LIQUID CRYSTAL ALIGNING AGENT, FILM, DEVICE HAVING THE SAME, AND METHOD FOR PRODUCING THE SAME

Abstract

The present application relates to a liquid crystal aligning agent, a liquid crystal alignment film and a method for producing the same, as well as a liquid crystal display device. The liquid crystal aligning agent comprises (i) a first polyamic acid having a photoreactive group without a liquid crystal group; (ii) a second polyamic acid having a liquid crystal group without a photoreactive group; (iii) a third polyamic acid having both a liquid crystal group and a photoreactive group; (iv) a fourth polyamic acid having neither a photoreactive group nor a liquid crystal group. The liquid crystal display device using the liquid crystal alignment film formed by the liquid crystal aligning agent provided by the present disclosure has a high display contrast and an improved AC residual image.

Claims

1. A liquid crystal aligning agent, comprising: (i) a first polyamic acid having a photoreactive group without a liquid crystal group; (ii) a second polyamic acid having a liquid crystal group without a photoreactive group; (iii) a third polyamic acid having both a liquid crystal group and a photoreactive group; and (iv) a fourth polyamic acid having neither a photoreactive group nor a liquid crystal group.

2. The liquid crystal aligning agent claimed in claim 1, the first polyamic acid has the structure of Formula (II) ##STR00041## wherein R.sub.1 and R.sub.2 each independently is selected from the group consisting of photoreactive group, an alkyl group, or a combination of at least two selected; wherein at least one of R.sub.1 and R.sub.2 comprises the photoreactive group; wherein the alkyl groups are selected from the group consisting of substituted or unsubstituted linear or branched alkylene groups of C1-C10, substituted or unsubstituted linear or branched alkenylene groups of C2-C10 and substituted or unsubstituted linear or branched alkynylene of C2-C10, and a combination of at least two selected therefrom; and wherein the photoreactive groups are selected from the group consisting of isomeric photoreaction groups, bridging photoreaction groups, fries transferable photoreaction groups and decomposable photoreactive groups.

3. The liquid crystal aligning agent claimed in claim 1, wherein the second polyamic acid having a liquid crystal group without the photoreactive group has the structure of Formula (II), ##STR00042## wherein R.sub.3 and R.sub.4 each independently is selected from the group consisting of liquid crystal groups and alkyl groups, and a combination of at least two selected therefrom; wherein the alkyl groups are selected from the group consisting of substituted or unsubstituted linear or branched alkylene groups of C1-C10, substituted or unsubstituted linear or branched alkenylene groups of C2-C10 and substituted or unsubstituted linear or branched alkynylene of C2-C10, and a combination of at least two selected therefrom; wherein the liquid crystal groups are selected from the group consisting of substituted or unsubstituted phenyl of C6-C20, substituted or unsubstituted biphenyl of C12-050, substituted or unsubstituted heterocyclic group of C2-C20, and substituted or unsubstituted phenylpropyl of C9-C50; and wherein n.sub.2 is an integer ≧1.

4. The liquid crystal aligning agent in claim 1, wherein the third polyamic acid having both the liquid crystal group and the photoreactive group has the structure of Formula (III), ##STR00043## wherein R.sub.5, R.sub.6 and R.sub.7 each independently is selected from the group consisting of alkyl groups, liquid crystal groups and photoreactive groups, and a combination of at least two selected therefrom; wherein at least one of R.sub.5, R.sub.6 and R.sub.7 is the liquid crystal group, and at least one of them is the photoreactive group; wherein the alkyl group is selected from the group consisting of substituted or unsubstituted linear or branched alkylene groups of C1-C10, substituted or unsubstituted linear or branched alkenylene groups of C2-C10, and substituted or unsubstituted linear or branched alkynylene of C2-C10, and a combination of at least two selected therefrom; wherein the liquid crystal group are selected from the group consisting of substituted or unsubstituted phenyl of C6-C20, substituted or unsubstituted biphenyl of C12-050, substituted or unsubstituted heterocyclic group of C2-C20, and substituted or unsubstituted phenylpropyl of C9-C50; and wherein the photoreactive groups are selected from the group consisting of isomeric photoreaction groups, bridging photoreaction groups, fries transferable photoreaction groups and decomposable photoreactive groups.

5. The liquid crystal aligning agent in claim 1, wherein the fourth polyamic acid having neither the liquid crystal group nor the photoreactive group has the structure of Formula (IV), ##STR00044## wherein R.sub.8 and R.sub.9 each independently is selected from the group consisting of alkyl groups, and a combination of at least two selected therefrom; wherein the alkyl groups are selected from the group consisting of substituted or unsubstituted linear or branched alkylene groups of C1-C10, substituted or unsubstituted linear or branched alkenylene groups of C2-C10, and substituted or unsubstituted linear or branched alkynylene of C2-C10; and n.sub.4 is an integer 1.

6. A liquid crystal alignment film in claim 1, wherein the liquid crystal alignment film is prepared from the liquid crystalline aligning agent.

7. The liquid crystal alignment film claimed in claim 6, wherein the upper layer of the liquid crystal alignment film comprises the first polyamic acid having a photoreactive group without the liquid crystal group, or the third polyamic acid having both the liquid crystal group and the photoreactive group; and wherein the lower layer of the liquid crystal alignment film comprises the second polyamic acid having a liquid crystal group without the photoreactive group, or the fourth polyamic acid having neither photoreactive group nor the liquid crystal group.

8. A method for producing the liquid crystal alignment film in claim 6, comprising the following steps, (a) applying a liquid crystal aligning agent on a substrate to form a coating film; (b) pre-baking the substrate; and (c) performing light alignment to the coating film obtained in step (a), followed by post-baking to form a liquid crystal alignment film.

9. A liquid crystal display device, comprising the liquid crystal alignment film in claim 6.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0022] FIG. 1 shows the schematic structure of the light alignment film in the prior art.

[0023] FIG. 2 shows the schematic structure of the light alignment film in the present disclosure.

[0024] FIG. 3a shows the internal topical structure diagram of the liquid crystal display device present by the present disclosure.

[0025] FIG. 3b shows the overall structure diagram of the liquid crystal display device present by the present disclosure.

DETAIL DESCRIPTION

[0026] In order to better understand the present disclosure, the present disclosure lists the following examples. Those skilled in the art shall know that the embodiments are merely illustrative of the disclosure and shall not be construed as limiting the present disclosure.

[0027] In one specific embodiment, the present disclosure provides a liquid crystal aligning agent comprising the following components, [0028] (i) a polyamic acid having a photoreactive group without a liquid crystal group; [0029] (ii) a polyamic acid having a liquid crystal group without a photoreactive group; [0030] (iii) a polyamic acid having both a liquid crystal group and a photoreactive group; and [0031] (iv) a polyamic acid having neither a photoreactive group nor a liquid crystal group.

[0032] The polyamic acid of the present disclosure has the structure of Formula (J-1) and can be obtained by reacting tetracarboxylic dianhydride with diamine:

##STR00001##

[0033] Said “polymerizable prepolymer capable of reacting with a polyamic acid to form a PI film” is exemplarily selected from the group consisting of polymers, such as polyamic acid, polyimide, polyamide ester as shown in Formula (J-1), or a combination of at least two selected therefrom.

[0034] Said “polymerizable monomer capable of reacting with a polyamic acid to form a PI film” can exemplarily be selected from the group consisting of tetracarboxylic dianhydride and diamine, wherein said tetracarboxylic dianhydride has the structure of Formula (J-2); said diamine has the structure of Formula (J-3)

##STR00002##

[0035] In the structures of formulas (J-1), (J-2) and (J-3), the structural units of A and B may be selected according to the design of the PI film. For example, the photoreactive group in (i) polyamic acid having a photoreactive group without a liquid crystal group may be at the position of A or B. As for (ii) polyamic acid having a liquid crystal group without a photoreactive group of the present application, the liquid crystal group therein may be at the position of A or B. As for (iii) polyamic acid having both a liquid crystal group and a photoreactive group, the liquid crystal group and photoreactive group therein may be independently at the position of A or B.

[0036] As for the component (iv) polyamic acid having neither photoreactive group nor liquid crystal group, the present application makes no specific definition to the selection of the structural units of A or B, and they may be any known groups in the art.

[0037] The typical but non-limitative example of the component (iv) may be polyamic acid obtained by reacting tetracarboxylic dianhydride with diamine.

[0038] The typical but non-limitative examples of tetracarboxylic dianhydride are selected from the group consisting of aliphatic tetracarboxylic dianhydrides, alicyclic tetracarboxylic dianhydrides, aromatic tetracarboxylic dianhydrides and the like. The exemplary aliphatic tetracarboxylic dianhydrides may include 1,2,3,4-butanetetracarboxylic dianhydride and the like. The exemplary alicyclic tetracarboxylic dianhydrides are selected from the group consisting of 1,2,3,4-cyclobutanetetracarboxylic dianhydride, 2,3,5-tricarboxylcyclopentyl acetic acid dianhydride, 1,3,3a,4,5,9b-hexahydro-5-(tetrahydro-2,5-dioxo-3-furyl)-naphtho [1,2-c]furan-1,3-dione, 1,3,3a,4,5,9b-hexahydro-8-methyl-5-(tetrahydro-2,5-dioxo-3-furyl) naphtho-[1,2-c]furan-1,3-dione, 3-oxabicyclo[3.2.1]octane-2,4-dione-6-spiro-3′-(tetrahydrofuran-2′,5′-dione), 5-(2,5-dioxotetrahydro-3-furan)-3-methyl-3-cyclohexene-1,2-dicarboxylic anhydride, 3,5,6-tricarboxy-2-carboxy-methyl norbomane-2:3, 5:6-dianhydride, 4,9-dioxatricyclo [5.3.1.0.sup.2,6]undecane-3,5,8,10-tetraone, and cyclohexane tetracarboxylic dianhydride. The exemplary aromatic tetracarboxylic dianhydride may include pyromellitic dianhydride and the like.

[0039] The typical but non-limitative examples of diamines are selected from the group comprising aliphatic diamines, alicyclic diamines, aromatic diamines or diamino organosiloxanes and the like.

[0040] The typical but non-limitative examples of aliphatic diamines are selected from the group consisting of ethylenediamine, 1,3-propanediamine, butanediamine, 2,5-dimethylhexamethylene diamine, m-xylylenediamine, tetramethylene diamine, pentamethylene diamine, hexamethylene diamine diamine and the like. The typical but non-limitative examples of alicyclic diamines are selected from the group consisting of 1,2-cyclobutanediamine

##STR00003##

1,3-cyclopentylenediamine

##STR00004##

1,3-bis(aminomethyl) cyclohexane and the like.

[0041] The typical but non-limitative examples of aromatic diamines include the compound having the structure of Formula (J-4)

##STR00005##

[0042] wherein X.sub.1 and X.sub.2 are each independently selected from the group consisting of fluorine atom, iodine atom, chlorine atom, hydroxyl group, C1-C10 hydroxyalkyl group, carboxyl group, ester group, C1-C10 substituted or unsubstituted alkyl group, C2-C12 substituted or unsubstituted alkenyl group, C3-C13 substituted or unsubstituted alkynyl group and C6-C20 aromatic groups, optionally methyl, ethyl, alkoxy, monofluoro-substituted methyl, monofluoro-substituted ethyl, benzyl, phenethyl, alkoxy-substituted benzoate group

##STR00006##

wherein R.sub.30, R.sub.31 and R.sub.32 are selected from the group consisting of alkyl groups containing at least one carbon atom, which may be C1-C20 alkyl group, or alkyl groups having more carbon atoms) and acrylate methylene group

##STR00007##

[0043] The typical but non-limitative examples of aromatic diamines are selected from the group consisting of p-phenylenediamine, 4,4′-diaminodiphenyl sulfide, 1,5-diaminonaphthalene, 2,2′-dimethyl-4,4′-diaminobiphenyl, 2,2′-bis(trifluoro-methyl)-4,4′-diaminobiphenyl, 2,7-diaminofluorene, 4,4′-diaminodiphenyl ether, 1,5-diaminonaphthalene, 2,2′-dimethyl-4,4′-diaminobiphenyl, 2,2′-bis(trifluoro-methyl)-4,4′-diaminobiphenyl, 2,7-diaminofluorene, 4,4′-diminodiphenyl ether, 2,2- bis[4-(4-aminophenoxy)phenyl] propane, 9,9-bis(4-aminophenyl)fluorene, 2,2-bis[4-(4-aminophenoxy)phenyl] hexafluoropropane, 2,2-bis(4-aminophenyl)-hexafluoropropane, 4,4′-(p-phenylene diisopropylidene), 4,4′-(m-phenylene-diisopropylidene)diphenylamine, 1,4-bis(4-aminophenoxy)benzene, 4,4′-bis(4-amino-phenoxy)biphenyl, 2,6-diaminopyridine, 3,4-diaminopyridine, 2,4-diaminopyrimidine, 3,6-diaminoacridine, 3,6-diaminocarbazole, N-methyl-3,6-diaminocarbazole, N-ethyl-3,6-diaminocarbazole, N-phenyl-3,6-diaminocarbazole, N,N′-bis (4-aminophenyl)-benzidine N,N′-bis(4-aminophenyl)-N,N′-dimethylbenzidine, 1,4-bis-(4-aminophenyl)piperazine, 1-(4-aminophenyl)-2, 3-dihydro-1,3,3-trimethyl-1H-inden-5-amine, 1-(4-aminophenyl)-2,3-dihydro-1,3,3-trimethyl-1H-inden-6-amine, 4-(4′-trifluoromethoxybenzoyloxy)cyclohexyl-3,5-diaminobenzoate, 4-(4′-trifluoromethylbenzoyloxy)cyclohexyl-3,5 -diaminobenzoate, 1,1-bis (4-((amino-phenyl)methyl)phenyl)-4-butylcyclohexane, 1,1-bis(4-((aminophenyl)methyl) phenyl)-4-heptyl-cyclohexane, 1,1-bis(4-((aminophenoxy)methyl)phenyl)-4-heptyl-cyclohexane, 1,1-bis (4-((aminophenyl)methyl)phenyl)-4-(4-heptylcyclohexyl)-cyclohexane, 4-aminobenzylamine, 3-aminobenzylamine and the like.

[0044] The exemplary diamino organosiloxanes include 1,3-bis(3-aminopropyl)tetra-methyldisiloxane and the like.

[0045] In the components of the liquid crystal aligning agent of the present disclosure, the photoreactive groups (exemplarily may include isomeric photoreaction groups, bridging type photoreactive groups, fries transferable photoreaction groups and decomposable photoreactive groups) may be linked in a branched form at the position A or the position B of the molecular chain of the polyamic acid (J-1). The exemplary connection mode is shown in Formula (J-5) (In Formula (J-5), the photoreactive group linked in the branched form is represented by FG.sub.1), or is linked to the position A or the position B of the polyamic acid (J-1) molecular chain in the form of a block. The exemplary connection mode is shown in Formula (J-6) (In Formula (J-6), the photoreactive group linked in the block form is represented by FG.sub.2)

##STR00008##

wherein FG.sub.1 represents a decomposable photoreactive group linked in a branched form; FG.sub.2 represents a decomposable photoreactive group linked in a block form; X.sub.3 represents any group selected from the group consisting of, e.g. hydrogen atom, fluorine atom, iodine atom, chlorine atom, hydroxyl group, C1 to C10 hydroxyalkyl groups, carboxyl groups, ester groups, C1 to C10 substituted or unsubstituted alkyl groups, C2 to C12 substituted or unsubstituted alkenyl groups, C3 to C13 substituted or unsubstituted alkynyl groups, C6 to C20 aromatic groups, optionally methyl, ethyl, alkoxy, monofluoro-substituted methyl, monofluoro-substituted ethyl, benzyl, phenethyl, alkoxy-substituted benzoate

##STR00009##

wherein R.sub.30, R.sub.31 and R.sub.32 are selected from the group consisting of alkyl groups containing at least one carbon atom, e.g. C1-C20 alkyl groups, or alkyl groups having more carbon atoms), acrylate methylene

##STR00010##

optionally methyl; f is an integer which is greater than 1, e.g. 2, 3, 4, 5, 6, 11, 15, 23 and the like; X.sub.4 and X.sub.5 represent empty bonds, or any group having two bonds, e.g. oxygen atom, sulfur atom, C1-C10 substituted or unsubstituted alkylene group, C2-C12 substituted or unsubstituted alkenylene group, C3-C13 substituted or unsubstituted alkynylene group, C6-C20 arylene, optionally methylene, ethylene, alkyleneoxy, monofluoro-substituted methylene, monofluoro-substituted ethylene, benzylidene, phenylethylene and the like.

[0046] The photoreactive groups are selected from the group consisting of isomeric photoreaction groups, bridging photoreaction groups, fries transferable photoreaction groups and decomposable photoreactive groups.

[0047] The exemplary isomeric photoreaction groups include the molecules containing azo bonds, and the isomeric photoreaction groups linked in the branched form optionally are selected from any or a combination of at least two of

##STR00011##

the isomeric photoreaction groups linked in the block form optionally are selected from any or a combination of at least two of

##STR00012##

wherein R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5, R.sub.6, R.sub.7, R.sub.8, R.sub.9, R.sub.11, R.sub.12, R.sub.13, R.sub.14, R.sub.15, R.sub.16, R.sub.17, R.sub.18 and R.sub.19 are each independently selected from hydrogen atom, fluorine atom, iodine atom, chlorine atom, hydroxyl group, C1-C10 hydroxyalkyl group, carboxyl group, ester group, C1-C10 substituted or unsubstituted alkyl group, C2-C12 substituted or unsubstituted alkenyl group, C3-C13 substituted or unsubstituted alkynyl group and C6-C20 aromatic groups.

[0048] The isomeric photoreaction groups linked in the block form are optionally

##STR00013##

[0049] The decomposable photoreactive groups linked in the branched form include any or a combination of at least two of

##STR00014##

the decomposable photoreactive groups linked in the block form include any or a combination of at least two of

##STR00015##

wherein R.sub.20 is selected from the group consisting of hydrogen atom, C1-C10 hydroxyalkyl group, carboxyl group, ester group, C1-C10 substituted or unsubstituted alkyl group, C2-C12 substituted or unsubstituted alkenyl group, C3-C13 substituted or unsubstituted alkynyl group and C6-C20 aromatic groups.

[0050] The exemplary bridging photoreaction groups may have the structure of

##STR00016##

wherein the bridging photoreaction groups are linked to the position A or B of the molecular chain of polyamic acid (J-1) via R.sub.1′ and R.sub.2′, wherein R.sub.1′, R.sub.2′, R.sub.3′ and R.sub.4′ are each independently selected from hydrogen atom, fluorine atom, iodine atom, chlorine atom, hydroxyl group, C1-C10 hydroxyalkyl group, carboxyl group, ester group, C1-C10 substituted or unsubstituted alkyl group, C2-C12 substituted or unsubstituted alkenyl group, C3-C13 substituted or unsubstituted alkynyl group, C6-C20 aromatic groups and C6-C20 arylene groups.

[0051] The exemplary fries transferable photoreaction groups may have the structure of

##STR00017##

wherein R.sub.5′ and R.sub.6′ are each independently selected from hydrogen atom, fluorine atom, iodine atom, chlorine atom, hydroxyl group, C1-C10 hydroxyalkyl group, carboxyl group, ester group, C1-C10 substituted or unsubstituted alkyl group, C2-C12 substituted or unsubstituted alkenyl group, C3-C13 substituted or unsubstituted alkynyl group, C6-C20 aromatic groups and C6-C20 arylene groups.

[0052] In the components of the liquid crystal aligning agent of the present disclosure, the mesogen group may be linked in the form of a block at the position A or B of the molecular chain of the polyamic acid (J-1) (J-7), and the exemplary linking mode is shown in Formula (J-7) (wherein, for convenience, GG is used to represent the mesogen group linked in the block form for convenience of illustration).

—X.sub.6—GG—X.sub.7   Formula (J-7)

[0053] In Formula (J-7), X.sub.6 and X.sub.7 represent empty bonds, or any group having two bonds, e.g. oxygen atom, sulfur atom, C1-C10 substituted or unsubstituted alkylene group, C2-C12 substituted or unsubstituted alkenylene group, C3-C13 substituted or unsubstituted alkynylene group, C6-C20 aromatic groups and C6-C20 arylene groups, optionally methylene, ethylene, alkyleneoxy, monofluoro-substituted methylene, monofluoro-substituted ethylene, benzylidene, phenylethylene and the like.

[0054] In the present disclosure, the liquid crystal group means that the inside of the main chain cannot be internally rotated, or, although the internal rotation does not change the direction of the chain, mainly referring to a cyclic structures such as benzene ring.

[0055] In the aforesaid embodiment, the liquid crystal group optionally comprises any one or a combination of at least two of the following structures: polybenzothienyl, poly-3,4-ethylenedioxythienyl, polypyrrolyl, biphenyl group,

##STR00018##

wherein R.sub.21, R.sub.22, R.sub.23, R.sub.24, R.sub.25, R.sub.26, R.sub.27 and R.sub.28 are each independently selected from the group consisting of hydrogen atom, C1-C3 substituted or unsubstituted alkoxy group, amino group and dialkylamino group, optionally biphenyl, terphenyl and the like.

[0056] The examples of the liquid crystal groups described above do not show any connectors except for Structures A and B in the polyamic acid shown in Formula (J-1), and those skilled in the art can link these groups according to their professional knowledge. The present disclosure illustratively provides the following examples, which are not to be taken as a specific limitation of the present disclosure.

[0057] For the liquid crystal group capable of being used as Structure A, their linking modes thereof are shown as follows

##STR00019## ##STR00020##

[0058] For the liquid crystal group capable of being used as Structure B, their linking modes thereof are shown as follows

##STR00021##

[0059] In one preferred embodiment, said (i) polyamic acid having a photoreactive group and no liquid crystal group has the structure of Formula (I)

##STR00022##

wherein R.sub.1 and R.sub.2 each independently are selected from the group consisting of photoreactive groups and alkyl groups, or a combination of at least two selected therefrom; at least one of R1 and R2 is a photoreactive group;
the alkyl groups are selected from the group consisting of substituted or unsubstituted linear or branched alkylene groups of C1-C10, substituted or unsubstituted linear or branched alkenylene groups of C2-C10 and substituted or unsubstituted linear or branched alkynylene of C2-C10, or a combination of at least two selected therefrom;
the photoreactive groups are selected from the group consisting of isomeric photoreaction groups, bridging photoreaction groups, fries transferable photoreaction groups and decomposable photoreactive groups.

[0060] In one exemplary embodiment, the isomeric photoreaction group comprises any one of or a combination of at least two selected from the following structure,

##STR00023##

wherein R.sub.11, R.sub.12, R.sub.13, R.sub.14, R.sub.15, R.sub.16, R.sub.17, R.sub.18, R.sub.19, R.sub.20, R.sub.21, R.sub.22, R.sub.23, R.sub.24 and R.sub.25 are each independently selected from the group consisting of hydrogen atom, fluorine atom, iodine atom, chlorine atom, hydroxyl group, C1-C10 hydroxyalkyl group, carboxyl group, ester group, C1-C10 substituted or unsubstituted alkyl group, C2-C12 substituted or unsubstituted alkenyl group, C3-C13 substituted or unsubstituted alkynyl group and C6-C20 aromatic groups;
n.sub.1 is an integer of ≧1.

[0061] The exemplary isomeric photoreactive group is attached to the backbone of the polyamic acid of Component (i) by the formula (J-6).

[0062] In one exemplary embodiment, said (ii) polyamic acid having a liquid crystal group without a photoreactive group has the structure of Formula (II)

##STR00024##

wherein R.sub.3 and R.sub.4 each independently are selected from the group consisting of liquid crystal groups and alkyl groups, or a combination of at least two selected therefrom;
the alkyl groups are selected from the group consisting of substituted or unsubstituted linear or branched alkylene groups of C1-C10, substituted or unsubstituted linear or branched alkenylene groups of C2-C10 and substituted or unsubstituted linear or branched alkynylene of C2-C10, or a combination of at least two selected therefrom;
the liquid crystal groups are selected from the group consisting of substituted or unsubstituted phenyl of C6-C20, substituted or unsubstituted biphenyl of C12-050, substituted or unsubstituted heterocyclic group of C2-C20, substituted or unsubstituted phenylpropyl of C9-050;
n.sub.2 is an integer ≧1.

[0063] In one exemplary embodiment, said (iii) polyamic acid having both a liquid crystal group and a photoreactive group has the structure of Formula (III)

##STR00025##

wherein R.sub.5, R.sub.6 and R.sub.7 each independently are selected from the group consisting of alkyl groups, liquid crystal groups and photoreactive groups, or a combination of at least two selected therefrom; at least one of R.sub.5, R.sub.6 and R.sub.7 is a liquid crystal group, and at least one of them is a photoreactive group;
the alkyl groups are selected from the group consisting of substituted or unsubstituted linear or branched alkylene groups of C1-C10, substituted or unsubstituted linear or branched alkenylene groups of C2-C10 and substituted or unsubstituted linear or branched alkynylene of C2-C10, or a combination of at least two selected therefrom;
the liquid crystal groups are selected from the group consisting of substituted or unsubstituted phenyl of C6-C20, substituted or unsubstituted biphenyl of C12-050, substituted or unsubstituted heterocyclic group of C2-C20, substituted or unsubstituted phenylpropyl of C9-050;
the photoreactive groups are selected from the group consisting of isomeric photoreaction groups, bridging photoreaction groups, fries transferable photoreaction groups and decomposable photoreactive groups.

[0064] In one exemplary embodiment, the isomeric photoreaction group comprises any one of or a combination of at least two selected from the following structure,

##STR00026##

wherein R.sub.11, R.sub.12, R.sub.13, R.sub.14, R.sub.15, R.sub.16, R.sub.17, R.sub.18, R.sub.19, R.sub.20, R.sub.21, R.sub.22, R.sub.23, R.sub.24 and R.sub.25 are each independently selected from the group consisting of hydrogen atom, fluorine atom, iodine atom, chlorine atom, hydroxyl group, C1-C10 hydroxyalkyl group, carboxyl group, ester group, C1-C10 substituted or unsubstituted alkyl group, C2-C12 substituted or unsubstituted alkenyl group, C3-C13 substituted or unsubstituted alkynyl group and C6-C20 aromatic groups;
n.sub.1 is an integer ≧1.

[0065] The exemplary isomeric photoreactive group is attached to the backbone of the polyamic acid of Component (iii) by the formula (J-6).

[0066] In one exemplary embodiment, said (iv) polyamic acid having neither a liquid crystal group nor a photoreactive group has the structure of Formula (IV)

##STR00027##

wherein R.sub.8 and R.sub.9 each independently are selected from the group consisting of alkyl groups, or a combination of at least two selected therefrom;
the alkyl groups are selected from the group consisting of substituted or unsubstituted linear or branched alkylene groups of C1-C10, substituted or unsubstituted linear or branched alkenylene groups of C2-C10 and substituted or unsubstituted linear or branched alkynylene of C2-C10;

[0067] n.sub.4 is an integer ≧1.

[0068] In one optional embodiment of the present disclosure, the liquid crystal aligning agent comprises the following components.

[0069] (i) a polyamic acid having a photoreactive group without a liquid crystal group has the structure

##STR00028##

wherein n.sub.1 is 5-20;

[0070] (ii) a polyamic acid having a liquid crystal group without a photoreactive group has the structure of

##STR00029##

wherein n.sub.2 and n.sub.3 are independently 5-20;

[0071] (iii) a polyamic acid having both a liquid crystal group and a photoreactive group has the structure of

##STR00030##

wherein n.sub.4 is independently 5-20;

[0072] (iv) a polyamic acid having neither a photoreactive group nor a liquid crystal group has the structure of

##STR00031##

wherein n.sub.5 is independently 5-20.

[0073] In the liquid crystal aligning agent of the present disclosure, the content of each component may be, for example, [0074] the sum of the contents of the component (i) and (iii) being 30 to 50% by weight, the sum of the contents of the component (ii) and (iv) being 50 to 70% by weight; the ratio of the addition ratio of the component (iii) may be 1:1, the ratio of the component (ii) to the component (iv) may be 1:1; the sum of the contents of the components (i), (ii), (iii) and (iv) is 100% by weight.

[0075] In order to facilitate the operation of the alignment process, the liquid crystal aligning agent of the present disclosure is further provided with a solvent which dissolves the components in the liquid crystal aligning agent. The present disclosure does not specifically limit the type of the solvent. The typical but non-limitative example is selected from γ-BL, NMP and BC, or a combination of at least two selected therefrom, optionally a mixed solvent of 50% γ-BL (γ-butyrolactone), 20% NMP (N-methyl-2-pyrrolidone) and 30% BC (butyl carbonate).

[0076] When the liquid crystal aligning agent is added with the solvent, the liquid crystal aligning agent has a solid content of 5.5 to 6.0 wt. %. Optionally the sum of the mass percentages of the components (i), (ii), (iii) and (iv) is 5.5 to 6.0 wt. %.

[0077] The synthesis of the polyamic acid (including the components (i), (ii), (iii) and (iv)) according to the present disclosure is the technical means which can be obtained by those skilled in the art. The typical but non-limitative synthesis method of polyamic acid comprises [0078] mixing tetracarboxylic dianhydride (having the same structure A as the target polyamic acid) with diamine (having the same structure B as the target polyamic acid) in an organic solvent in a mixing ratio that 0.2 to 2 equivalents of tetracarboxylic dianhydride is added into 1 equivalent of diamine, optionally 0.3 to 1.2 equivalents (acid anhydride equivalent), reacting for 0.1-24 h at 0-100° C.

[0079] The liquid crystal aligning agent according to the present disclosure may further include other functional components capable of improving the stability, electrical properties, and coating film properties of the liquid crystal aligning agent in different levels.

[0080] The present disclosure discloses adding into the PI material a component having a liquid crystal structure, making the polyamic acid dispersed in the upper light aligning layer and having a mesogen structure having one-axis aligning force through which the one-axis alignment of the aforesaid light aligning part can be enhanced. Meanwhile, a liquid crystal structure is also added to the lower conductive layer which also makes contribution to the alignment.

[0081] In one embodiment, the present disclosure further provides a liquid crystal alignment film prepared from the aforesaid liquid crystalline aligning agent.

[0082] In one preferred embodiment, the upper layer (201) of the liquid crystal alignment film comprises (i) polyamic acid 206 having a photoreactive group without a liquid crystal group, and (iii) polyamic acid 203 having both a liquid crystal group and a photoreactive group;

[0083] the lower layer (202) of the liquid crystal alignment film comprises (ii) polyamic acid 205 having a liquid crystal group without a photoreactive group; and (iv) polyamic acid 204 having neither a photoreactive group nor a liquid crystal group.

[0084] The light alignment film obtained by the present disclosure has the schematic structure as shown in FIG. 2. The polyamic acid represented by the solid line has the alignment, i.e. having a photoreactive group; the polyamic acid represented by the dotted line does not have a photoreaction group; the polyamic acid represented by a straight line has a liquid crystal structure; the polyamic acid represented by a curve does not have a liquid crystal structure.

[0085] In FIG. 2, the upper 201 and lower layers 202 of the liquid crystal alignment film are only different from each other. In the preparation of the liquid crystal alignment film, the components of the liquid crystal aligning agents are the spontaneous layers, so that the upper and lower layers cannot be strictly distinguishable by the components. That is to say that the upper polyamic acid is predominantly component (i) 206 and (iii) 203, and may also contain a minor amount of component (ii) 205 and (iv) 204, while the lower polyamic acid is predominantly component (ii) 205 and (iv) 204, and may also contain a minor amount of component (i) 206 and (iii) 203. In addition, it should be noted that the number of various lines shown in FIG. 2 is merely used to illustratively indicate the possible spatial position of each component, and does not represent any component ratio.

[0086] In one embodiment, the present disclosure further provides a method for producing the liquid crystal alignment film, characterized in comprising the following steps, [0087] (a) applying the above liquid crystal aligning agent on a substrate to form a coating film; [0088] (b) pre-baking the substrate on which the coating film is formed; and [0089] (c) performing light alignment to the film obtained in step (b), followed by post-baking to form a liquid crystal alignment film.

EXAMPLES

Example 1

[0090] A liquid crystal aligning agent, characterizing in comprising the following components,

[0091] (i) a polyamic acid having a photoreactive group without a liquid crystal group, the polyamic acid has the structure

##STR00032##

wherein the average value of n.sub.1 was 10.5, and the addition amount was 1 part by weight;

[0092] (ii) a polyamic acid having a liquid crystal group without a photoreactive group, the polyamic acid has the structure:

##STR00033##

wherein the average value of n.sub.2 was 5, and the addition amount was 1 part by weight;

[0093] (iii) a polyamic acid having both a liquid crystal group and a photoreactive group, the polyamic acid has the structure,

##STR00034##

wherein the average value of n.sub.4 was 6.5, and the addition amount was 3 parts by weight;

[0094] (iv) a polyamic acid having neither a photoreactive group nor a liquid crystal group, the polyamic acid has the structure

##STR00035##

wherein the average value of n.sub.5 was 12, and the addition amount was 1 part by weight;

[0095] (v) the solvent being a mixed solvent of γ-BL 50%, NMP 20% and BC 30%, and being added in an amount of 94 parts by weight;

[0096] A liquid crystal alignment film prepared from the liquid crystal aligning agent in Example 1, by the following steps

[0097] (a) applying a liquid crystal aligning agent in Example 1 on a substrate to form a coating film having a certain viscosity and a better diffusion;

[0098] (b) pre-baking at 110° C. for 90 s the substrate on which the coating film is formed;

[0099] (c) irradiating the film obtained in step (b) with linearly polarized light of 254 to 365 nm, and the amount of the bulk being 3000 mJ, to carry out the reaction so as to form an alignment;

[0100] (d) post-baking the substrate processed in step (c) at 230° C. for 30 min to form a liquid crystal alignment film having a thickness of 100±10 nm.

Example 2

[0101] It was different from Example 1 only in that the component (ii) was

##STR00036##

wherein the average value of n.sub.3 was 4.

Example 3

[0102] It was different from Example 1 only in that the component (ii) was added in an amount of 0.5 part by weight, while the component (iv) was added in an amount of 1.5 parts by weight.

Comparison Example 1

[0103] It was different from Example 1 only in comprising no component (ii). As for other components, the component (i) was added in an amount of 1 part by weight; the component (iii) was added in an amount of 3 parts by weight; the component (iv) was added in an amount of 2 parts by weight.

Performance Test

[0104] Contrast test: using CS2000 or CA310 and other machines to measure the contrast of LCD screen, respectively measuring the brightness of the LCD screen displaying the white screen and the black screen, the contrast being defined as bright state brightness/black brightness;

Residual Image Test:

[0105] Lighting the LCD screen in the checkerboard screen for 2 h, and then switching to the 128/255 gray scale screen; determining: After switching to the 128/255 gray scale screen, the checkerboard screen residual does not appear on the LCD screen; the residual image level being defined as A, qualified; when maintaining the 128/255 gray scale screen for 10 s, the checkerboard screen residual disappearing from the LCD screen, the residual image level being defined as B, unqualified; when maintaining the 128/255 gray scale screen for 60 s, the checkerboard screen residual disappearing from the LCD screen, the residual image level being defined as C, which is seriously unqualified.

[0106] The performance test results are shown in Table 1 below.

TABLE-US-00001 TABLE 1 Disappearing time for Black state Residual Residual brightness image image (cd/cm.sup.2) Contrast (S) level Example 1 0.28 1800 0 A Example 2 0.30 1680 0 A Example 3 0.32 1575 9 B Example 1 0.36 1400 45 C

[0107] As can be seen from Table 1, the contrast and the residual image levels of Examples 1 and 2 were greatly improved with respect to Comparison Example 1. Although Example 3 did not meet the residual image specifications as compared to Comparison Example 1, it still made improvement. Therefore, it is presumed that the addition of a liquid crystal group to the lower component of the liquid crystal alignment film can improve the contrast of the liquid crystal display and the residual image level.

Example 4

[0108] A liquid crystal aligning agent, characterizing in comprising the following components,

[0109] (i) a polyamic acid having a photoreactive group and having no liquid crystal group having the structure

##STR00037##

wherein the average value of n.sub.1 was 13, and the addition amount was 1 part by weight;

[0110] (ii) a polyamide acid having a liquid crystal group without a photoreactive group having the structure:

##STR00038##

wherein the average value of n.sub.2 was 5, and the addition amount was 1 part by weight;

[0111] (iii) a polyamide acid having both a liquid crystal group and a photoreactive group having the structure:

##STR00039##

wherein the average value of n.sub.4 was 8.5, and the addition amount was 3 parts by weight;

[0112] (iv) a polyamide acid having neither a photoreactive group nor a liquid crystal group having the structure

##STR00040##

wherein the average value of n.sub.5 was 12, and the addition amount was 1 part by weight;

[0113] (v) the solvent being a mixed solvent of γ-BL 50%, NMP 20% and BC 30%, and being added in an amount of 94 parts by weight;

[0114] A liquid crystal alignment film prepared from the liquid crystal aligning agent in Example 1, by the following steps:

[0115] (a) applying a liquid crystal aligning agent in Example 1 on a substrate to form a coating film having a certain viscosity and a better diffusion;

[0116] (b) pre-baking at 110° C. for 90s the substrate on which the coating film is formed;

[0117] (c) baking the above-mentioned coating substrate at 230° C. for 30 min to form a liquid crystal alignment film having a thickness of 100±10 nm;

[0118] (d) irradiating the film obtained in step (c) with linearly polarized light of 254 to 313 nm, and the dose being 800 mJ, to carry out the reaction so as to form an alignment;

[0119] (e) post-baking the substrate processed in step (c) at 230° C. for 30 min to sublimate the breakdown products produced from the decomposition type alignment film.

[0120] The performance of the liquid crystal panel containing the liquid crystal alignment film was tested in accordance with the performance testing method. The test results showed that the brightness of the black state was 0.22 cd/cm.sup.2; the contrast was 2000; the disappearance time of the residual image was 0 s, and the residual image level was A.

[0121] In one embodiment, the present disclosure further provides a liquid crystal display device coated with the liquid crystal alignment film formed from the liquid crystal aligning agent as described above;

[0122] or comprising the liquid crystal alignment film as described above;

[0123] alternatively, the liquid crystal display device includes the liquid crystal alignment film prepared by the method described above.

[0124] FIG. 3a is the schematic view of the partial structure of a liquid crystal display device according to the present disclosure, wherein 301 represents a first substrate; 303 represents a second substrate; 300 is a liquid crystal layer; and the sides facing the liquid crystal layers 300 from the first substrate 301 and the second substrate 303 are coated with the liquid crystal alignment films 302 and 304 respectively. FIG. 3b is the schematic view showing a liquid crystal display device 400 having the liquid crystal alignment film according to the present disclosure. In the present embodiment, the liquid crystal display device 400 is a mobile phone. In other embodiments, the liquid crystal display device 400 may also be other types of electronic display products such as computers, televisions, watches, and vehicle display devices. The present disclosure makes no definitions to this.

[0125] The present disclosure describes the detailed processing device and process of the present disclosure, but the present disclosure is not limited to the detailed processing device and process of the present disclosure. Those skilled in the art shall know that any improvements to the present disclosure, equivalent replacement of the raw materials of the present disclosure, addition of auxiliary ingredients, selection of specific ways and the like all fall within the protection scope and disclosure scope of the present disclosure.