Abstract: A liquid crystal alignment solution is provided, including at least one polymer selected from the group consisting of a polyamide acid-polyamide acid polymer represented by formula (A), a polyimide-polyamide acid polymer represented by formula (B) and a polyimide-polyimide polymer represented by formula (C), as defined in the contexts.

Abstract: A LC compound and a LC mixture are provided. The LC mixture includes a compound represented by (I) and at least one compound selected from a group consisting of compounds represented by (II) to (IV): in which X1 is F, —Cl, —CF3, or —OCF3; R, R11, and R12 are independently H, a C1-C15 alkyl group, or a C2-C15 alkenyl group; A1 is 1,4-phenylene; A11, A12, A13, and A14 are independently selected from a group consisting of 1,4-phenylene, 1,4-cyclohexylene, and 2,5-tetrahydropyranylene; at least one of A2, A3, and A4 is 2,5-indanylene, and the others are independently selected from a group consisting of 1,4-phenylene, 1,4-cyclohexylene, and 2,5-tetrahydropyranylene; L1 is —F2CO—; Z11, Z12, and Z13 are independently a single bond, —O—, —F2CO—, or —COO—; m is 1; n, o and p are independently 0, 1, 2 or 3, and n+o+p?3.

Abstract: A LC compound and a LC mixture are provided. The LC mixture includes a compound represented by (I) and at least one compound selected from a group consisting of compounds represented by (II) to (IV): in which X1 is F, —Cl, —CF3, or —OCF3; R, R11, and R12 are independently H, a C1-C15 alkyl group, or a C2-C15 alkenyl group; A1 is 1,4-phenylene; A11, A12, A13, and A14 are independently selected from a group consisting of 1,4-phenylene, 1,4-cyclohexylene, and 2,5-tetrahydropyranylene; at least one of A2, A3, and A4 is 2,5-indanylene, and the others are independently selected from a group consisting of 1,4-phenylene, 1,4-cyclohexylene, and 2,5-tetrahydropyranylene; L1 is —F2CO—; Z11, Z12, and Z13 are independently a single bond, —O—, —F2CO—, or —COO—; m is 1; n, o and p are independently 0, 1, 2 or 3, and n+o+p?3.

Abstract: A liquid crystal alignment solution is provided. The liquid crystal alignment solution includes a first polyimide-polyamide acid and a second polyimide-polyamide acid. The first polyimide-polyamide acid is represented by formula (A), and the second polyimide-polyamide acid is represented by formula (B), in which T1, T2, T3 and T4 are each independently a tetravalent residue of a tetracarboxylic acid dianhydride; D1, D2, D3 and D4 are each independently a divalent residue of a diamine; and m, n, p and q are each independently an positive integer, wherein m/(m+n)?0.5 and p/(p+q)?0.5.

Abstract: A liquid crystal alignment solution is provided. The liquid crystal alignment solution includes at least one polymer selected from the group consisting of a polyamide acid-polyamide acid polymer represented by formula (A), a polyimide-polyamide acid polymer represented by formula (B) and a polyimide-polyimide polymer represented by formula (C), in which T1 and T2 are each independently a tetravalent organic group; m<n; p<q; r<s; and at least one of D1 and D2 is selected from the group consisting of formulae (1) to (15).

Abstract: A liquid crystal alignment solution is provided. The liquid crystal alignment solution includes a first polyimide-polyamide acid and a second polyimide-polyamide acid. The first polyimide-polyamide acid is represented by formula (A), and the second polyimide-polyamide acid is represented by formula (B), in which T1, T2, T3 and T4 are each independently a tetravalent residue of a tetracarboxylic acid dianhydride; D1, D2, D3 and D4 are each independently a divalent residue of a diamine; and m, n, p and q are each independently an positive integer, wherein m/(m+n)?0.5 and p/(p+q)?0.5.

Abstract: The invention relates to a polyimide resin polymer which contains at least one repeating unit selected from those of formula (A-1) and formula (A-2) below as polymerization units, wherein P1, P2, Q1, and Q2 are as defined in the specification. The polymer of the invention can be used as an alignment material in liquid crystal displays.

Abstract: The invention pertains to a polymer of formula (I): wherein R1, R2, R5, n and G arc as those defined in the specification. The invention also pertains to the preparation of the polymer and the use of the polymer as an alignment layer material in liquid crystal displays.

Abstract: New aromatic diamine derivatives and the preparation thereof are disclosed. The diamine derivatives of the present invention can be added to conventional polymerization reactions of tetracarboxylic acids or dianhydrides thereof and diamines to form new polyamic acids. After high-temperature baking, the polyamic acids are cyclized to form polyimides. These polyimides can be used as alignment film materials for liquid crystal display cell and have good alignment property and stability, and are effective in promoting pre-tilt angles.

Abstract: New aromatic diamine derivatives and the preparations thereof are disclosed. The inventive diamine derivatives can be added to conventional polymerization reactions of tetracarboxylic acids and diamines to form new polyamic acids. After high-temperature baking, the polyamic acids are cyclized to form polyimides. These polyimides can be used as alignment film materials for liquid crystal display cell and have good alignment property and stability, and are effective in promoting pre-tilt angle.

Abstract: New aromatic diamine derivatives and the preparation thereof are disclosed. The diamine derivatives of the present invention can be added to conventional polymerization reactions of tetracarboxylic acids or dianhydrides thereof and diamines to form new polyamic acids. After high-temperature baking, the polyamic acids are cyclized to form polyimides. These polyimides can be used as alignment film materials for liquid crystal display cell and have good alignment property and stability, and are effective in promoting pre-tilt angles.