two polyamic acids for which the terminal groups are different and the structures are different; (2) two polyimides for which the terminal groups are different and the structures are different; (3) a polyamic acid and a polyimide for which the terminal groups are different and the structures are different; (4) a polyamic acid, a carboxylic anhydride component, and a diamine component, wherein the structure of at least one of the carboxylic anhydride component and the diamine component is different from the structures of the carboxylic anhydride component and the diamine component used to form the polyamic acid; (5) a polyimide, a carboxylic anhydride component, and a diamine component, wherein the structure of at least one of the carboxylic anhydride component and the diamine component is different from the structures of the carboxylic anhydride component and the diamine component used to form the polyimide; (6) a polyamic acid, a polyimide, a carboxylic anhydride component, and a diamine component, wherein the structure of at least one of the carboxylic anhydride component and the diamine component is different from the structures of the carboxylic anhydride component and the diamine component used to form the polyamic acid or the polyimide; (7) two polyamic acids having different structures, a carboxylic anhydride component, and a diamine component; (8) two polyimides having different structures, a carboxylic anhydride component, and a diamine component; (9) two polyamic acids having anhydride groups as terminal groups and having different structures, and a diamine component; (10) two polyamic acids having amine groups as terminal groups and having different structures, and a carboxylic anhydride component; (11) two polyimides having anhydride groups as terminal groups and having different structures, and a diamine component; or (12) two polyimides having amine groups as terminal groups and having different structures, and a carboxylic anhydride component.

Without affecting the efficacy of the invention, the polyamic acid, the polyimide, and the polyimide-based block copolymer are preferably terminal-modified polymers in which molecular weight regulation is first performed. By using the terminal-modified polymers, the coating performance of the liquid crystal alignment agent can be improved. The method of preparing the terminal-modified polymers can include adding a monofunctional compound at the same time a polycondensation reaction is performed on the polyamic acid.

Specific examples of the monofunctional compound include, but are not limited to, (1) a monoanhydride such as maleic anhydride, phthalic anhydride, itaconic anhydride, n-decyl succinic anhydride, n-dodecyl succinic anhydride, n-tetradecyl succinic anhydride, or n-hexadecyl succinic anhydride; (2) a monoamine compound such as aniline, cyclohexylamine, n-butylamine, n-amylamine, n-hexylamine, n-heptylamine, n-octylamine, n-nonylamine, n-decylamine, n-undecylamine, n-dodecylamine, n-tridecylamine, n-tetradecylamine, n-pentadecylamine, n-hexadecylamine, n-heptadecylamine, n-octadecylamine, or n-eicosylamine; or (3) a monoisocyanate compound such as phenyl isocyanate or naphthyl isocyanate.

In the polymer (A) of the invention, the polystyrene-equivalent weight average molecular weight obtained according to gel permeation chromatography (GPC) is 2,000 to 200,000, preferably 3,000 to 100,000, and more preferably 4,000 to 50,000.

Polysiloxane (B)

The polysiloxane (B) contains a polymerizable unsaturated group, and the polymerizable unsaturated group includes a group represented by formula (1-1), a group represented by formula (1-2), or a combination of the two.

Specifically, the group represented by formula (1-1) and the group represented by formula (1-2) are as shown below.

In formula (1-1), A represents a hydrogen atom or a methyl group; a represents an integer of 1 to 3.

In formula (1-2), b represents an integer of 0 or 1.

Specifically, the polysiloxane (B) can further contain a group containing an epoxy group, and the group containing an epoxy group includes at least one of a group represented by formula (2-1), a group represented by formula (2-2), and a group represented by formula (2-3). When the polysiloxane (B) further contains a group containing an epoxy group, the issue of mura defect of the liquid crystal display element can be further alleviated.

Specifically, the group represented by formula (2-1), the group represented by formula (2-2), and the group represented by formula (2-3) are as shown below.

In formula (2-1), B represents a hydrogen atom or a single bond; c represents an integer of 1 to 3; d represents an integer of 0 to 6, wherein when d represents 0, B is a single bond.

Moreover, the group represented by formula (2-2) is as shown below.

In formula (2-2), e represents an integer of 0 to 6.

The group represented by formula (2-3) is as shown below.

In formula (2-3), D represents a C2 to C6 alkylene group; E represents a hydrogen atom or a C1 to C6 alkyl group.

The polysiloxane (B) can be formed from the self-polycondensation of the silane compound (b1) containing a polymerizable unsaturated group; alternatively, the polysiloxane (B) can be formed from the copolycondensation of the silane compound (b1) containing a polymerizable unsaturated group and the silane compound (b2) containing an epoxy group. In addition, without affecting the efficacy of the invention, the monomer forming the polysiloxane (B) can further include other silicon compounds (b3).

Silane Compound (b1) Containing a Polymerizable Unsaturated Group

The polymerizable unsaturated group contained in the silane compound (b1) containing a polymerizable unsaturated group includes the group represented by formula (1-1), the group represented by formula (1-2), or a combination thereof.

Specific examples of the silane compound (b1) containing a polymerizable unsaturated group include 3-(meth)acryloxypropyl trichlorosilane, 3-(meth)acryloxypropyl trimethoxysilane, 3-(meth)acryloxypropyl triethoxysilane, 2-(meth)acryloxyethyl trichlorosilane, 2-(meth)acryloxyethyl trimethoxysilane, 2-(meth)acryloxyethyl triethoxysilane, 4-(meth)acryloxybutyl trichlorosilane, 4-(meth)acryloxybutyl trimethoxysilane, 4-(meth)acryloxybutyl triethoxysilane, vinyltrichlorosilane, vinyltrimethoxysilane, vinyltriethoxysilane, allyltrichlorosilane, allyltrimethoxysilane, allyltriethoxysilane, methylvinyldichlorosilane, divinyldichlorosilane, divinyldimethoxysilane, chlorovinyldimethylsilane, methoxyvinyldimethylsilane, or a combination of the compounds.

Specific examples of the silane compound (b1) containing a polymerizable unsaturated group preferably include 3-(meth)acryloxypropyl trichlorosilane, 3-(meth)acryloxypropyl trimethoxysilane, vinyltrichlorosilane, vinyltrimethoxysilane, allyltrimethoxysilane, or a combination of the compounds.

Based on a total usage amount of 1.0 mole of the silane compound (b1) containing a polymerizable unsaturated group, the silane compound (b2) containing an epoxy group, and the other silane compounds (b3), the usage amount of the silane compound (b1) containing a polymerizable unsaturated group is 0.2 moles to 1.0 mole, preferably 0.3 moles to 0.9 moles, and more preferably 0.4 moles to 0.8 moles.

In the silane compound of the polysiloxane (B) for polymerization, in the case that the silane compound (b1) containing a polymerizable unsaturated group is not used, the obtained liquid crystal display element has the issue of poor resistance to ultraviolet decay.

Silane Compound (b2) Containing an Epoxy Group

The group containing an epoxy group contained in the silane compound (b2) containing an epoxy group is, for instance, a glycidyl group, a glycidyloxy group, an epoxycyclohexyl group, or an oxetanyl group.

Specifically, the group containing an epoxy group can include at least one of the group represented by formula (2-1), the group represented by formula (2-2), and the group represented by formula (2-3).

The group containing an epoxy group preferably includes at least one of a group represented by formula (2-1-1), a group represented by formula (2-2-2), and a group represented by formula (2-3-1).

Specific examples of the silane compound (b2) containing an epoxy group include 3-(N,N-diglycidyl)aminopropyltrimethoxysilane, 3-(N-allyl-N-glycidyl)aminopropyltrimethoxysilane, 3-glycidoxypropyltrimethoxysilane 3-glycidyloxypropyltrimethoxysilane, 3-glycidoxypropyltriethoxysilane, 3-glycidoxypropylmethyldimethoxysilane, 3-glycidoxypropylmethyldiethoxysilane, 3-glycidoxypropyldimethylmethoxysilane, 3-glycidoxypropyldimethylethoxysilane, 2-glycidoxyethyltrimethoxysilane, 2-glycidoxyethyltriethoxysilane, 2-glycidoxyethylmethyldimethoxysilane, 2-glycidoxyethylmethyldiethoxysilane, 2-glycidoxyethyldimethylmethoxysilane, 2-glycidoxyethyldimethylethoxysilane, 4-glycidoxybutyltrimethoxysilane, 4-glycidoxybutyltriethoxysilane, 4-glycidoxybutylmethyldimethoxysilane, 4-glycidoxybutylmethyldiethoxysilane, 4-glycidoxybutyldimethylmethoxysilane, 4-glycidoxybutyldimethylethoxysilane, 2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane, 2-(3,4-epoxycyclohexyl)ethyltriethoxy silane, 3-(3,4-epoxycyclohexyl)propyltrimethoxysilane, 3-(3,4-epoxycyclohexyl)propyl triethoxysilane, ((3-ethyl-3-oxetanyl)methoxy)propyltrimethoxysilane, ((3-ethyl-3-oxetanyl)methoxy)propyltriethoxysilane, ((3-ethyl-3-oxetanyl)methoxy)propylmethyl dimethoxysilane, ((3-ethyl-3-oxetanyl)methoxy)propyldimethylmethoxysilane, commercial products such as DMS-E01, DMS-E12, DMS-E21, EMS-32 (made by JNC), or a combination of the compounds.

Specific examples of the silane compound (b2) containing an epoxy group preferably include 3-glycidoxypropyltrimethoxysilane, 2-glycidoxyethyltrimethoxy silane, 4-glycidoxybutyltrimethoxysilane, 2-(3,4-epoxycyclohexyl)ethyltrimethoxy silane, 2-(3,4-epoxycyclohexyl)ethyltriethoxysilane, ((3-ethyl-3-oxetanyl)methoxy)propyltrimethoxysilane, ((3-ethyl-3-oxetanyl)methoxy)propyltriethoxysilane, DMS-E01, DMS-E12, or a combination of the compounds.

Based on a total usage amount of 1.0 mole of the silane compound (b1) containing a polymerizable unsaturated group, the silane compound (b2) containing an epoxy group, and the other silane compounds (b3), the usage amount of the silane compound (b2) containing an epoxy group is 0 moles to 0.8 moles, preferably 0.1 moles to 0.7 moles, and more preferably 0.2 moles to 0.6 moles.

Other Silane Compounds (b3)

The other silane compounds (b3) are, for instance, a compound having one silicon atom. The compound having one silicone atom includes a silane compound having four hydrolyzable groups, a silane compound having three hydrolyzable groups, a silane compound having two hydrolyzable groups, a silane compound having one hydrolyzable group, or a combination thereof.

Specific examples of the silane compound having four hydrolyzable groups include tetrachlorosilane, tetramethoxysilane, tetraethoxysilane, tetra-n-propoxysilane, tetraisopropoxysilane, tetra-n-butoxysilane, tetra-sec-butoxysilane, or a combination of the compounds.

Specific examples of the silane compound having three hydrolyzable groups include trichlorosilane, trimethoxysilane, triethoxysilane, fluorotrichlorosilane, fluorotrimethoxysilane, fluorotriethoxysilane, methyl trichlorosilane, methyltrimethoxysilane, methyltriethoxysilane, 2-(trifluoromethyl)ethyltrichlorosilane, 2-(trifluoromethyl)ethyltrimethoxysilane, 2-(trifluoromethyl)ethyltriethoxysilane, hydroxymethyltrichlorosilane, hydroxymethyltrimethoxysilane, hydroxyethyl trimethoxysilane, mercaptomethyltrichlorosilane, 3-mercaptopropyltrichlorosilane, mercaptomethyltrimethoxysilane, mercaptomethyltriethoxysilane, 3-mercaptopropyl trimethoxysilane, 3-mercaptopropyltriethoxysilane, phenyltrichlorosilane, phenyltrimethoxysilane, phenyltriethoxysilane, or a combination of the compounds.

Specific examples of the silane compound having two hydrolyzable groups include methyldichlorosilane, methyldimethoxysilane, methyldiethoxysilane, dimethyldichlorosilane, dimethyldimethoxysilane, dimethyldiethoxysilane, methyl[2-(perfluoro-n-octyl)ethyl]dichlorosilane, methyl[2-(perfluoro-n-octyl)ethyl]dimethoxysilane, 3-mercaptopropylmethyldichlorosilane, 3-mercaptopropylmethyl dimethoxysilane, diphenyldichlorosilane, diphenyldimethoxysilane, or a combination of the compounds.

Specific examples of the silane compound having one hydrolyzable group include chlorodimethylsilane, methoxydimethylsilane, chlorotrimethylsilane, bromotrimethylsilane, iodotrimethylsilane, methoxytrimethylsilane, chloromethyldiphenylsilane, methoxymethyldiphenylsilane, or a combination of the compounds.

Specific examples of commercial products of the other silane compounds (b3) can include, for instance, KC-89, KC-89S, X-21-3153, X-21-5841, X-21-5842, X-21-5843, X-21-5844, X-21-5845, X-21-5846, X-21-5847, X-21-5848, X-22-160AS, X-22-170B, X-22-170BX, X-22-170D, X-22-170DX, X-22-176B, X-22-176D, X-22-176DX, X-22-176F, X-40-2308, X-40-2651, X-40-2655A, X-40-2671, X-40-2672, X-40-9220, X-40-9225, X-40-9227, X-40-9246, X-40-9247, X-40-9250, X-40-9323, X-41-1053, X-41-1056, X-41-1805, X-41-1810, KF6001, KF6002, KF6003, KR212, KR-213, KR-217, KR220 L, KR242A, KR271, KR282, KR300, KR311, KR401N, KR500, KR510, KR5206, KR5230, KR5235, KR9218, KR9706 (made by Shin-Etsu Chemical); glass resin (made by Showa Denko); SH804, SH805, SH806A, SH840, SR2400, SR2402, SR2405, SR2406, SR2410, SR2411, SR2416, SR2420 (made by Dow Corning Toray); FZ3711, FZ3722 (made by NUC); DMS-S12, DMS-S15, DMS-S21, DMS-S27, DMS-S31, DMS-S32, DMS-S33, DMS-S35, DMS-S38, DMS-S42, DMS-545, DMS-551, DMS-227, PSD-0332, PDS-1615, PDS-9931, XMS-5025 (made by JNC); MS51, MS56 (made by Mitsubishi Chemical); and partial condensates of GR100, GR650, GR908, GR950 (made by Showa Denko).

The other silane compounds (b3) are preferably tetramethoxysilane, tetraethoxysilane, methyltrimethoxysilane, methyltriethoxysilane, phenyltrimethoxysilane, phenyltriethoxysilane, 3-mercaptopropyltrimethoxysilane, 3-mercaptopropyltriethoxysilane, mercaptomethyltrimethoxysilane, mercaptomethyl triethoxysilane, dimethyldimethoxysilane, dimethyldiethoxysilane, or a combination of the compounds.

Based on a total usage amount of 1.0 mole of the silane compound (b1) containing a polymerizable unsaturated group, the silane compound (b2) containing an epoxy group, and the other silane compounds (b3), the usage amount of the other silane compounds (b3) is 0 moles to 0.8 moles, preferably 0.1 moles to 0.7 moles, and more preferably 0.2 moles to 0.6 moles.

The polycondensation reaction forming the polysiloxane (B) can include a general method such as adding an organic solvent or water in the silane compound or a mixture thereof, or optionally further adding a catalyst thereto, and then performing heating via, for instance, an oil bath at 50° C. to 150° C., and the heating time is preferably 0.5 hours to 120 hours. During heating, the mixed solution can be stirred, and can also be placed in a reflux condition.

The organic solvent is not particularly limited, and can be the same or different from the solvent (D) contained in the liquid crystal alignment agent of the invention.

Specific examples of the organic solvent include a hydrocarbon compound such as toluene or xylene; a ketone compound such as methyl ethyl ketone, methyl isobutyl ketone, methyl-n-pentyl ketone, diethyl ketone, or cyclohexanone; an ester compound such as ethyl acetate, n-butyl acetate, isopentyl acetate, propylene glycol monomethyl ether acetate, 3-methoxybutyl acetate, or ethyl lactate; an ether compound such as ethylene glycol dimethyl ether, ethylene glycol diethyl ether, tetrahydrofuran, or dioxane; an alcohol compound such as 1-hexanol, 4-methyl-2-pentanol, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol mono-n-propyl ether, ethylene glycol mono-n-butyl ether, propylene glycol monomethyl ether, propylene glycol monoethyl ether, or propylene glycol mono-n-propyl ether, or a combination of the organic solvents.

The organic solvents can be used alone or in multiple combinations.

Based on 100 parts by weight of all of the silane compounds, the usage amount of the organic solvent is preferably 10 parts by weight to 1200 parts by weight, more preferably 30 parts by weight to 1,000 parts by weight.

Based on 1 mole of the hydrolyzable group of all of the silane compounds, the usage amount of water is preferably 0.5 moles to 100 moles, and more preferably 1 mole to 30 moles.

The catalyst is not particularly limited, and the catalyst is preferably selected from an acid, an alkali metal compound, an organic base, a titanium compound, a zirconium compound, or a combination thereof.

Specific examples of the acid include hydrochloric acid, nitric acid, sulfuric acid, hydrofluoric acid, oxalic acid, phosphoric acid, acetic acid, trifluoroacetic acid, formic acid, polybasic carboxylic acid, polybasic acid anhydride, or a combination thereof.

Specific examples of the alkali metal compound include sodium hydroxide, potassium hydroxide, sodium methoxide, potassium methoxide, sodium ethoxide, potassium ethoxide, or a combination thereof.

Specific examples of the organic base include, for instance, a primary or secondary organic amine such as ethylamine, diethylamine, piperazine, piperidine, pyrrolidine, or pyrrole; a tertiary organic amine such as triethylamine, tri-n-propylamine, tri-n-butylamine, pyridine, 4-dimethylaminopyridine, or diazabicycloundecene; a quaternary organic amine such as tetramethylammonium hydroxide, or a combination of the compounds.

The usage amount of the catalyst is different according to, for instance, reaction conditions such as the type or the temperature, and can be suitable set. For instance, based on 1 mole of all of the silane compounds, the additive amount of the catalyst is 0.01 moles to 5 moles, preferably 0.03 moles to 3 moles, and more preferably 0.05 moles to 1 mole.

Based on stability concerns, after the polycondensation reaction is complete, the organic solvent layer fractionated from the reaction solution is preferably washed with water. When washing is performed, water containing a small amount of salt is preferably used, such as performing washing with, for instance, an aqueous solution of around 0.2 wt % ammonium nitrate. The washing can be performed until the washed aqueous layer is neutral, and then after the organic solvent layer is dried via a desiccant such as anhydrous calcium sulfate or a molecular sieve as needed, the organic solvent is removed to obtain polysiloxane (B).

In the polysiloxane (B) of the invention, the polystyrene-equivalent weight average molecular weight obtained according to GPC is 500 to 100,000, preferably 800 to 50,000, and more preferably 1,000 to 20,000.

Based on a usage amount of 100 parts by weight of the polymer (A), the usage amount of the polysiloxane (B) is 1 part by weight to 25 parts by weight, preferably 2 parts by weight to 20 parts by weight, and more preferably 3 parts by weight to 15 parts by weight.

In the case that the polysiloxane (B) is not used in the liquid crystal alignment agent, the liquid crystal display element has the issue of poor resistance to ultraviolet decay.

Polymerizable Compound (C) Containing Benzophenone Structure

The benzophenone structure contained in the polymerizable compound (C) containing a benzophenone structure is at least one selected from the group consisting of formula (3-1) to formula (3-7).

Moreover, the polymerizable compound (C) containing a benzophenone structure can have one or more photoreactive groups. The photoreactive group is a photopolymerizable group or a photo-crosslinkable group, wherein “photopolymerizable group” is a functional group initiating polymerization via light irradiation, and “photo-crosslinkable group” is a functional group which is cross-linked by reacting with the polymer (A) via light irradiation. Moreover, reaction can also occur between “photo-crosslinkable groups”.

It should be mentioned that, the polymerizable compound (C) containing a benzophenone structure preferably has two or more photoreactive groups. When the photoreactive group of the polymerizable compound (C) containing a benzophenone structure used in the liquid crystal alignment agent is two or more, the resistance to ultraviolet decay of the fabricated liquid crystal display element is better.

The photoreactive group contained in the polymerizable compound (C) containing a benzophenone structure is at least one selected from the group consisting of formula (3a) to formula (3d).

In formula (3a) to formula (3d), R1 represents a hydrogen atom or a C1 to C4 alkyl group; Z1 represents a divalent aromatic ring group or a divalent heterocyclic group that may be substituted by a C1 to C12 alkyl group or a C1 to C12 alkoxy group; Z2 represents a monovalent aromatic ring group or a monovalent heterocyclic group that may be substituted by a C1 to C12 alkyl group or a C1 to C12 alkoxy group.

The polymerizable compound (C) containing a benzophenone structure includes a polymerizable compound containing a benzophenone structure having two photopolymerizable groups represented by formula (3-8-1) to formula (3-8-3); a polymerizable compound containing a benzophenone structure having one photopolymerizable group and one photo-crosslinkable group represented by formula (3-9-1) to formula (3-9-4); a polymerizable compound containing a benzophenone structure having two photo-crosslinkable groups represented by formula (3-10-1) to formula (3-10-2), or a combination of the polymerizable compounds.

In formula (3-8-1) to formula (3-8-3), formula (3-9-1) to formula (3-9-4), and formula (3-10-1) to formula (3-10-2), R1, Z1, and Z2 are respectively the same as R1, Z1, and Z2 in formula (3a) to formula (3d), and are not repeated herein. Q1 represents a divalent organic group having a benzophenone structure.

Specific examples of the polymerizable compound containing a benzophenone structure having two photopolymerizable groups represented by formula (3-8-1) to formula (3-8-3) include at least one of the compounds represented by formula (3-11-1) to formula (3-11-6).

In formula (3-11-1) to formula (3-11-6), Y1 represents a single bond or a C1 to C10 straight-chain or branched-chain alkyleneoxy group; Y2 represents a single bond or a C1 to C10 straight-chain or branched-chain alkyleneoxy group; f and g each independently represent 1 or 2; R3 represents a hydrogen atom or a methyl group. Y1 and Y2 can be the same, and can also be different.

Specific examples of the polymerizable compound containing a benzophenone structure having one photopolymerizable group or photo-crosslinkable group include at least one of the compounds represented by formula (3-12-1) to formula (3-12-3).

In formula (3-12-1) to formula (3-12-2), Y1 represents a single bond or a C1 to C10 straight-chain or branched-chain alkyleneoxy group; R3 represents a hydrogen atom or a methyl group. In formula (3-12-3), n2 represents an integer of 2 to 9.

Specific examples of the polymerizable compound containing a benzophenone structure having three or more photopolymerizable groups or photo-crosslinkable groups include a compound represented by formula (3-13).

In formula (3-13), h represents an integer of 3 to 6; Q2 represents a benzophenone structure; R1 is the same as R1 in formula (3a) to formula (3d) and is not repeated herein. In formula (3-13), h number of the structures inside the parentheses bond to Q2, and the structures inside the parentheses may each be the same or different.

In general, during the forming process of the liquid crystal alignment film, to completely remove the solvent, a step of performing baking under high temperature is always contained. In the invention, the polymerizable compound (C) containing a benzophenone structure having a photoreactive group is used instead of a compound having a thermal polymerization structure. As a result, a high-temperature treatment of, for instance, 200° C. or above can be tolerated, thus increasing thermal stability.

The fabrication method of the polymerizable compound (C) containing a benzophenone structure is not particularly limited, and the polymerizable compound (C) containing a benzophenone structure can be synthesized via a method combining synthetic organic chemistry. For instance, the compound containing the photoreactive group of formula (3a) can be synthesized via the methods represented by chemical equation 1 to chemical equation 2 below.

In the above chemical equations, R′ represents a monovalent organic group, and the strongly acidic ion-exchange resin is, for instance, the commercial product Amberlyst 15 (made by Rohm and Haas).

Moreover, the compounds represented by formula (3-11-1) and formula (3-11-2) can be synthesized via chemical equation 3 below. In chemical equation 3, Y1, Y2, and R3 are respectively the same as Y1, Y2, and R3 in formula (3-11-1) and formula (3-11-2), and are not repeated herein. DCC is the abbreviation of dicyclohexylcarbodiimide, and DMAP is the abbreviation of N,N-dimethyl-4-aminopyridine.

The compound represented by formula (3-12-3) can also be synthesized via chemical equation 4 below. In chemical equation 4, n2 represents an integer of 2 to 9.

The polymerizable compound (C) containing a benzophenone structure can be used alone or in multiple combinations.

Based on a usage amount of 100 parts by weight of the polymer (A), the usage amount of the polymerizable compound (C) containing a benzophenone structure is 3 parts by weight to 30 parts by weight, preferably 4 parts by weight to 25 parts by weight, and more preferably 5 parts by weight to 20 parts by weight.

In the case that the polymerizable compound (C) containing a benzophenone structure is not used in the liquid crystal alignment agent, the liquid crystal display element has the issue of mura defect.

Solvent (D)

The solvent used in the liquid crystal alignment agent of the invention is not particularly limited, and only needs to be able to dissolve the polymer (A), the polysiloxane (B), the polymerizable compound (C) containing a benzophenone structure, and any other components without reacting therewith. The solvent is preferably the same as the solvent used in the synthesis of the polyamic acid, and at the same time, the poor solvent used in the synthesis of the polyamic acid can also be used together.

Specific examples of the solvent (D) include, but are not limited to, for instance, N-methyl-2-pyrrolidone (NMP), γ-butyrolactone, γ-butyrolactam, 4-hydroxy-4-methyl-2-pentanone, ethylene glycol monomethyl ether, butyl lactate, butyl acetate, methyl methoxypropionate, ethyl ethoxypropionate, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol n-propyl ether, ethylene glycol isopropyl ether, ethylene glycol n-butyl ether, ethylene glycol dimethyl ether, ethylene glycol ethyl ether acetate, diethylene glycol dimethyl ether, diethylene glycol diethyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, diethylene glycol monomethyl ether acetate, diethylene glycol monoethyl ether acetate, N,N-dimethyl formamide, or N,N-dimethyl acetamide. The solvent (D) can be used alone or in multiple combinations.

Based on a usage amount of 100 parts by weight of the polymer (A), the usage amount of the solvent (D) is 800 parts by weight to 4000 parts by weight, preferably 900 parts by weight to 3500 parts by weight, and more preferably 1000 parts by weight to 3000 parts by weight.

Additive (E)

Without affecting the efficacy of the invention, an additive (E) can further optionally be added to the liquid crystal alignment agent, wherein the additive (E) includes a compound having at least two epoxy groups, a silane compound having a functional group, or a combination thereof.

The compound having at least two epoxy groups includes, but is not limited to, ethylene glycol diglycidyl ether, polyethylene glycol diglycidyl ether, propylene glycol diglycidyl ether, tripropylene glycol diglycidyl ether, polypropylene glycol diglycidyl ether, neopentyl glycol diglycidyl ether, 1,6-hexanediol diglycidyl ether, glycerol diglycidyl ether, 2,2-dibromo-neopentyl glycol diglycidyl ether, 1,3,5,6-tetraglycidyl-2,4-hexanediol, N,N,N′,N′-tetraglycidyl-m-xylenediamine, 1,3-bis(N,N-diglycidylaminomethyl)cyclohexane, N,N,N′,N′-tetraglycidyl-4,4′-diaminodiphenylmethane, N,N-glycidyl-p-glycidyloxy aniline, 3-(N,N-diglycidyl)aminopropyltrimethoxysilane, or a combination of the compounds.

The compound having at least two epoxy groups can be used alone or in multiple combinations.

Based on a usage amount of 100 parts by weight of the polymer (A), the usage amount of the compound having at least two epoxy groups can be 0 parts by weight to 40 parts by weight, preferably 0.1 parts by weight to 30 parts by weight.

Specific examples of the silane compound having a functional group include, but are not limited to, 3-aminopropyltrimethoxysilane, 3-aminopropyltriethoxysilane, 2-aminopropyltrimethoxysilane, 2-aminopropyltriethoxysilane, N-(2-aminoethyl)-3-aminopropyltrimethoxysilane, N-(2-aminoethyl)-3-aminopropyldimethoxysilane, 3-ureidopropyltrimethoxysilane, 3-ureidopropyltriethoxysilane, N-ethoxycarbonyl-3-aminopropyltrimethoxysilane, N-ethoxycarbonyl-3-aminopropyltriethoxysilane, N-triethoxysilylpropyltriethylenetriamine, N-trimethoxysilylpropyltriethylenetriamine, 10-trimethoxysilyl-1,4,7-triazadecane, 10-triethoxysilyl-1,4,7-triazadecane, 9-trimethoxysilyl-3,6-diazanonylacetate, 9-triethoxysilyl-3,6-diazanonylacetate, N-benzyl-3-aminopropyltrimethoxysilane, N-benzyl-3-aminopropyltriethoxysilane, N-phenyl-3-aminopropyltrimethoxysilane, N-phenyl-3-aminopropyltriethoxysilane, N-bis(oxyethylene)-3-aminopropyltrimethoxysilane, N-bis(oxyethylene)-3-aminopropyltriethoxysilane, or a combination of the compounds.

The additive (E) can be used alone or in multiple combinations.

Based on a usage amount of 100 parts by weight of the polymer (A), the usage amount of the silane compound having a functional group can be 0 parts by weight to 10 parts by weight, preferably 0.5 parts by weight to 10 parts by weight.

Based on a total usage amount of 100 parts by weight of the polymer (A), the usage amount of the additive (E) is preferably 0.5 parts by weight to 50 parts by weight, more preferably 1 part by weight to 45 parts by weight.

<Preparation Method of Liquid Crystal Alignment Agent>

The preparation method of the liquid crystal alignment agent of the invention is not particularly limited, and a general mixing method can be used for the preparation. For instance, the polymer (A), the polysiloxane (B), and the polymerizable compound (C) containing a benzophenone structure formed by the above methods are uniformly mixed into a mixture. Then, the solvent (D) is added under the condition of a temperature of 0° C. to 200° C. Next, the additive (E) is optionally added, and lastly the mixture is continuously stirred with a stirring apparatus until dissolved. Moreover, the solvent (D) is preferably added under a temperature of 20° C. to 60° C.

Under 25° C., the viscosity of the liquid crystal alignment agent of the invention is generally 15 cps to 35 cps, preferably 17 cps to 33 cps, and more preferably 20 cps to 30 cps.

<Forming Method of Liquid Crystal Alignment Film>

After the liquid crystal alignment agent of the invention is coated on a substrate, when needed, a coating film obtained via heat treatments such as pre-bake and post-bake is directly used as the liquid crystal alignment film. Moreover, a treatment such as rubbing, or irradiation of, for instance, polarized light or light of a specific wavelength, or an ion beam, can be performed on the coating film. Moreover, ultraviolet is irradiated when voltage is applied to the liquid crystal display element after liquid crystal is filled, so as to form an SCVA film.

At this point, the used substrate only needs to be a substrate having high transparency, and is not particularly limited. The substrate is, for instance, a glass substrate, polycarbonate, poly(meth)acrylate, polyether sulfone, polyarylate, polyurethane, polysulfone, polyether, polyether ketone, trimethyl pentene, polyolefin, polyethylene terephthalate, (meth)acrylonitrile, cellulose triacetate, cellulose diacetate, or cellulose acetate butyrate. From the perspective of a simplified process, the substrate is preferably a substrate on which, for instance, an indium tin oxide (ITO) electrode for driving a liquid crystal is formed. Moreover, in the case that the reflective liquid crystal display element is a one-sided substrate, an opaque object such as a silicon wafer can also be used. Moreover, the electrode in this case can also include a light-reflecting material such as aluminum.

The coating method of the liquid crystal alignment agent is not particularly limited, and is, for instance, a printing method such as screen printing, offset printing, or flexo printing, an ink jet method, a spray coating method, a roll coating method, immersion, slit coating, or spin coating. From the perspective of productivity, the widely industrially used transfer printing is also suitable for the invention.

After the liquid crystal alignment agent is coated via the above method, a coating film is formed via a pre-bake treatment and a post-bake treatment. Although the pre-bake step after the liquid crystal alignment agent is coated is not required, when the time between the coating and the post-bake is not fixed for each substrate, or when the post-bake is not performed immediately after the coating, a pre-bake step is preferably further performed. The only condition for the pre-bake step is that the organic solvent is volatilized without deforming the shape of the coating film due to, for instance, transport of the substrate. The conditions of the pre-bake treatment are not particularly limited, and the pre-bake treatment is, for instance, performed under any temperature of 40° C. to 150° C., preferably 50° C. to 120° C., and more preferably 60° C. to 100° C. The pre-bake treatment can be performed for any time from 0.1 minutes to 30 minutes, preferably performed for 0.5 minutes to 15 minutes, and more preferably performed for 1 minute to 5 minutes.

The conditions of the post-bake treatment are not particularly limited, and the post-bake treatment is, for instance, performed under any temperature of 100° C. to 350° C., preferably 120° C. to 300° C., and more preferably 150° C. to 250° C. The post-bake treatment can be performed for any time from 5 minutes to 240 minutes, preferably performed for 10 minutes to 100 minutes, and more preferably performed for 20 minute to 90 minutes. The heating can be performed via a known method, and can be performed via, for instance, a heating plate, a convection oven, or an infrared furnace.

The thickness of the liquid crystal alignment film obtained after post-bake is not particularly limited, and can be, for instance, 1 nm to 1000 nm, preferably 5 nm to 500 nm, and more preferably 10 nm to 300 nm.

<Liquid Crystal Display Element and Fabrication Method Thereof>

The liquid crystal display element of the invention includes the liquid crystal alignment film formed by the liquid crystal alignment agent of the invention. The liquid crystal display element of the invention can be fabricated according to the following method.

Specifically, the liquid crystal display element of the invention can be obtained by fabricating a liquid crystal cell via a known method after a liquid crystal alignment film is formed on a substrate via the above method. Specific examples of the liquid crystal display element include, for instance, a vertical alignment-type liquid crystal display element provided with a liquid crystal cell, wherein the liquid crystal cell has: two substrates disposed opposite to each other, a liquid crystal layer disposed between the substrates, and the liquid crystal alignment film formed by the liquid crystal alignment agent of the invention and disposed between the substrates and the liquid crystal layer.

Specifically, in the vertical alignment-type liquid crystal display element provided with a liquid crystal cell, the liquid crystal cell is fabricated via the following method: the liquid crystal alignment agent of the invention is coated on two substrates, and then a liquid crystal alignment film is formed via pre-bake and post-bake. Then, the two substrates are disposed in a manner in which the liquid crystal alignment films are facing to each other. The liquid crystal layer formed by a liquid crystal is clamped between the two substrates, wherein the liquid crystal layer is disposed in contact with the liquid crystal alignment film. Lastly, voltage is applied to the liquid crystal alignment film and the liquid crystal layer, and ultraviolet is irradiated at the same time.

Voltage is applied to the liquid crystal alignment film formed by the liquid crystal alignment agent of the invention and the liquid crystal layer, and ultraviolet is irradiated at the same time to perform polymerization on the polymerizable compound. At the same time, the polymerizable unsaturated groups of the polysiloxane are reacted with one another, or the polymerizable unsaturated groups are reacted with the polymerizable compound, such that the alignment of the liquid crystal is more efficiently fixed. As a result, a liquid crystal display element having good resistance to ultraviolet decay and no mura defect is formed.

The method of clamping the liquid crystal layer between the two substrates includes, for instance, the following two known methods:

(Method 1)

A pair of substrates on which a liquid crystal alignment film is each formed are prepared, and a spacer such as a bead is spread on the liquid crystal alignment film of one of the substrates. Then, the two liquid crystal alignment films are adhered to another substrate in a manner in which the liquid crystal alignment films are facing to each other, and then liquid crystal is injected under reduced pressure. Lastly, sealing is performed.

(Method 2)

A pair of substrates on which a liquid crystal alignment film is each formed are prepared, and after a spacer such as a bead is spread on the liquid crystal alignment film of one of the substrates, liquid crystal is dropped, then the two liquid crystal alignment films are adhered to another substrate in a manner in which the liquid crystal alignment films are facing to each other, and then sealing is performed.

In the two methods, the thickness of the spacer is preferably 1 μm to 30 μm, more preferably 2 μm to 10 μm.

The step in which voltage is applied to the liquid crystal alignment film and the liquid crystal layer while irradiating ultraviolet to fabricate a liquid crystal cell includes, for instance, applying the voltage between electrodes disposed on a substrate to apply an electric field to the liquid crystal alignment film and the liquid crystal layer, and irradiating ultraviolet while maintaining the electric field. In particular, the voltage applied between the electrodes is, for instance, 5 Vp-p to 30 Vp-p, preferably 5 Vp-p to 20 Vp-p. The amount of ultraviolet irradiation is, for instance, 1 J to 60 J, preferably 40 J or less, and more preferably 10 J or less. The less the amount of ultraviolet irradiation, the more poor reliability generated by damage to the liquid crystal or the material forming the liquid crystal display element can be inhibited. Moreover, by reducing the time of ultraviolet irradiation, the fabrication efficiency can be increased. In the invention, even a lesser amount of ultraviolet irradiation can also increase response speed, and therefore even with a low irradiation amount such as 5 J, a liquid crystal display element having sufficiently fast response speed can also be formed.

Accordingly, when voltage is applied to the liquid crystal alignment film and the liquid crystal layer while irradiating ultraviolet, the polymerizable compound can be reacted to form a polymer. In addition, the polymerizable unsaturated groups of the polysiloxane can also be reacted with one other during ultraviolet irradiation, or be reacted with the polymerizable compound. Via the above reaction, the liquid crystal alignment film can obtain a better cured structure, such that the obtained liquid crystal display element has the characteristics of good resistance to ultraviolet decay and no mura defect.

Moreover, not only can the liquid crystal alignment agent be used for the fabrication of a vertical-alignment type liquid crystal display element such as an SCVA-type liquid crystal display, but is also suitable for the application of a liquid crystal alignment film fabricated via a rubbing treatment or an optical alignment treatment.

The liquid crystal includes, for instance, a nematic liquid crystal or a smectic liquid crystal. Specific examples of the liquid crystal include, but are not limited to, a liquid crystal having positive dielectric anisotropy, and examples thereof can include, for instance, a biphenyl-based liquid crystal, a phenyl cyclohexane-based liquid crystal, an ester-based liquid crystal, a terphenyl-based liquid crystal, a biphenyl cyclohexane-based liquid crystal, a pyrimidine-based liquid crystal, a dioxane-based liquid crystal, a bicyclooctane-based liquid crystal, a cubane-based liquid crystal, or a combination of the liquid crystals. Moreover, the following can further be added to the liquid crystal above: a cholesteric liquid crystal such as cholesteryl chloride, cholesteryl nonanoate, or cholesteryl carbonate . . . etc.; a chiral agent sold under the product name of, for instance, “C-15” or “CB-15” (made by Merck & Co.); or a ferroelectric liquid crystal such as p-decyloxybenzylidene-p-amino-2-methyl butyl cinnamate.

Moreover, specific examples of the liquid crystal can also include a liquid crystal having negative dielectric anisotropy, and examples thereof can include, for instance, a dicyanobenzene-based liquid crystal, a pyridazine-based liquid crystal, a Schiff base-based liquid crystal, an azoxy-based liquid crystal, a biphenyl-based liquid crystal, a phenyl cyclohexane-based liquid crystal, or a combination of the liquid crystals.

The following examples are used to further describe the invention. However, it should be understood that, the examples are only exemplary, and are not intended to limit the implementation of the invention.

Synthesis Examples of Polymer (A)

In the following, synthesis example A-1-1 to synthesis example A-1-5 of the polymer (A) are described:

Synthesis Example A-1-1

A nitrogen inlet, a stirrer, a condenser tube, and a thermometer were provided to a four-necked flask having a volume of 500 mL, and then nitrogen gas was introduced. Then, in the four-necked flask, 4.86 g (0.045 moles) of p-diaminobenzene (hereinafter a2-1), 1.91 g (0.005 moles) of a diamine compound represented by formula (II-12) (hereinafter a2-4), and 80 g of N-methyl-2-pyrrolidone (hereinafter NMP) were added, and the mixture was stirred under room temperature until dissolved. Next, 9.80 g (0.05 mol) of 1,2,3,4-cyclobutane tetracarboxylic dianhydride (a1-1 hereinafter) and 20 g of NMP were added, and the mixture was reacted at room temperature for 2 hours. After the reaction was complete, the reaction solution was poured into 1500 ml of water to precipitate a polymer. Then, the obtained polymer was filtered and was repeatedly washed with methanol and filtered three times. The polymer was then placed in a vacuum oven and dried at a temperature of 60° C., thereby obtaining polymer (A-1-1).

Synthesis Example A-1-2 to Synthesis Example A-1-5

Polymer (A-1-2) to polymer (A-1-5) of synthesis example A-1-2 to synthesis example A-1-5 were respectively prepared with the same steps as synthesis example A-1-1, and the difference thereof is: the types and the usage amounts of the monomers were changed (as shown in Table 1).

In the following, synthesis example A-2-1 to synthesis example A-2-10 of the polymer (A) are described:

Synthesis Example A-2-1

A nitrogen inlet, a stirrer, a condenser tube, and a thermometer were provided to a four-necked flask having a volume of 500 mL, and then nitrogen gas was introduced. Then, in the four-necked flask, 4.86 g (0.045 moles) of p-diaminobenzene (hereinafter a2-1), 1.91 g (0.005 moles) of a diamine compound represented by formula (II-12) (hereinafter a2-4), and 80 g of N-methyl-2-pyrrolidone (hereinafter NMP) were added, and the mixture was stirred under room temperature until dissolved. Next, 9.80 g (0.05 moles) of 1,2,3,4-cyclobutane tetracarboxylic dianhydride (a1-1 hereinafter) and 20 g of NMP were added. After the mixture was reacted at room temperature for 6 hours, 97 g of NMP, 2.55 g of acetic anhydride, and 19.75 g of pyridine were added. Then, the temperature was raised to 60° C., and the mixture was continuously stirred for 2 hours to perform an imidization reaction. After the reaction was complete, the reaction solution was poured into 1500 ml of water to precipitate a polymer. Then, the obtained polymer was filtered and was repeatedly washed with methanol and filtered three times. The polymer was then placed in a vacuum oven and dried at a temperature of 60° C., thereby obtaining polymer (A-2-1).

Synthesis Example A-2-2 to Synthesis Example A-2-10

Polymer (A-2-2) to polymer (A-2-10) of synthesis example A-2-2 to synthesis example A-2-10 were respectively prepared with the same steps as synthesis example A-2-1, and the difference thereof is: the types and the usage amounts of the monomers were changed (as shown in Table 1).

The compounds corresponding to the abbreviations in Table 1 are as shown below.


Abbreviation
Component
a1-1
1,2,3,4-cyclobutane tetracarboxylic dianhydride
a1-2
Pyromellitic dianhydride
a1-3
2,3,5-tricarboxycyclopentylacetic dianhydride
a1-4
3,4-dicarboxy-1,2,3,4-tetrahydronaphthalene-1-succinic dianhydride
a2-1
p-diaminobezene
a2-2
4,4′-diaminodiphenylmethane
a2-3
4,4′-diaminodiphenyl ether
a2-4
Diamine compound represented by formula (II-12)
formula (II-12)
a2-5
Diamine compound represented by formula (II-22)
formula (II-22)
a2-6
1-octadecoxy-2,4-diaminobenzene
a2-7
Diamine compound represented by formula (II-1-4)
formula (II-1-4)
a2-8
Diamine compound represented by formula (II-28)
formula (II-28)
a2-9
Diamine compound represented by formula (II-30)
formula (II-30)


TABLE 1
Component
Synthesis example
(unit: mole %)
A-1-1
A-1-2
A-1-3
A-1-4
A-1-5
A-2-1
A-2-2
A-2-3
A-2-4
A-2-5
A-2-6
A-2-7
A-2-8
A-2-9
A-2-10
Tetra-
a1-1
100
100
80
100
carboxylic
a1-2
100
50
100
50
20
100
dianhydride
a1-3
100
100
100
70
component
a1-4
100
50
100
50
30
(a1)
Diamine
a2-1
90
94
90
94
60
75
80
component
a2-2
85
90
85
90
25
92
15
88
(a2)
a2-3
85
15
85
15
5
a2-4
10
5
10
15
10
6
a2-5
6
6
a2-6
10
10
6
a2-7
5
10
a2-8
15
5
4
a2-8
5
4
Imidization ratio
0
0
0
0
0
15
20
26
30
42
55
68
73
90
95
(%)

Synthesis Examples of Polysiloxane (B)

Synthesis example B-1 to synthesis example B-6 of the polysiloxane (B) are described below.

Synthesis Example B-1

A stirrer, a condenser tube, and a thermometer were provided to a three-necked flask having a volume of 500 mL. Then, in the three-necked flask, 0.4 moles of 3-acryloxypropyltrimethoxysilane (hereinafter GAPTS), 0.5 moles of methyltrimethoxysilane (hereinafter MTMS), 0.1 moles of phenyltrimethoxysilane (hereinafter PTMS), and 6 g of propylene glycol monomethyl ether (hereinafter PGME) were added, and an aqueous solution (20 g triethylamine (hereinafter TEA)/200 g H2O) of TEA was added within 30 minutes while the mixture was stirred under room temperature. Then, the three-necked flask was immersed in an oil bath at 30° C. and stirred for 30 minutes, and then the temperature of the oil bath was raised to 90° C. within 30 minutes. When the internal temperature of the solution reached 75° C., the mixture was continuously heated and stirred to perform polycondensation for 6 hours. After the reaction was complete, the organic layer was removed and washed with an aqueous solution of 0.2 wt % ammonium nitrate to obtain polysiloxane (B-1).

Synthesis Example B-2 to Synthesis Example B-6

Polysiloxane (B-2) to polysiloxane (B-6) of synthesis example B-2 to synthesis example B-6 were prepared with the same steps as synthesis example B-1, and the difference thereof is: the types and the usage amounts of the reactants of the polysiloxane (B) were changed, the types and the usage amounts of the catalysts and the solvents were changed, and the reaction temperatures and the polycondensation times were changed (as shown in Table 2).

Synthesis Example B′-1 to Synthesis Example B′-3

Polysiloxane (B′-1) to polysiloxane (B′-3) of synthesis example B′-1 to synthesis example B′-3 were prepared with the same steps as synthesis example B-1, and the difference thereof is: the types and the usage amounts of the reactants of the polysiloxane (B) were changed, the types and the usage amounts of the catalysts and the solvents were changed, and the reaction temperatures and the polycondensation times were changed (as shown in Table 2).

The compounds corresponding to the abbreviations in Table 2 are as shown below.

ABBREVIATION COMPOUND

  • GMPTS 3-methacryloxypropyltrimethoxy silane
  • GAPTS 3-acryloxypropyltrimethoxy silane
  • VTMS Vinyltrimethoxy silane
  • ATMS Allyltrimethoxysilane
  • GETMS 2-glycidoxyethyltrimethoxy silane
  • GBTMS 4-glycidoxybutyltrimethoxysilane
  • ECETS 2-(3,4-epoxycyclohexyl)ethyltrimethoxy silane
  • ECEES 2-(3,4-epoxycyclohexyl)ethyltriethoxysilane
  • OXTMS (3-ethyl-3-oxetanyl)methoxy)propyltrimethoxysilane
  • OXTES (3-ethyl-3-oxetanyl)methoxy)propyltriethoxysilane
  • MTMS Methyltrimethoxy silane
  • DMDMS Dimethyldimethoxy silane
  • PTMS Phenyltrimethoxy silane
  • PTES Phenyltriethoxy silane
  • PGME Propylene glycol mono methyl ether
  • MIBK Methyl isobutyl ketone
  • H2O Water
  • TEA Triethylamine


TABLE 2
Component
Synthesis example
(unit: mole)
B-1
B-2
B-3
B-4
B-5
B-6
B-7
B′-1
B′-2
B′-3
Silane compound
GMPTS
0.5
0.2
(b1) containing a
GAPTS
0.4
0.2
1
polymerizable
VTMS
0.6
0.1
0.25
unsaturated
ATMS
0.2
group
Silane compound
GETMS
0.8
0.8
(b2) containing
GBTMS
0.5
0.5
an epoxy group
ECETS
0.1
ECEES
0.1
OXTMS
0.1
OXTES
0.1
Other silane
MTMS
0.5
0.2
0.2
0.2
0.5
compounds
DMDMS
0.3
0.45
(b3)
PTMS
0.1
0.1
PTES
0.2
0.1
0.3
0.4
Solvent (g)
PGME
6
8
6
8
9
6
MIBK
6
8
2
6
8
Catalyst (g)
H2O
200
200
250
220
250
200
230
200
200
250
TEA
20
20
22
20
25
20
20
20
20
25
Reaction temperature (° C.)
75
70
80
75
85
70
65
75
80
70
Polycondensation time
6
6.5
6
6
5
7
8
6
6
7
(hours)

Synthesis Examples of Polymerizable Compound (C) Containing Benzophenone Structure

Synthesis example C-1 to synthesis example C-6 of the polymerizable compound (C) containing a benzophenone structure are described below:

Synthesis Example C-1

The synthesis steps of the polymerizable compound containing a benzophenone structure of synthesis example C-1 (hereinafter “polymerizable compound (C-1) containing a benzophenone structure”) are as follows.

(1) Synthesis of Compound C-1a

7.65 g (0.05 moles) of methyl 4-hydroxybenzoate, 9.2 g (0.05 moles) of 6-bromo-1-hexanol, 13.8 g (0.1 moles) of potassium carbonate, and 85 mL of acetone were added to a 200 mL eggplant-shaped flask provided with a condenser tube, and the mixture was stirred and reacted under 65° C. for 24 hours. After the reaction was complete, the solvent was removed via filtering under reduced pressure to obtain a yellow moist solid. Purification was performed on the moist solid via a silica gel column chromatography method (column: silica gel 60, 0.063 mm to 0.200 mm, made by Merck & Co., eluent: hexane/ethyl acetate=1/1 (v/v)) to obtain 11.2 g of compound C-1a.

(2) Synthesis of Compound C-1b

2.2 g (0.01 moles) of pyridinium chlorochromate (hereinafter PCC) and 15 mL of CH2Cl2 were added to a 100 mL three-necked flask provided with a condenser tube. While the components were stirred and mixed, a CH2Cl2 solution containing the obtained compound C-1a (compound C-1a/CH2Cl2=2.5 g/15 mL) was added dropwise, and the mixture was stirred under room temperature for 8 hours. Then, after the oily substance attached to the wall of the flask was removed, 95 mL of diethyl ether was added in the solution, and the solvent was removed via filtering under reduced pressure to obtain a dark green moist solid. Purification was performed on the moist solid via a silica gel column chromatography method (column: silica gel 60, 0.063 mm to 0.200 mm, made by Merck & Co., eluent: hexane/ethyl acetate=2/1 (v/v)) to obtain 1.28 g of compound C-1b.

(3) Synthesis of Compound C-1c

1.25 g (0.005 moles) of the obtained compound C-1b, 0.85 g (0.005 moles) of 2-(bromomethyl)acrylic acid, 0.82 g of Amberlyst 15 (made by Rohm and Haas, product name), 8 mL of tetrahydrofuran (hereinafter THF), 0.95 g (0.005 moles) of tin (II) chloride, and 3 mL of pure water were added in a 50 mL eggplant-shaped flask provided with a condenser tube, and the mixture was stirred and reacted under 70° C. for 6 hours. After the reaction was complete, the reaction solution was filtered under reduced pressure, then 50 mL of pure water was added, and then 50 mL of diethyl ether was used to perform extraction three times. Lastly, the extracted organic layer was dried by using magnesium sulfate, then filtering was performed, and then the solvent was removed via an evaporator to obtain 1.5 g of compound C-1c.

(4) Synthesis of Compound C-1d

40 mL of ethanol, 1.5 g (0.0047 moles) of the obtained compound C-1c, and 5 mL of an aqueous solution of 10% sodium hydroxide were added in a 100 mL eggplant-shaped flask provided with a condenser tube, and the mixture was stirred and reacted under 85° C. for 5 hours. After the reaction was complete, the reaction solution was poured into a 500 mL beaker, then 300 mL of water was added, and then the mixture was stirred under room temperature for 30 minutes. Then, 5 mL of an aqueous solution of 10% hydrochloric acid was added dropwise, and after filtering, 1.36 g of a white solid was obtained.

1.15 g of the obtained white solid, 1 g of Amberlyst 15, and 30 mL of THF were added in a 50 mL of eggplant-shaped flask provided with a condenser tube, and then the mixture was stirred and reacted under 70° C. for 5 hours. After the reaction was complete, the reaction solution was filtered under reduced pressure, and then the solvent was removed via an evaporator to obtain a yellow solid. Lastly, recrystallization was performed by using a mixed solution of ethyl acetate/hexane (v/v=1/1) to obtain 0.93 g of compound C-1d.

(5) Synthesis of Polymerizable Compound (C-1) Containing Benzophenone Structure

3.05 g of the obtained compound C-1d (0.01 moles), 1.98 g of 4-hydroxybenzophenone (0.01 moles), 0.1 g of N,N-dimethyl-4-aminopyridine (hereinafter DMAP), and a small amount of 2,6-di-tert-butyl-p-cresol (hereinafter BHT) were stirred under room temperature, and then 80 mL of CH2Cl2 was added to form a suspension. Then, a CH2Cl2 solution in which dicyclohexyl carbodiimide (hereinafter DCC) was dissolved (DCC/CH2Cl2=5.2 g/15 mL) was added, and then the mixture was continuously stirred to slowly form a precipitate. After 12 hours, the precipitate was filtered, and the filtrate was independently washed twice via 50 mL of 0.5N hydrochloric acid, 50 mL of an aqueous solution of saturated sodium bicarbonate, and 120 mL of saturated salt water in order. Then, drying was performed via magnesium sulfate, and then the solvent was removed under reduced pressure. Lastly, after purification by recrystallization was performed via ethanol, 3.9 g of polymerizable compound (C-1) containing a benzophenone structure was obtained.

Synthesis Example C-2

The polymerizable compound containing a benzophenone structure of synthesis example C-2 (hereinafter “polymerizable compound (C-2) containing a benzophenone structure”) was synthesized according to the following synthesis route 2.

18.4 g of 4-hydroxy benzophenone (compound C-2a, 0.093 moles), 24.5 g of triethylamine (hereinafter TEA, 0.24 moles), and 250 g of THF were added in a four-necked flask having a volume of 1000 mL. After nitrogen substitution, the reaction solution was cooled to 10° C. or less, and a THF solution of methacryloyl chloride (hereinafter MAC) (MAC/THF=14.7 g/30 g) was added dropwise while noting heat generation. After the dropwise addition was complete, the reaction solution was restored to 23° C. and stirred again. After the reaction was complete, the reaction solution was injected into 2500 mL of distilled water. Then, the precipitated solid was filtered and washed via distilled water and methanol in order, and then after drying under reduced pressure, 20.9 g of polymerizable compound (C-2) containing a benzophenone structure was obtained.

Synthesis Example C-3

The polymerizable compound containing a benzophenone structure of synthesis example C-3 (hereinafter “polymerizable compound (C-3) containing a benzophenone structure”) was synthesized according to the following synthesis route 3.

In a four-necked flask having a volume of 1000 mL, 20 g of 4,4′-dihydroxybenzophenone (compound C-3a, 0.093 moles), 58.2 g of the compound C-3b (0.465 moles), 77.38 g of potassium carbonate (0.56 moles), and 300 g of N,N′-dimethylformamide (hereinafter DMF) were added in a four-necked flask having a volume of 1000 mL. After nitrogen substitution, the mixture was heated and stirred at 100° C. After the reaction was complete, the reaction solution was injected into 5000 mL of distilled water, and then the precipitated solid was filtered and washed via distilled water and methanol in order. Lastly, after drying under reduced pressure, 26.18 g of compound C-3c was obtained.

26.14 g of the compound C-3c (0.086 moles) obtained above, 22.7 g of TEA (0.22 moles), and 300 g of THF were added in a four-necked flask having a volume of 1000 mL. After nitrogen substitution, the reaction solution was cooled to 10° C. or less, and a THF solution of MAC (MAC/THF=27.15 g/100 g) was added dropwise while noting heat generation. After the dropwise addition, the reaction solution was restored to 23° C. and stirred again. After the reaction was complete, the reaction solution was injected into 2500 mL of distilled water, and extraction was performed via a mixed solution of ethyl acetate/hexane (v/v=1/1). Then, the organic layer was washed via salt water three times, and then the organic layer was dried by using magnesium sulfate. Then, filtering was performed, and then the solvent was removed via an evaporator. Then, 100 g of 2-propanol was added, and after the 2-propanol was stirred under room temperature and crystallized, filtering and drying under reduced pressure were performed to obtain 10.15 g of polymerizable compound (C-3) containing a benzophenone structure.

Synthesis Example C-4

The polymerizable compound containing a benzophenone structure of synthesis example C-4 (hereinafter “polymerizable compound (C-4) containing a benzophenone structure”) was synthesized according to the following synthesis route 4.

20 g of 4,4-dihydroxybenzophenone (compound C-3a, 0.093 moles), 24.5 g of TEA (0.24 moles), and 250 g of THF were added in a four-necked flask having a volume of 1000 mL. After nitrogen substitution, the reaction solution was cooled to 10° C. or less, and a THF solution of MAC (MAC/THF=29.4 g/50 g) was added dropwise while noting heat generation. After the dropwise addition was complete, the reaction solution was restored to 23° C. and stirred again. After the reaction was complete, the reaction solution was injected into 2500 mL of distilled water. Then, the precipitated solid was filtered and washed via distilled water and methanol in order, and then after drying under reduced pressure, 27.5 g of polymerizable compound (C-4) containing a benzophenone structure was obtained.

Synthesis Example C-5

The polymerizable compound containing a benzophenone structure of synthesis example C-5 (hereinafter “polymerizable compound (C-5) containing a benzophenone structure”) was synthesized according to the following synthesis route 5.

25 g of the compound C-5a (0.10 moles), 95.5 g of the compound C-5b (0.045 moles), 113 g of potassium carbonate (0.81 moles), and 325 g of DMF were added in a four-necked flask having a volume of 1000 mL. After nitrogen substitution, heating and stirring were performed at 100° C. After the reaction was complete, the reaction solution was injected into 2300 mL of distilled water, and extraction was performed by adding a mixed solution of ethyl acetate/hexane (v/v=1/1). Then, the organic layer was washed via salt water three times, and then the organic layer was dried by using magnesium sulfate. Then, filtering was performed, and then the solvent was removed via an evaporator. Then, 750 g of ethanol and 1000 g of an aqueous solution of 10 wt % sodium hydroxide solution were added, and then the mixture was heated and stirred under 85° C. After the reaction was complete, the reaction solution was injected into 900 g of an aqueous solution of 10 wt % hydrochloric acid, and then the precipitated solid was filtered and washed via distilled water, methanol, and ethyl acetate in order. Lastly, after drying under reduced pressure, 59 g of compound C-5c was obtained.

59 g of the compound C-5c (0.099 moles) obtained above, 47.8 g of TEA (0.47 moles), and 800 g of THF were added in a four-necked flask having a volume of 2000 mL. After nitrogen substitution, the reaction solution was cooled to 10° C. or less, and a THF solution of MAC (MAC/THF=59 g/100 g) was added dropwise while noting heat generation. After the dropwise addition was complete, the reaction solution was restored to 23° C. and stirred again. After the reaction was complete, the reaction solution was injected into 3700 mL of distilled water, and extraction was performed by using ethyl acetate. Then, the organic layer was washed via an aqueous solution of 20 wt % potassium carbonate and salt water in order three times, and then the organic layer was dried by using magnesium sulfate. Then, filtering was performed, and then the solvent was removed via an evaporator to obtain 70.6 g of polymerizable compound (C-5) containing a benzophenone structure.

Synthesis Example C-6

The synthesis steps of the polymerizable compound containing a benzophenone structure of synthesis example C-6 (hereinafter “polymerizable compound (C-6) containing a benzophenone structure”) are as follows.

(1) Synthesis of Compound C-6a

7.65 g of methyl 4-hydroxybenzoate (0.05 moles), 9 g of 6-bromo-1-hexanol (0.05 moles), 13.8 g of potassium carbonate (0.1 moles), and 90 mL of acetone were added in a 200 mL eggplant-shaped flask provided with a condenser tube, and then the mixture was stirred and reacted under 65° C. for 24 hours. After the reaction was complete, the solvent was removed via filtering under reduced pressure to obtain a yellow moist solid. Purification was performed on the moist solid via a silica gel column chromatography method (column: silica gel 60, 0.063 mm to 0.200 mm, made by Merck & Co., eluent: hexane/ethyl acetate=1/1 (v/v)) to obtain 11.2 g of compound C-6a.

(2) Synthesis of Compound C-6b

2.2 g of PCC (0.01 moles) and 15 mL of CH2Cl2 were added in a 100 mL three-necked flask provided with a condenser tube. While the components were stirred and mixed, a CH2Cl2 solution containing the obtained compound C-6a (C-6a/CH2Cl2=2.5 g/15 mL) was added dropwise, and the mixture was stirred under room temperature for 6 hours. Then, after the oily substance attached to the wall of the flask was removed, 90 mL of diethyl ether was added in the solution, and the solvent was removed via filtering under reduced pressure to obtain a dark green moist solid. Purification was performed on the moist solid via a silica gel column chromatography method (column: silica gel 60, 0.063 mm to 0.200 mm, made by Merck & Co., eluent: hexane/ethyl acetate=2/1 (v/v)) to obtain 1.3 g of compound C-6b.

(3) Synthesis of Compound C-6c

1.25 g of the obtained compound C-6b (0.005 moles), 0.85 g of 2-(bromomethyl)acrylic acid (0.005 moles), 0.82 g of Amberlyst 15, 8 mL of THF, 0.95 g of tin (II) chloride (0.005 moles), and 3 mL of pure water were added in a 50 mL eggplant-shaped flask provided with a condenser tube, and then the mixture was stirred and reacted under 70° C. for 5 hours. After the reaction was complete, the reaction solution was filtered under reduced pressure, then 50 mL of pure water was added, and then 50 mL of diethyl ether was used to perform extraction three times. Lastly, drying was performed on the extracted organic layer by using magnesium sulfate, then filtering was performed, and then the solvent was removed via an evaporator to obtain 1.5 g of compound C-6c.

(4) Synthesis of Compound C-6d

40 mL of ethanol, 1.52 g of the obtained compound C-6c (0.0047 moles), and 5 mL of an aqueous solution of 10% sodium hydroxide were added in a 100 mL eggplant-shaped flask provided with a condenser tube, and then the mixture was stirred and reacted under 85° C. for 3 hours. After the reaction was complete, the reaction solution was poured into a 500 mL beaker, then 300 mL of water was added, and then the mixture was stirred under room temperature for 30 minutes. Then, 5 mL of an aqueous solution of 10% hydrochloric acid was added dropwise, and after filtering, 1.3 g of a white solid was obtained.

1.1 g of the obtained white solid, 1 g of Amberlyst 15, and 25 mL of THF were added in a 50 mL of eggplant-shaped flask provided with a condenser tube, and then the mixture was stirred and reacted under 70° C. for 5 hours. After the reaction was complete, the reaction solution was filtered under reduced pressure, and then the solvent was removed via an evaporator to obtain a yellow solid. Lastly, recrystallization was performed on a mixed solution of ethyl acetate/hexane (v/v=1/1) to obtain 0.92 g of compound C-6d.

(5) Synthesis of Polymerizable Compound (C-6) Containing Benzophenone Structure

6.3 g of the compound C-6d (0.02 moles) obtained above, 2.2 g of 4,4′-dihydroxybenzophenone (0.01 moles), 0.1 g of DMAP, and a small amount of BHT were stirred under room temperature, and then 80 mL of CH2Cl2 was added to form a suspension. Then, a CH2Cl2 solution (DCC/CH2Cl2=5.2 g/15 mL) in which DCC was dissolved was added, and then the mixture was continuously stirred to slowly form a precipitate. After 12 hours, the precipitate was filtered, and the filtrate was independently washed twice via 50 mL of 0.5 N hydrochloric acid, 50 mL of an aqueous solution of saturated sodium bicarbonate, and 120 mL of saturated salt water in order. Then, drying was performed via magnesium sulfate, and then the solvent was removed under reduced pressure. Lastly, after purification by recrystallization was performed by using ethanol, 6.15 g of polymerizable compound (C-6) containing a benzophenone structure was obtained.

Examples and Comparative Examples of Liquid Crystal Alignment Agent, Liquid Crystal Alignment Film, and Liquid Crystal Display Element

Example 1 to example 15 and comparative example 1 to comparative example 14 of the liquid crystal alignment agent, the liquid crystal alignment film, and the liquid crystal display element are described below:

Example 1

a. Liquid Crystal Alignment Agent

100 parts by weight of the polymer (A-1-1), 5 parts by weight of the polysiloxane (B-1), 8 parts by weight of the polymerizable compound (C-1) containing a benzophenone structure, 1200 parts by weight of N-methyl-2-pyrrolidone (D-1 hereinafter), and 1200 parts by weight of ethylene glycol n-butyl ether (D-2 hereinafter) were weighed. Then, the components were continuously stirred under room temperature with a stirring apparatus until dissolved to form the liquid crystal alignment agent of example 1.

b. Liquid Crystal Alignment Film and Liquid Crystal Display Element

A liquid crystal cell was fabricated via the order shown below by using the obtained liquid crystal alignment agent. The liquid crystal alignment agent was respectively coated on two glass substrates each having an ITO electrode via a spin coating method, wherein the ITO electrodes were respectively a slit pattern having a line/space of 5 μm. Then, after pre-baking at 80° C. for 2 minutes on a heating plate, post-bake was performed in a circulation oven at 220° C. for 20 minutes to form the liquid crystal alignment film of example 1.

A thermal adhesive was coated on one of the two glass substrates on which a liquid crystal alignment film was each formed, and a 4 μm spacer was distributed in the other one. Next, the two glass substrates were pressed, and a pressure of 10 kg was applied with a hot press machine to perform hot press lamination under the condition of a temperature of 150° C. Then, after liquid crystal was injected via a liquid crystal injection machine (made by Shimadzu Corporation, model: ALIS-100X-CH), the liquid crystal injection hole was sealed via an ultraviolet curing sealant, and then the ultraviolet curing sealant was cured by irradiating via an ultraviolet lamp. Then, 20 Vp-p of alternating current was applied between the two ITO electrodes, and after 30 J of ultraviolet was irradiated under a driving state of the liquid crystal, the liquid crystal display element of example 1 was obtained. The liquid crystal display element of example 1 was evaluated by each of the following evaluation methods, and the results thereof are as shown in Table 3.

Example 2 to Example 15

The liquid crystal alignment agent, the liquid crystal alignment film, and the liquid crystal display element of each of example 2 to example 15 were respectively prepared by the same steps as example 1, and the difference thereof is: the types and the usage amounts of the components were changed, as shown in Table 3. The liquid crystal display element of each of examples 2 to 15 was evaluated with the evaluation methods below, and the results thereof are as shown in Table 3.

Comparative Example 1 to Comparative Example 13

The liquid crystal alignment agent, the liquid crystal alignment film, and the liquid crystal display element of each of comparative example 1 to comparative example 13 were respectively prepared by the same steps as example 1, and the difference is: the types and the usage amounts of the components were changed, as shown in Table 4. The liquid crystal display element obtained in each of comparative example 1 to comparative example 13 was evaluated with the evaluation methods below, and the results thereof are as shown in Table 4.

The compounds corresponding to the abbreviations in Table 3 and Table 4 are as shown below.

ABBREVIATION COMPONENT

  • A-1-1 Polymer (A-1-1)
  • A-1-2 Polymer (A-1-2)
  • A-1-3 Polymer (A-1-3)
  • A-1-4 Polymer (A-1-4)
  • A-1-5 Polymer (A-1-5)
  • A-2-1 Polymer (A-2-1)
  • A-2-2 Polymer (A-2-2)
  • A-2-3 Polymer (A-2-3)
  • A-2-4 Polymer (A-2-4)
  • A-2-5 Polymer (A-2-5)
  • A-2-6 Polymer (A-2-6)
  • A-2-7 Polymer (A-2-7)
  • A-2-8 Polymer (A-2-8)
  • A-2-9 Polymer (A-2-9)
  • A-2-10 Polymer (A-2-10)
  • B-1 Polysiloxane (B-1)
  • B-2 Polysiloxane (B-2)
  • B-3 Polysiloxane (B-3)
  • B-4 Polysiloxane (B-4)
  • B-5 Polysiloxane (B-5)
  • B-6 Polysiloxane (B-6)
  • B-7 Polysiloxane (B-7)
  • B′-1 Polysiloxane (B′-1)
  • B′-2 Polysiloxane (B′-2)
  • B′-3 Polysiloxane (B′-3)
  • C-1 Polymerizable compound (C-1) containing benzophenone structure
  • C-2 Polymerizable compound (C-2) containing benzophenone structure
  • C-3 Polymerizable compound (C-3) containing benzophenone structure
  • C-4 Polymerizable compound (C-4) containing benzophenone structure
  • C-5 Polymerizable compound (C-5) containing benzophenone structure
  • C-6 Polymerizable compound (C-6) containing benzophenone structure
  • D-1N-methyl-2-pyrrolidone (NMP)
  • D-2 Ethylene glycol n-butyl ether
  • D-3 N,N-dimethylacetamide
  • E-1N,N,N′,N′-tetraepoxypropyl-4,4′-diaminodiphenyl methane
  • E-2 N,N-epoxypropyl-p-glycidoxyaniline

    <Evaluation Methods>

    a. Imidization Ratio

The imidization ratio refers to the proportion of the number of imide rings based on the total amount of the number of amic acid functional groups and the number of imide rings in the polymer, and is represented in percentage.

The detection method includes dissolving the polymers of the synthesis examples in a suitable deuteration solvent (for instance, deuterated dimethyl sulfoxide) after respectively performing drying under reduced pressure. Then, a result of 1H-nuclear magnetic resonance (1H-NMR) was detected under room temperature (such as 25° C.) and using tetramethylsilane as reference material. The imidization ratio (%) was obtained by equation (1).s

Imidizationratio(%)=1-Δ1Δ2α100%equation(1)

    • Δ1: peak area generated due to chemical shift of an NH group proton near 10 ppm;
    • Δ2: peak area of other protons;
    • α: number ratio of one proton of NH group relative to other protons in precursor (polyamic acid) of polymer.

b. Resistance to Ultraviolet Decay

The resistance to ultraviolet decay of the liquid crystal display element was evaluated via the voltage holding ratio of the liquid crystal display element. More specifically, the measuring method of the voltage holding ratio of the liquid crystal display element is as described below.

The voltage holding ratio of the liquid crystal display element of each example and comparative example was respectively measured with an electrical measuring machine (made by Toyo Corporation, Model 6254). The test conditions include the application of a voltage of 4 V for 2 ms, release of the voltage, and measurement of the voltage holding ratio (calculated as V1) 1667 ms from release. Then, after the liquid crystal display element was irradiated with 30 mJ/cm2 of ultraviolet (model of ultraviolet irradiation machine: KN-SH48K1, made by Kuang Neng), the voltage holding ratio (calculated as V2) after ultraviolet irradiation was measured with the same test conditions. Lastly, percentage change of voltage holding ratio (calculated as VUV-decay (%)) was obtained by calculating with equation (2). A lower percentage change of voltage holding ratio indicates better resistance to ultraviolet decay of the liquid crystal display element.

VUV-decay(%)=V1-V2V1100%equation(2)

The evaluation criteria of percentage change of voltage holding ratio are as shown below.

    • ⊚: VUV-decay<3%
    • ◯: 3%≤VUV-decay<5%
    • Δ: 5%≤VUV-decay<10%
    • X: 10%≤VUV-decay

c. Mura Defect

The liquid crystal display element of each of the examples and the comparative examples was observed for the generation of mura defect via a polarizing plate under a backlight source irradiation of a standard C light source. The evaluation criteria of mura defect are as shown below.

    • ⊚: no mura defect.
    • ◯: slight mura defect, but insignificant.
    • Δ: significant mura defect.
    • X: severe mura defect.


TABLE 3
Component
Example
(unit: parts by weight
1
2
3
4
5
6
7
8
Polymer (A)
A-1-1
100
A-1-2
100
A-1-3
100
A-1-4
100
A-1-5
100
A-2-1
100
A-2-2
100
A-2-3
100
A-2-4
A-2-5
A-2-6
A-2-7
A-2-8
A-2-9
A-2-10
Polysiloxane
B-1
5
3
10
(B)
B-2
10
25
B-3
20
B-4
1
B-5
B-6
15
2
B-7
Other
B′-1
3
polysiloxanes
B′-2
(B′)
B′-3
Polymerizable
C-1
8
20
compound (C)
C-2
12
4
10
containing
C-3
5
benzophenone
C-4
20
3
structure
C-5
10
C-6
5
Solvent (D)
D-1
1200
900
250
2300
950
D-2
1200
2000
900
2800
1000
3200
D-3
500
900
2200
1050
Additive (E)
E-1
3
E-2
5
Resistance to
ultraviolet decay
Mura defect
Component
Example
(unit: parts by weight)
9
10
11
12
13
14
15
Polymer (A)
A-1-1
50
A-1-2
A-1-3
A-1-4
A-1-5
A-2-1
A-2-2
A-2-3
A-2-4
100
A-2-5
100
A-2-6
100
A-2-7
100
A-2-8
100
A-2-9
50
A-2-10
100
Polysiloxane
B-1
10
(B)
B-2
12
6
B-3
12
18
B-4
10
B-5
8
B-6
3
B-7
20
Other
B′-1
polysiloxanes
B′-2
(B′)
B′-3
Polymerizable
C-1
12
compound (C)
C-2
12
2
containing
C-3
6
30
benzophenone
C-4
10
structure
C-5
5
C-6
12
20
Solvent (D)
D-1
980
2500
2000
D-2
2700
1500
250
850
D-3
1580
760
900
1950
1800
Additive (E)
E-1
2
E-2
1
Resistance to
ultraviolet decay
Mura defect


TABLE 4
Component
Comparative example
unit: parts by weight
1
2
3
4
5
6
7
Polymer (A)
A-1-1
A-1-2
100
A-1-3
A-1-4
100
A-1-5
100
A-2-1
100
A-2-2
A-2-3
A-2-4
A-2-5
A-2-6
100
A-2-7
A-2-8
A-2-9
A-2-10
Polysiloxane
B-1
100
(B)
B-2
B-3
B-4
B-5
B-6
15
B-7
Other
B′-1
100
polysiloxanes
B′-2
1
(B′)
B′-3
3
Polymerizable
C-1
8
compound (C)
C-2
12
4
containing
C-3
5
benzophenone
C-4
20
10
structure
C-5
C-6
Solvent (D)
D-1
1200
900
250
D-2
1200
900
2000
1000
1500
2800
D-3
900
500
1050
2200
760
Additive (E)
E-1
3
E-2
Resistance to
X
X
X
X
X
X
Δ
ultraviolet decay
Mura defect
X
X
Δ
Δ
Δ
Δ
X
Component
Comparative example
(unit: parts by weight)
8
9
10
11
12
13
Polymer (A)
A-1-1
A-1-2
100
A-1-3
100
A-1-4
A-1-5
A-2-1
A-2-2
A-2-3
A-2-4
A-2-5
A-2-6
A-2-7
100
A-2-8
A-2-9
A-2-10
100
Polysiloxane
B-1
(B)
B-2
6
B-3
100
B-4
B-5
B-6
B-7
Other
B′-1
50
polysiloxanes
B′-2
50
10
(B′)
B′-3
20
Polymerizable
C-1
compound (C)
C-2
containing
C-3
benzophenone
C-4
structure
C-5
C-6
Solvent (D)
D-1
2500
900
900
D-2
900
2000
900
2000
850
D-3
900
900
500
900
500
1800
Additive (E)
E-1
2
E-2
1
Resistance to
Δ
X
X
X
X
X
ultraviolet decay
Mura defect
X
X
X
X
X
X

Comparative Example 14

The liquid crystal alignment agent, the liquid crystal alignment film, and the liquid crystal display element of comparative example 14 were prepared with the same steps as comparative example 11, wherein the types and the usage amounts of the components were substantially the same, and the difference is: 2.4 wt % of the polymerizable compound (C-1) containing a benzophenone structure was further added in the used liquid crystal layer. After the obtained liquid crystal display element was also evaluated via the above evaluation methods, the performances of resistance to ultraviolet decay and mura defect thereof were both X.

<Evaluation Results>

It can be known from Table 3 and Table 4 that, in comparison to the liquid crystal display elements (example 1 to example 15) obtained from the liquid crystal alignment agent containing all of the polymer (A), the polysiloxane (B), and the polymerizable compound (C) containing a benzophenone structure, the liquid crystal display elements of comparative example 1 to comparative example 13 do not have resistance to ultraviolet decay and have the issue of severe mura defect.

Moreover, when the polymer (A) (i.e., polymer (A-2-4) to polymer (A-2-9)) having an imidization ratio of 30% to 90% is used (example 9 to example 14), the resistance to ultraviolet decay of the liquid crystal display element is better.

Moreover, when the polymerizable compound (C) containing a benzophenone structure having two or more photoreactive groups (example 3 to example 5, example 7, example 10 to example 12, and example 14 to example 15) is used, the resistance to ultraviolet decay of the liquid crystal display element is better.

Moreover, when the polysiloxane (B) containing a group containing an epoxy group (i.e., polysiloxane (B-2) to polysiloxane (B-4)) is used (example 2 to example 4, example 8 to example 10, and example 12 to example 14), the issue of mura defect of the liquid crystal display element can be further alleviated.

Moreover, when the polymer (A) contains at least one of the diamine compounds (a2) represented by formula (II-1) and formula (II-2) (example 3 to example 5, example 8 to example 10, and example 15), the issue of mura defect of the liquid crystal display element can be further alleviated.

Moreover, when the polymer (A) contains at least one of the diamine compounds (a2) represented by formula (II-26) and formula (II-30) (example 2, example 5, example 8, and example 12), the resistance to ultraviolet decay of the liquid crystal display element can be further increased.

Moreover, it can be known according to the evaluation results of comparative example 14 that, when the polymerizable compound (C) containing a benzophenone structure is further added in the used liquid crystal layer, the liquid crystal display element does not have resistance to ultraviolet decay and has the issue of severe mura defect.

Based on the above, in the SCVA-type liquid-crystal alignment agent of the invention, in addition to containing a polymer and a solvent, a polymerizable compound containing a benzophenone structure is further added in the liquid crystal alignment agent, and a photopolymerizable compound is not added in the liquid crystal layer as is the case with a polymer-stabilized alignment-type. As a result, the known issue of contamination of the liquid crystal layer from an impurity is solved.

Moreover, the liquid crystal alignment agent of the invention contains a polysiloxane of a specific polymerizable unsaturated group (such as an acryloyloxy group, a methacryloyloxy group, and a carbon-carbon double bond), such that the resistance to ultraviolet decay of the liquid crystal display element is good; moreover, the liquid crystal alignment agent of the invention contains a polymerizable compound containing a benzophenone structure, such that the liquid crystal display element does not have the issue of mura defect. As a result, the liquid crystal alignment agent of the invention is suitable for the fabrication of a liquid crystal alignment film and a liquid crystal display element.

Although the invention has been described with reference to the above embodiments, it will be apparent to one of the ordinary skill in the art that modifications to the described embodiments may be made without departing from the spirit of the invention. Accordingly, the scope of the invention is defined by the attached claims not by the above detailed descriptions.

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21.85/100 Score

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59.0/100 Score

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66.32/100 Score

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47.0/100 Score

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22.06/100 Score

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Citation

Patents Cited in This Cited by
Title Current Assignee Application Date Publication Date
液晶取向剂及液晶显示元件 JSR株式会社 08 October 2002 09 April 2003
液晶配向剂、液晶配向膜、液晶显示元件以及液晶显示元件的制造方法 JSR株式会社 07 March 2013 25 September 2013
光配向用液晶配向剂、液晶配向膜及其制造方法、液晶显示元件、化合物、以及聚合物 JSR株式会社 26 June 2013 15 January 2014
Alignment Film Material and Corresponding Liquid Crystal Panel SHENZHEN CHINA STAR OPTOELECTRONICS TECHNOLOGY CO., LTD. 31 January 2013 31 July 2014
液晶显示装置及其制造方法 夏普株式会社 28 April 2010 28 November 2012
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