JP2006225607A - Substituted biphenyl, terphenyl derivative and polymer thereof - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a liquid crystal compound satisfying a plural number of properties such as polymerizable at room temperature, polymerizable in air, easily polymerizable, wide in liquid crystal phase temperature range, chemically stable, colorless, easily soluble in a solvent, excellent in compatibility with other polymerizable compound, and having small adhesion tension to support substrate. <P>SOLUTION: At least one compound represented by formula (1), a composition containing the compound and a polymer obtained by polymerizing the compound are included. In formula (1), R is H or a 1-8C alkyl; A is independently a cyclic structure such as 1,4-cyclohexylene or 1,4-phenylene; G is 4,4"-terphenyl or 4,4'-biphenyl whose one or more H is substituted; Z is independently a single bond or a bond such as -(CH<SB>2</SB>)<SB>2</SB>-; and P is a 1-20C alkylene. <P>COPYRIGHT: (C)2006,JPO&NCIPI

Description

  The present invention relates to a substituted biphenyl or substituted terphenyl derivative having an oxetane ring in the side chain, a polymer obtained from this derivative, and its use.

  When the polymerizable compound is a liquid crystal, it is known that a polymer having optical anisotropy can be obtained by polymerizing the compound (Patent Document 1). This is because the orientation of molecules in the liquid crystal is fixed by polymerization. An example of such a compound is a liquid crystal compound having an acrylic group (Patent Document 2). What is further desired is a liquid crystal compound having physical properties such as polymerization at room temperature, polymerization in air, and easy polymerization by ultraviolet irradiation in the presence of a suitable photopolymerization initiator.

JP 2001-55573 A JP 2001-154019 A

  The object of the present invention is to polymerize at room temperature, polymerize in air, easily polymerize, wide temperature range of liquid crystal phase, chemically stable, colorless, easily soluble in solvents, other polymerizable compounds It is a liquid crystal compound that satisfies a plurality of properties in terms of properties such as good compatibility with the substrate and low adhesion tension to the support substrate. The problem is a compound with an appropriate balance for multiple properties. This subject is also a polymer obtained from this liquid crystal compound. This is because of the optical properties, such as optical anisotropy, difficulty in peeling from the support substrate, sufficient hardness, colorless and transparent, high heat resistance, high weather resistance, and low photoelasticity. It is also a coalescence.

The present invention includes at least one compound represented by the following formula (1), a composition containing the compound, and a polymer obtained by polymerizing the composition.

In the formula (1), R is hydrogen or alkyl having 1 to 8 carbon atoms, and in this alkyl, arbitrary hydrogen may be replaced by fluorine or chlorine; A is independently 1,4-cyclohexylene, 1,4-phenylene, pyridine-2,5-diyl, pyridazine-3,6-diyl, pyrimidine-2,5-diyl, naphthalene-2,6-diyl, or tetrahydronaphthalene-2,6-diyl; In this 1,4-phenylene, any hydrogen may be replaced by fluorine or chlorine, and any one or two hydrogens may be cyano, methyl, ethyl, methoxy, hydroxy, formyl, acetoxy, acetyl, trifluoroacetyl. , Difluoromethyl, or trifluoromethyl; G is at least one hydrogen chloride 4,4 "-terphenyl or at least one hydrogen substituted with fluorine, methyl, ethyl, isopropyl, methoxy, hydroxy, formyl, acetoxy, acetyl, trifluoroacetyl, difluoromethyl, or trifluoromethyl is chlorine, fluorine, 4,4′-biphenyl substituted with methyl, ethyl, isopropyl, methoxy, hydroxy, formyl, acetoxy, acetyl, trifluoroacetyl, difluoromethyl, or trifluoromethyl; Z is independently a single bond, — (CH ₂ ) ₂ , —CH═CH—, —C≡C—, —CH ₂ O—, —OCH ₂ —, —CF ₂ O—, —OCF ₂ —, —COO—, —OCO—, —CONH—, _{-NHCO -, - (CH 2)} 4 -, - (CH 2) 2 COO -, - OCO (CH 2) 2 , —CH═CH—COO—, or —OCO—CH═CH—; P is alkylene having 1 to 20 carbons, and in this alkylene, any hydrogen may be replaced by fluorine or chlorine, —CH ₂ — may be replaced with —O—, any one or two —CH ₂ — may be replaced with —COO— or —OCO—, and any one —CH _{2 —.} -May be replaced by -CH = CH- or -C≡C-.

  The liquid crystal compound of the present invention is polymerized at room temperature, polymerized in air, easily polymerized, wide temperature range of liquid crystal phase, chemically stable, colorless, easily soluble in solvent, other polymerizable compounds A plurality of characteristics are satisfied with respect to characteristics such as good compatibility with and low adhesion tension to the support substrate. This compound has an appropriate balance for multiple properties. The polymer of the present invention is obtained from this liquid crystal compound. This polymer has physical properties such as optical anisotropy, difficulty in peeling from the support substrate, sufficient hardness, colorless and transparent, high heat resistance, high weather resistance, and low photoelasticity. .

  Terms used in this specification are as follows. A liquid crystal compound is a generic term for a compound having a liquid crystal phase and a compound having no liquid crystal phase but useful as a component of a liquid crystal composition. The liquid crystal phase is a nematic phase, a smectic phase, a cholesteric phase or the like, and often means a nematic phase. Polymerizability means the ability of a monomer to polymerize and give a polymer by means such as light, heat, or catalyst. A compound represented by formula (1), formula (M1), or the like may be represented as compound (1), compound (M1), or the like. A polymer obtained from a composition containing the compound (1) or the like may be referred to as a polymer (1). A polymer obtained from a composition containing the compound (2) or the like may be referred to as a polymer (2).

  We have two findings: 1) polymerizing a polymerizable liquid crystal compound to obtain a polymer having optical anisotropy, and 2) a monomer having an oxetane ring easily undergoes ring-opening polymerization. Inspired to combine. When research was conducted based on this idea, the experimental results were better than expected. Based on these results, studies were repeated and the present invention including the following items was completed.

1. The compound represented by Formula (1).

  In the formula (1), symbols such as R, P, A, G, Z, B, Q, and Y are used. The meanings of the two symbols R may be the same or different. This rule also applies to symbols P, A, G, Z, B, Q, and Y. This rule also applies to other expressions.

  In the formula (1), R is hydrogen or alkyl having 1 to 8 carbon atoms, and in this alkyl, arbitrary hydrogen may be replaced with fluorine or chlorine. Preferred R is hydrogen or alkyl having 1 to 5 carbons. Particularly preferred R is methyl or ethyl.

  A is independently 1,4-cyclohexylene, 1,4-phenylene, pyridine-2,5-diyl, pyridazine-3,6-diyl, pyrimidine-2,5-diyl, naphthalene-2,6-diyl. Or tetrahydronaphthalene-2,6-diyl in which any hydrogen may be replaced by fluorine or chlorine and any one or two hydrogens may be cyano, methyl, ethyl, It may be replaced with methoxy, hydroxy, formyl, acetoxy, acetyl, trifluoroacetyl, difluoromethyl, or trifluoromethyl.

  Preferred A is independently 1,4-phenylene, 2-fluoro-1,4-phenylene, 2-chloro-1,4-phenylene, 2-methyl-1,2-trifluoromethyl-1,4-phenylene, 2,3-difluoro-1,4-phenylene, 2,5-difluoro-1,4-phenylene, 2,6-difluoro-1,4-phenylene, 2,3,5-trifluoro-1,4-phenylene Or 2,3,5,6-tetrafluoro-1,4-phenylene.

  Particularly preferred A is independently 1,4-phenylene, 2-fluoro-1,4-phenylene, 2-chloro-1,4-phenylene, 2-methyl-1,4-phenylene, 2,3-difluoro-1 , 4-phenylene, 2,5-difluoro-1,4-phenylene, 2,6-difluoro-1,4-phenylene.

  G is 4,4 ″ -terphenyl in which at least one hydrogen is replaced by chlorine, fluorine, methyl, ethyl, isopropyl, methoxy, hydroxy, formyl, acetoxy, acetyl, trifluoroacetyl, difluoromethyl, or trifluoromethyl, or At least one hydrogen is 4,4′-biphenyl substituted with chlorine, fluorine, methyl, ethyl, isopropyl, methoxy, hydroxy, formyl, acetoxy, acetyl, trifluoroacetyl, difluoromethyl, or trifluoromethyl.

  Preferred G is 4,4 "-terphenyl in which at least one hydrogen is replaced by chlorine, fluorine, methyl, ethyl, or trifluoromethyl or at least one hydrogen is chlorine, fluorine, methyl, ethyl, or trifluoromethyl Substituted 4,4′-biphenyl.

More preferable G is any one of the following formulas (G-1) to (G-15). Particularly preferred G is any one of formulas (G-1) to (G-4) and formulas (G-8) to (G-11).

Z is independently a single bond, — (CH ₂ ) ₂ —, —CH═CH—, —C≡C—, —CH ₂ O—, —OCH ₂ —, —CF ₂ O—, —OCF ₂ —, _{-COO -, - OCO -, -} CONH -, - NHCO -, - (CH 2) 4 -, - (CH 2) 2 COO -, - OCO (CH 2) 2 -, - CH = CH-COO-, Or -OCO-CH = CH-.

Preferred Z is independently a single bond, — (CH ₂ ) ₂ —, —C≡C—, —CH ₂ O—, —OCH ₂ —, —COO—, —OCO—, —CONH—, —NHCO—, _{- (CH 2) 4 -,} - (CH 2) 2 COO -, - OCO (CH 2) 2 -, - CH = CH-COO-, or -OCO-CH = CH- it is. Particularly preferred Z is independently —COO—, —OCO—, — (CH ₂ ) ₂ COO—, —OCO (CH ₂ ) ₂ —, —CH═CH—COO—, or —OCO—CH═CH—. is there.

P is alkylene having 1 to 20 carbon atoms, in which any hydrogen may be replaced with fluorine or chlorine, and any —CH ₂ — may be replaced with —O—, Or two —CH ₂ — may be replaced with —COO— or —OCO—, and any one —CH ₂ — may be replaced with —CH═CH— or —C≡C—.

Preferred P is —O—, —O— (CH ₂ ) r—, — (CH ₂ ) r—O—, — (CH ₂ ) r—, —O— (CH ₂ ) r—O—, or —O - _{(CH 2} CH 2 O) a s-, r is an integer of 1 to 15, and s is an integer from 1 to 5. Particularly preferred P is —O— or —O— (CH ₂ ) r—O—, and r is an integer of 2 to 10.

Ｚが独立して単結合、−（ＣＨ_２）_２−、−Ｃ≡Ｃ−、−ＣＨ_２Ｏ−、−ＯＣＨ_２−、−ＣＯＯ−、−ＯＣＯ−、−ＣＯＮＨ−、−ＮＨＣＯ−、−（ＣＨ_２）_４−、−（ＣＨ_２）_２ＣＯＯ−、−ＯＣＯ（ＣＨ_２）_２−、−ＣＨ＝ＣＨ−ＣＯＯ−、または−ＯＣＯ−ＣＨ＝ＣＨ−であり；Ｐが炭素数１〜１７のアルキレンであり、このアルキレンにおいて任意の−ＣＨ_２−は−Ｏ−で置き換えられてもよく、任意の１つまたは２つの−ＣＨ_２−は−ＣＯＯ−または−ＯＣＯ−で置き換えられてもよく、そして任意の１つの−ＣＨ_２−は−ＣＨ＝ＣＨ−で置き換えられてもよい項１または２に記載の化合物。
４． 下記の式（２）〜（９）のいずれか１つで表される化合物。

2. In the formula (1), R is hydrogen or alkyl having 1 to 5 carbon atoms, and in this alkyl, arbitrary hydrogen may be replaced by fluorine or chlorine; A is independently 1,4-phenylene; In this 1,4-phenylene, any hydrogen may be replaced with fluorine or chlorine, and any one or two hydrogens may be replaced with methyl, ethyl or trifluoromethyl; G is at least one 4,4 "-terphenyl substituted with chlorine, fluorine, methyl, ethyl, or trifluoromethyl or 4,4 substituted with at least one hydrogen with chlorine, fluorine, methyl, ethyl, or trifluoromethyl '- biphenyl; Z is independently a single _{bond, - (CH 2) 2 -} , - C≡C -, - CH 2 O -, - OCH 2 -, - C _{O -, - OCO -, -} CONH -, - NHCO -, - (CH 2) 4 -, - (CH 2) 2 COO -, - OCO (CH 2) 2 -, - CH = CH-COO-, or -OCO-CH = CH- and is; P is alkylene of 1 to 17 carbon atoms, any in the alkylene -CH ₂ - may be replaced by -O-, any one or two - Item 2. The compound according to Item 1, wherein CH ₂ — may be replaced with —COO— or —OCO—, and any one —CH ₂ — may be replaced with —CH═CH—.
3. In the formula (1), R is hydrogen or alkyl having 1 to 5 carbon atoms, and in this alkyl, arbitrary hydrogen may be replaced by fluorine or chlorine; A is independently 1,4-phenylene; In this 1,4-phenylene, any hydrogen may be replaced with fluorine or chlorine, and any one or two hydrogens may be replaced with methyl, ethyl, or trifluoromethyl; Having

Z is independently a single bond, — (CH ₂ ) ₂ —, —C≡C—, —CH ₂ O—, —OCH ₂ —, —COO—, —OCO—, —CONH—, —NHCO—, — (CH ₂ ) ₄ —, — (CH ₂ ) ₂ COO—, —OCO (CH ₂ ) ₂ —, —CH═CH—COO—, or —OCO—CH═CH—; 17 alkylene, in which any —CH ₂ — may be replaced by —O—, and any one or two —CH ₂ — may be replaced by —COO— or —OCO—. Item 3. The compound according to Item 1 or 2, wherein any one of —CH ₂ — may be replaced by —CH═CH—.
4). The compound represented by any one of following formula (2)-(9).

In the above formula, R is alkyl having 1 to 5 carbon atoms; A is independently 1,4-phenylene, 2-fluoro-1,4-phenylene, 2-chloro-1,4-phenylene, 2-methyl. -1,2-trifluoromethyl-1,4-phenylene, 2,3-difluoro-1,4-phenylene, 2,5-difluoro-1,4-phenylene, 2,6-difluoro-1,4-phenylene 2,3,5-trifluoro-1,4-phenylene, or 2,3,5,6-tetrafluoro-1,4-phenylene; Z is independently a single bond, — (CH ₂ ) ₂ —, —C≡C—, —CH ₂ O—, —OCH ₂ —, —COO—, —OCO—, —CONH—, —NHCO—, — (CH ₂ ) ₄ —, — (CH ₂ ) ₂ COO _{-, - OCO (CH 2)} 2 -, - CH = CH-COO Or -OCO-CH = CH- and is,; -, - P is _{-O O- (CH 2) r -} , - (CH 2) r-O -, - (CH 2) r -, - O- ( A compound wherein CH ₂ ) r—O—, or —O— (CH ₂ CH ₂ O) s—, r is an integer from 1 to 15, and s is an integer from 1 to 5.

5. In formulas (2) to (9), R is methyl or ethyl; A is independently 1,4-phenylene, 2-fluoro-1,4-phenylene, 2-chloro-1,4-phenylene, 2 -Methyl-1,4-phenylene, 2,3-difluoro-1,4-phenylene, 2,5-difluoro-1,4-phenylene, or 2,6-difluoro-1,4-phenylene; Independently —COO—, —OCO—, — (CH ₂ ) ₂ COO—, —OCO (CH ₂ ) ₂ —, —CH═CH—COO— or —OCO—CH═CH—; Item 5. The compound according to Item 4, wherein the compound is O— or —O— (CH ₂ ) r—O—, and r is an integer of 2 to 10.

6). In formulas (2) to (9), R is methyl or ethyl; A is independently 1,4-phenylene, 2-fluoro-1,4-phenylene, 2-chloro-1,4-phenylene, 2 -Methyl-1,4-phenylene, 2,3-difluoro-1,4-phenylene, 2,5-difluoro-1,4-phenylene, or 2,6-difluoro-1,4-phenylene; Independently —COO—, —OCO—, — (CH ₂ ) ₂ COO—, or —OCO (CH ₂ ) ₂ —; P is —O— (CH ₂ ) r—O—, and r Item 5. The compound according to Item 4, wherein is an integer of 2 to 10.

7). In formulas (2) to (9), R is methyl or ethyl; A is independently 1,4-phenylene, 2-fluoro-1,4-phenylene, 2-chloro-1,4-phenylene, or 2-methyl-1,4-phenylene; Z is independently —COO—, —OCO—, — (CH ₂ ) ₂ COO—, or —OCO (CH ₂ ) ₂ —; P is —O Item 5. The compound according to Item 4, which is — (CH ₂ ) r—O—, and r is an integer of 2 to 10.

8). In formulas (2) to (9), R is methyl; A is independently 1,4-phenylene; Z is independently —COO— or —OCO—; P is —O— ( Item 5. The compound according to Item 4, wherein the compound is CH ₂ ) r—O—, and r is an integer of 2 to 10.

9. In formulas (2) to (9), R is ethyl; A is independently 1,4-phenylene; Z is independently —COO— or —OCO—; P is —O— ( Item 5. The compound according to Item 4, wherein the compound is CH ₂ ) r—O—, and r is an integer of 2 to 10.

10. Item 10. A composition containing at least one compound according to any one of Items 1 to 9 as a first component.

11. Item 11. The composition according to Item 10, further comprising a polymerizable compound different from the compound according to any one of Items 1 to 9 as a second component.

式（Ｍ１）〜式（Ｍ４）において、Ｒａは水素、フッ素、塩素、−ＣＮ、−ＯＣＦ_３、炭素数１〜２０のアルキル、炭素数１〜２０のアルコキシ、炭素数２〜２０のアルコキシアルキル、炭素数２〜２０のアルケニル、または炭素数２〜２０のアルケニルオキシであり；Ｒｂは水素または炭素数１〜５のアルキルであり；Ｂは独立して１，４−シクロへキシレンまたは１，４−フェニレンであり、この１，４−フェニレンにおいて任意の水素はフッ素で置き換えられてもよく、そして任意の１つまたは２つの水素はメチルまたはトリフルオロメチルで置き換えられてもよく、そしてＢの１つはナフタレン−２，６−ジイル、フルオレン−２，７−ジイル、９−メチルフルオレン−２，７−ジイル、９−エチルフルオレン−２，７−ジイル、９，９−ジメチルフルオレン−２，７−ジイル、９−クロロフルオレン−２，７−ジイル、または９，９−ジフルオロフルオレン−２，７−ジイルであってもよく；Ｙは独立して単結合、−ＣＯＯ−、−ＯＣＯ−、−（ＣＨ_２）_２−、または−Ｃ≡Ｃ−であり；Ｑは独立して単結合または炭素数１〜２０のアルキレンであり、このアルキレンにおいて１つまたは２つの−ＣＨ_２は−Ｏ−で置き換えられてもよく；そしてｔは１または２である。 12 The composition according to claim 10, wherein the second component is at least one compound selected from the group of compounds represented by formula (M1), formula (M2), formula (M3) and formula (M4).

In the formulas (M1) to (M4), Ra is hydrogen, fluorine, chlorine, —CN, —OCF ₃ , alkyl having 1 to 20 carbons, alkoxy having 1 to 20 carbons, or alkoxyalkyl having 2 to 20 carbons. , Alkenyloxy having 2 to 20 carbons, or alkenyloxy having 2 to 20 carbons; Rb is hydrogen or alkyl having 1 to 5 carbons; B is independently 1,4-cyclohexylene or 1, 4-phenylene, in which any hydrogen may be replaced by fluorine, and any one or two hydrogens may be replaced by methyl or trifluoromethyl, and B One is naphthalene-2,6-diyl, fluorene-2,7-diyl, 9-methylfluorene-2,7-diyl, 9-ethylfluorene-2,7-diyl, , 9-dimethylfluorene-2,7-diyl, 9-chlorofluorene-2,7-diyl, or 9,9-difluorofluorene-2,7-diyl; Y is independently a single bond, —COO—, —OCO—, — (CH ₂ ) ₂ —, or —C≡C—; Q is independently a single bond or alkylene having 1 to 20 carbons, and in this alkylene, one or two Two —CH ₂ may be replaced by —O—; and t is 1 or 2.

13. In the formulas (M1) to (M4), Ra is fluorine, chlorine, —CN, —OCF ₃ , alkyl having 1 to 15 carbons, or alkoxy having 2 to 15 carbons; Rb is hydrogen or 1 carbon ~ 2 alkyl; B is independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 2-chloro-1,4-phenylene, 2-methyl- 1,4-phenylene, 2,3-difluoro-1,4-phenylene, 2,5-difluoro-1,4-phenylene, 2,6-difluoro-1,4-phenylene, 9-methylfluorene-2,7 -Diyl, 9,9-dimethylfluorene-2,7-diyl or 9-ethylfluorene-2,7-diyl; Y is independently a single bond, -COO-, -OCO-, or- C≡C- Q is independently a single bond or alkylene having 1 to 10 carbon atoms, in the alkylene one or two -CH 2 _- may be replaced by -O-; and t is 1 or 2 wherein Item 13. The composition according to Item 12.

14 In the formulas (M1) to (M4), Ra is fluorine, chlorine, —OCF ₃ , alkyl having 1 to 10 carbons, or alkoxy having 2 to 10 carbons; Rb is hydrogen or having 1 to 2 carbons B is independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 2-chloro-1,4-phenylene, 2-methyl-1,4 -Phenylene, 2,3-difluoro-1,4-phenylene, 2,5-difluoro-1,4-phenylene, 2,6-difluoro-1,4-phenylene, 9-methylfluorene-2,7-diyl, May be 9,9-dimethylfluorene-2,7-diyl or 9-ethylfluorene-2,7-diyl; Y is independently a single bond, —COO—, —OCO—, or —C≡C; -Is; Q is German A single _{bond, - (CH 2) m -} , - (CH 2) m-O-, or -O- _(CH 2) a m-, m is an integer from 1 to 10; and t is 1 or 2 Item 13. The composition according to Item 12, wherein

15. The second component is selected from at least one compound selected from the group of compounds represented by Formula (M1) and Formula (M2), or a group of compounds represented by Formula (M3) and Formula (M4) Item 12. The composition according to Item 10 or 11, which is a compound.

16. Item 12. The composition according to item 10 or 11, wherein the second component is a compound selected from the group of compounds represented by formula (M1) or formula (M2).

17. Item 10. A polymer obtained by polymerizing the compound according to any one of Items 1 to 9.

18. Item 17. A polymer obtained by polymerizing the composition according to any one of Items 10 to 16.

19. Item 10. A polymer obtained by orienting the compound according to any one of items 1 to 9 or the composition according to any one of items 10 to 16, and then polymerizing while maintaining the orientation.

20. A film obtained by orienting the compound according to any one of items 1 to 9 or the composition according to any one of claims 10 to 16 and then polymerizing while maintaining the orientation.

  The compounds of the present invention have the following characteristics. This compound polymerizes at room temperature, polymerizes in air, is easy to polymerize, has a wide liquid crystal phase temperature range, is chemically stable, is colorless, is soluble in solvents, and is compatible with other polymerizable compounds. It has characteristics such as good solubility and low adhesion tension to the support substrate. This compound has a liquid crystal phase. This liquid crystal phase has a wide temperature range. The molecular orientation in the liquid crystal phase is maintained by polymerization. That is, the molecular orientation is fixed by polymerization. The polymerization of the liquid crystal compound having an acrylic group is preferably carried out in an atmosphere of nitrogen, but this compound may be polymerized in air. This compound is easily polymerized in the presence of a suitable photopolymerization initiator even when irradiated with a small cumulative amount of ultraviolet light. Since this compound is chemically stable, it has excellent storage stability. Since this compound has good compatibility with other polymerizable compounds, compositions having various compositions can be obtained. Since this compound has good wettability with respect to the support substrate, it is easy to obtain a uniform paint film. Of these, important are the characteristics such as polymerization in the air, easy polymerization, wide temperature range of the liquid crystal phase, and easy uniform coating.

  A polymer obtained from such a compound has the following characteristics. This polymer has optical anisotropy, is difficult to peel from the support substrate, has sufficient hardness, has high heat resistance, is colorless and transparent, has high weather resistance, has low photoelasticity, etc. Has physical properties. This polymer is also excellent in properties such as impact resistance, processability, electrical properties, and solvent resistance. Of these, important characteristics are characteristics such as difficulty in peeling from the support substrate, sufficient hardness, and high heat resistance.

  Compound (1) is a liquid crystal compound having an oxetane ring. These compounds are polymerizable and are stable under normal handling conditions. These compounds are easily polymerized at room temperature even in an air atmosphere by irradiation with ultraviolet rays or the like in the presence of a photocationic polymerization catalyst. The compound (1) is easily aligned by an alignment film or the like. Therefore, the obtained polymer has no or few alignment defects.

  Compound (1) has a large dielectric anisotropy, a small dielectric anisotropy and a large optical anisotropy by appropriately selecting the side chain R, ring A, ring B, linking group Z, and spacer P. The physical properties such as small optical anisotropy and small viscosity can be adjusted.

When P is —O— (CH ₂ ) r—O—, the larger the number of r, the lower the melting point of the compound (1). When R is alkyl, monomers having a small number of carbons tend to give large heat resistant polymers.

  When A is 1,4-cyclohexylene, the optical anisotropy of the monomer is small. When A is 1,4-phenylene, the optical anisotropy of the monomer is large. When at least one of X is —COO— or —OCO—, the compound (1) has better liquid crystallinity. When at least one of X is —C≡C—, the compound (1) has a large optical anisotropy. When P has oxygen (—O—), the optical anisotropy of the monomer is large.

Compound (1) may contain an isotope element such as ² H (deuterium) or ¹³ C in an amount higher than that naturally occurring. Even in such a case, there is no significant difference in the physical properties of the compounds.

  The physical properties of the compound (1) are reflected in the physical properties of the polymer (1). Among the physical properties, optical anisotropy is important for the purpose of the present invention. When the composition containing the compound (1) is polymerized on the support substrate, the obtained polymer is difficult to peel from the support substrate. Since the compounds (3) to (6) have a low viscosity, they are suitable for reducing the viscosity of the composition. Since the compound (7) or (8) has a wide temperature range of the liquid crystal phase, it is suitable for expanding the temperature range of the liquid crystal phase in the composition.

  Preferred compounds (1) are compounds (2) to (9). Particularly preferred compounds (1) are compounds (2a) to (9a), compounds (2b) to (9b), and compounds (2c) to (9c).

In these formulas, R is methyl or ethyl, P is —O— or —O— (CH ₂ ) r—O—, and r is an integer from 2 to 10, W ¹⁷ or W ¹⁸ is Chlorine, fluorine, methyl or trifluoromethyl.

  Next, a synthesis method of compound (1) will be described. Compound (1) includes Houben Wyle, Methoden der Organischen Chemie, Georg Thieme Verlag, Stuttgart, Organic Reactions (Organic Reactions, John Wily & Sons Inc.), Organic Syntheses (John Wily & Sons, Inc.), Comprehensive Organic Synthesis (Pergamon Press), New Experimental Chemistry Course (Maruzen), etc., can be synthesized by appropriately combining synthetic methods in organic chemistry.

For the oxetane ring, 3-alkyl-3-oxetanemethanol can be used as a starting material. 3-ethyl-3-oxetanemethanol and 3-methyl-3-oxetanemethanol are commercially available. By reacting these compounds with α, ω-dibromomethylene such as 1,2-dibromoethane, 1,4-dibromobutane, 1,6-dibromohexane, 1,8-dibromooctane according to literature methods. , Can extend the chain length. The literature is Macromolecules, 24 , 4531-4537 (1991). A method for producing the linking group X is disclosed in JP-A-2003-277359 (paragraphs 0040 to 0053). A method for producing a linking group X connected to a fluorene ring is disclosed in JP-A-2003-238491 (paragraphs 0019 to 0038). The synthesis scheme of compound (1) is illustrated.

Scheme 1.

Compounds (2a) to (5a) in combinations where Z is —COO— and —OOC—, and compounds (2b) to (5b) in combinations where Z is —CH═CH—COO— and —OCO—CH═CH—. ), And the synthesis of compounds (2c) to (5c), which is a combination of compounds in which Z is — (CH ₂ ) ₂ COO— and —OCO (CH ₂ ) ₂ —, is shown in Scheme 2. In the scheme, Bn represents a benzyl group, and K represents a single bond, — (CH ₂ ) ₂ — or —CH═CH—.
4-Benzyloxybromobenzene derivative [a1] is converted into a Grignard reagent with magnesium metal and reacted with trimethylborate to give the corresponding boronic acid derivative [b]. A cross-coupling reaction between the boronic acid derivative [b] and the dibromobenzene derivative [c] is performed to obtain a coupled product [d]. A palladium catalyst is used for the coupling reaction. The coupling product [d] is hydrocracked in the presence of a palladium catalyst to obtain the corresponding dihydroxyterphenyl derivative [e]. The dihydroxyterphenyl derivative [e] and 2 equivalents of the compound [f] are reacted to synthesize the compounds (2) to (5).

Scheme 2

An alternative method is shown in Scheme 2. A cross-coupling reaction between the boronic acid derivative [b] and 4-bromo-4′-benzyloxybiphenyl [i] is performed to obtain a coupled product. The coupling product is hydrocracked in the presence of a palladium catalyst to give the corresponding dihydroxyterphenyl derivative. Compounds (2) to (5) are synthesized by reacting a dihydroxyterphenyl derivative with 2 equivalents of compound [f].

Scheme 3

Compounds (6a) to (9a) in combinations where Z is —COO— and —OOC—, and compounds (6b) to (9b) in which Z is —CH═CH—COO— and —OCO—CH═CH—. ), And the synthesis of compounds (6c) to (9c), which is a combination of compounds in which Z is — (CH ₂ ) ₂ COO— and —OCO (CH ₂ ) ₂ —, is shown in Scheme 3.
A cross-coupling reaction between the boronic acid derivative [b] and 4-bromophenol [a2] in which the hydroxyl group is protected with benzyl (in the scheme; represented by benzyl = Bn) is performed to obtain a coupled product [d]. A palladium catalyst is used for the coupling reaction. The coupling body [g] is hydrocracked in the presence of a palladium catalyst to obtain the corresponding dihydroxybiphenyl derivative [h]. Compounds (6) to (9) are synthesized by reacting the dihydroxybiphenyl derivative [h] with 2 equivalents of the compound [f].

Scheme 4

Dihydroxybiphenyl [h] can also be synthesized from biphenyl derivative [j] by acetylation by Friedel-Crafts reaction, Bayer-bilger reaction by peroxide, and hydrolysis route (Scheme 4)

R in the schemes 1 to 4 is methyl or ethyl, K is a single bond, —CH═CH— or — (CH ₂ ) ₂ —, and V ^{1 to} V ¹⁶ are hydrogen, chlorine, fluorine. , Methyl and trifluoromethyl. However, all of V ^{1 to} V ¹⁶ are not hydrogen. V ¹⁷ or V ¹⁸ is hydrogen, chlorine, fluorine, methyl, trifluoromethyl.
Examples of compounds synthesized by such methods include Compound No. 1-No. 56.

  Next, the composition of the present invention will be described. This composition contains the compound (1) as a first component. This composition usually means a mixture of a plurality of compounds, but even one compound (1) may be referred to as a composition. By polymerizing the composition containing the first component, a polymer having optical anisotropy is obtained. The polymerizable compound may be only the first component. This composition is classified into the following compositions A, B, C, D and the like. Composition A contains one compound selected from the group of compounds (1). Composition B contains at least two compounds selected from the group of compounds (1). Composition C contains at least one compound selected from the group of compounds (1) as the first component and at least one compound selected from the group of other polymerizable compounds as the second component. Composition D is Composition A, B or C which further contains a non-polymerizable compound.

  The “other polymerizable compound” is a polymerizable compound (monomer) different from the compound (1). Other polymerizable compounds are useful for improving or modifying the properties of the resulting polymer. Other polymerizable compounds may be optically active or optically inactive. Preferred examples of the optically inactive polymerizable compound include a compound having an oxiranyl group, a compound having an oxetanyl group, a compound having a vinyl ether group, a compound having a vinyl group, a compound having an acrylic group, and a compound having a methacryl group Etc. Examples of these compounds are described in JP-A-8-3111.

  Preferred second components in the composition C are the compounds (M1) to (M4) already described. Composition C comprises ethyl vinyl ether, hydroxybutyl monovinyl ether, t-amyl vinyl ether, cyclohexanedimethanol methyl vinyl ether, 3-ethyl-3-hydroxymethyl oxetane, 3-methyl-3-hydroxymethyl oxetane, di (3-ethyl- It may further contain a compound such as oxeta-3-ylmethyl), 3-ethyl-3- (2-ethylhexyloxymethyl) oxetane. These compounds are suitable for adjusting the viscosity of the composition. These compounds have a great effect of making the thickness of the coating film uniform when the composition is applied. The polymerizable optically active compound induces a helical structure in the liquid crystal phase. Compounds with a large helical twist power are preferred. Preferred examples of the polymerizable optically active compound are compounds (OP1) to (OP14).

In these formulas (OP1) to (OP13): R ⁶ is methyl or ethyl, W ¹ and W ² are each independently hydrogen, chlorine, fluorine, or cyano, and W ³ and W ⁴ Are each independently hydrogen, chlorine, fluorine, cyano, methyl or trifluoromethyl, X ⁶ is independently a single bond or —O—, and o, p and r are each independently 0 It is an integer of ~ 20. * Indicates an asymmetric position. Compounds (OP10) to (OP14) are axially asymmetric.

  The composition D contains a non-polymerizable compound such as a liquid crystal compound or an optically active compound. Examples of liquid crystal compounds are described in a liquid crystal compound database (registered trademark: LiqCryst) sold by Fujitsu Kyushu Engineering. Such a compound can be expected to play a role of adjusting the viscosity of the composition and adjusting the temperature range of the liquid crystal phase. The role of adjusting the pitch of optically active compounds and compositions can be expected.

  A preferred composition contains at least one of the compounds (1) as a first component and at least one of the compounds (M1) to (M4) as a second component. This second component compound has a polymerizable group suitable for copolymerization with the compound (1). Preferred compounds (M1) to (M4) are compounds (M1a) to (M4c).

In these formulas: R ⁵ is fluorine, chlorine, —OCF ₃ , alkyl having 1 to 10 carbons, or alkoxy having 2 to 10 carbons, R ⁶ is hydrogen, methyl or ethyl, and W ¹ and W ² is independently hydrogen or fluorine, W ³ and W ⁴ are independently hydrogen, fluorine, methyl or trifluoromethyl, and X ⁵ and X ⁶ are independently a single bond or —O—. , M and n are each independently an integer of 1 to 10.

  When the first component is at least one of the compounds (1) and the second component is at least one of the compounds (M1) to (M4), examples of preferred combinations are compositions (C1) to (C6 ). Preferred compositions are summarized in Table 1. The compounds (M1) to (M4) are used to adjust the temperature range of the liquid crystal phase, the viscosity, the orientation of the liquid crystal phase, the film-forming property in the polymer, the mechanical strength, the adhesion to the support substrate, and the like. convenient. The content of the first component is 1 to 99% by weight, more preferably 5 to 95% by weight. The content of the second component is 1 to 99% by weight, more preferably 10 to 95% by weight.

Table 1. Preferred composition

  The features of the compositions (C1) to (C6) are as follows. 1) A polymer can be easily obtained by irradiating the composition with ultraviolet rays in the presence of an appropriate photocationic polymerization catalyst. 2) Polymerization proceeds not only in an atmosphere of nitrogen but also in air. 3) When it becomes a polymer (film) from a composition, it is hard to become small in size. Among compositions (C1) to (C6), particularly preferred examples are compositions (C1), (C2), and (C3). The characteristics of these compositions are as follows. 1) Polymerization is fast and a high molecular weight film can be obtained in a short time. 2) A film excellent in dimensional stability can be obtained. 3) A film excellent in heat resistance can be obtained.

  Compositions such as A, B, C, and D may further contain additives as necessary. Additives for adjusting the physical properties of the polymer include surfactants, antioxidants, ultraviolet absorbers, and fine particles. Additives for polymerizing the monomer include a polymerization initiator and a photosensitizer. Organic solvents are preferred for diluting the composition. The amount of these additives is preferably small enough to achieve the purpose.

  The surfactant has effects such as easy application of the composition to a support substrate and the like, and controlling the orientation of the liquid crystal phase. Examples of surfactants include quaternary ammonium salts, alkylamine oxides, polyamine derivatives, polyoxyethylene-polyoxypropylene condensates, polyethylene glycol and esters thereof, sodium lauryl sulfate, ammonium lauryl sulfate, lauryl sulfate amines, alkyl-substituted fragrances. Group sulfonates, alkyl phosphates, perfluoroalkyl sulfonates, perfluoroalkyl carboxylates, perfluoroalkyl ethylene oxide adducts, perfluoroalkyl trimethyl ammonium salts, and the like. The preferable amount of the surfactant varies depending on the kind of the surfactant, the composition ratio of the composition, and the like, but is in the range of 100 ppm to 5% by weight based on the weight of the photopolymerizable liquid crystal composition. A more preferred amount is in the range of 0.1 to 1% by weight.

  Preferred antioxidants are hydroquinone, 2,6-di-t-butyl-p-cresol, 2,6-di-t-butylphenol, triphenyl phosphite, trialkyl phosphite and the like. Preferred commercial products are Irganox 245 and Irganox 1035 manufactured by Ciba Specialty.

  Preferred UV absorbers are Tinuvin PS, Tinuvin 213, Tinuvin 109, Tinuvin 328, Tinuvin 384-2, Tinuvin 327, etc., manufactured by Ciba Specialty.

Fine particles may be added to adjust the optical anisotropy or increase the strength of the polymer. Preferred fine particle materials are inorganic, organic, metal, and the like. Preferred inorganic materials are ceramics, fluorine phlogopite, tetrasilica mica, teniolite, fluorine vermiculite, fluorine hectorite, hectorite, saponite, stevensite, montmorillonite, beidellite, kaolinite, frypontite, ZnO, TiO ₂ , CeO ₂ , Al ₂ O ₃ , Fe ₂ O ₃ , ZrO ₂ , MgF ₂ , SiO ₂ , SrCO ₃ , Ba (OH) ₂ , Ca (OH) ₂ , Ga (OH) ₃ , Al (OH) ₃ , Mg (OH) ₂ , Zr (OH) ₄ and the like. Fine particles such as calcium carbonate needle crystals have optical anisotropy. Such fine particles can adjust the optical anisotropy of the polymer.

  Preferred organic materials are carbon nanotubes, fullerenes, dendrimers, polyvinyl alcohol, polymethacrylates, polyimides and the like. The preferred particle size of the fine particles is 0.001 to 0.1 μm. A more preferable particle size is 0.001 to 0.05 μm. Depending on the material, a small particle size is preferred to prevent agglomeration. Sharper particle size distribution is preferred. A preferable addition amount is 0.1 to 30% by weight. A small proportion is preferable as long as the purpose of addition is achieved.

  A preferred polymerization initiator is an initiator for photocationic polymerization. This initiator is particularly suitable for the compositions (C1) to (C13). Preferred initiators include diaryliodonium salts (hereinafter abbreviated as DAS), triarylsulfonium salts (hereinafter abbreviated as TAS), and the like.

  Examples of DAS are diphenyliodonium tetrafluoroborate, diphenyliodonium hexafluorophosphonate, diphenyliodonium hexafluoroarsenate, diphenyliodonium tetra (pentafluorophenyl) borate, 4-methoxyphenylphenyliodonium tetrafluoroborate, 4-methoxyphenylphenyliodonium Hexafluorophosphonate, 4-methoxyphenylphenyl iodonium hexafluoroarsenate, bis (4-tert-butylphenyl) iodonium diphenyliodonium tetrafluoroborate, bis (4-tert-butylphenyl) iodonium diphenyliodonium hexafluoroarsenate, bis ( 4-tert-butylphenyl) iodonium di E sulfonyl iodonium trifluoromethanesulfonate and the like.

  A combination of DAS and photosensitizer is preferred. Examples of photosensitizers are thioxanthone, phenothiazine, chlorothioxanthone, xanthone, anthracene, diphenylanthracene, rubrene and the like.

  Examples of TAS are triphenylsulfonium hexafluorophosphonate, triphenylsulfonium hexafluoroarsenate, triphenylsulfonium tetra (pentafluorophenyl) borate, 4-methoxyphenyldiphenylsulfonium tetrafluoroborate, 4-methoxyphenyldiphenylsulfonium hexafluorophosphonate 4-methoxyphenyldiphenylsulfonium hexafluoroarsenate, 4-methoxyphenyldiphenylsulfonium trifluoromethanesulfonate, 4-methoxyphenyldiphenylsulfonium triphenylsulfonium tetra (pentafluorophenyl) borate, 4-phenylthiophenyldiphenylsulfonium tetrafluoroborate 4-phenylthiophenyldi E sulfonyl sulfonium hexafluorophosphonate, and the like 4-phenylthiophenyldiphenylsulfonium hexafluoroarsenate.

  An example of a trade name of an initiator used for photocationic polymerization is DTS-102 of Midori Chemical Co., Ltd. Examples of this are U.S.C. Syracure UVI-6990, Syracure UVI-6974, Syracure UVI-6922, and the like. Examples of this include Adeka optomer SP-150, SP-152, SP-170, SP-172, etc. of Asahi Denka Co., Ltd. Examples are Rhodia's PHOTOINITITOR 2074, Ciba Specialty's Irgacure 250, GE Silicones' UV-9380C, and the like.

  Examples of solvents are benzene, toluene, xylene, mesitylene, n-butylbenzene, diethylbenzene, tetralin, methoxybenzene, 1,2-dimethoxybenzene, ethylene glycol dimethyl ether, diethylene glycol dimethyl ether, acetone, methyl ethyl ketone, methyl isobutyl ketone, cyclopentanone. , Cyclohexanone, ethyl acetate, ethyl lactate, ethylene glycol monomethyl ether acetate, propylene glycol monomethyl ether acetate, propylene glycol monoethyl ether acetate, γ-butyrolactone, 2-pyrrolidone, N-methyl-2-pyrrolidone, dimethylformamide, chloroform, dichloromethane , Carbon tetrachloride, dichloroethane, tetrachloroethylene, trichloroethylene Emissions, tetrachlorethylene, chlorobenzene, t- butyl alcohol, diacetone alcohol, glycerin, monoacetin, ethylene glycol, triethylene glycol, hexylene glycol, ethylene glycol monomethyl ether, ethyl cellosolve, and the like butyl cellosolve. The solvent may be a single compound or a mixture.

  Next, the polymer will be described. Compound (1) has a polymerizable group. A polymer is obtained by polymerizing a composition containing these compounds. The obtained polymer has optical anisotropy. The kind of reaction is anionic polymerization, cationic polymerization, coordination polymerization, living polymerization and the like. Considering the nature of the polymerizable group, the preferred reaction is cationic polymerization. When obtaining a polymer with excellent orientation, cationic polymerization by irradiation with light is more preferred. This is because it is easy to perform polymerization under the condition that the composition is liquid crystal.

Preferred types of light are ultraviolet light, visible light, infrared light, and the like. Electromagnetic waves such as electron beams and X-rays may be used. Usually, ultraviolet rays or visible rays are preferable. A preferable wavelength range is 150 to 500 nm. A more preferable range is 250 to 450 nm, and a most preferable range is 300 to 400 nm. The light source is a low-pressure mercury lamp (sterilization lamp, fluorescent chemical lamp, black light), high-pressure discharge lamp (high-pressure mercury lamp, metal halide lamp), or short arc discharge lamp (super-high pressure mercury lamp, xenon lamp, mercury xenon lamp). is there. A preferred light source is an ultra high pressure mercury lamp. You may irradiate the composition with the light from a light source as it is. The composition may be irradiated with a specific wavelength (or a specific wavelength region) selected by a filter. A preferable irradiation energy density is ² to 5000 mJ / cm ² . A more preferable range is 10 to 3000 mJ / cm ² . A particularly preferable range is 100 to 2000 mJ / cm ² . A preferable illuminance is 0.1 to 5000 mW / cm ² . Further preferable illuminance is 1 to 2000 mW / cm ² . The temperature at which light is irradiated is set so that the composition has a liquid crystal phase. A preferable irradiation temperature is 100 ° C. or less. Since polymerization by heat can occur at a temperature of 100 ° C. or higher, there are cases where good orientation cannot be obtained.

  When polymerizing composition A, a homopolymer is obtained. This homopolymer consists of one structural unit. When composition B or composition C is polymerized, a copolymer is obtained. This copolymer has at least two structural units. The arrangement of the structural units in the copolymer may be random, block, alternating, or the like. When the composition D is polymerized, a polymer containing a non-polymerizable compound inhomogeneously is obtained. The polymer has at least one structural unit.

  A thermosetting resin can be synthesized by using the compound (1) as a monomer. Since this resin has a three-dimensional crosslinked structure, it does not dissolve in a solvent and does not melt. Therefore, the molecular weight cannot be measured. When synthesizing the thermosetting resin, preferred second components in the copolymerization are compounds (M1) to (M4).

  The shape of the polymer is a film, a plate or the like. The polymer may be molded. In order to obtain a film polymer, a support substrate is generally used. A film is obtained by applying the composition on a support substrate and polymerizing a paint film having a liquid crystal phase. The preferred polymer thickness depends on the value of the optical anisotropy of the polymer and the application. Therefore, although the range cannot be determined strictly, the preferable thickness is in the range of 0.05 to 50 μm, and the more preferable thickness is in the range of 0.1 to 20 μm. A particularly preferred thickness is in the range of 0.5 to 10 μm. The haze value (haze value) of these polymers is generally 1.5% or less. The transmittance of these polymers is generally 80% or more in the visible light region. Therefore, these polymers are suitable as optically anisotropic thin films used for liquid crystal display elements.

  Examples of the support substrate are triacetyl cellulose, polyvinyl alcohol, polyimide, polyester, polyarylate, polyetherimide, polyethylene terephthalate, polyethylene naphthalate, and the like. Examples of product names include “Arton” from JSR Corporation, “Zeonex” and “Zeonoa” from Nippon Zeon Corporation, “Apel” from Mitsui Chemicals, Inc., and the like. The support substrate is a uniaxially stretched film, a biaxially stretched film, or the like. A preferred support substrate is a triacetyl cellulose (TAC) film or “Zeonor”. You may use this film as it is, without pre-processing. This film may be subjected to a surface treatment such as a saponification treatment, a corona discharge treatment, or a UV-ozone treatment as necessary. Other examples include a support substrate made of metal such as aluminum, iron and copper, and a support substrate made of glass such as alkali glass, borosilicate glass and flint glass.

  The coating film on the support substrate is prepared by applying the composition as it is. The coating film can also be prepared by dissolving the composition in a suitable solvent and applying it, and then removing the solvent. Examples of the coating method include spin coating, roll coating, caten coating, flow coating, printing, micro gravure coating, gravure coating, wire bar coating, dip coating, spray coating, meniscus coating, and cast film formation.

  Factors that determine the alignment of the liquid crystal composition are 1) the chemical structure of the polymerizable compound, 2) the type of the supporting substrate, 3) the method of alignment treatment, and the like. The item 1) depends on the type of the side chain, ring, bonding group, polymerizable group and the like of the polymerizable compound. Regarding item 2), it depends on the material of the support substrate such as polymer, glass, metal and the like. Regarding item 3), there are methods such as rubbing in one direction with a rayon cloth or the like (rubbing), oblique deposition of silicon oxide, or etching into a slit shape. In the rubbing process, the support substrate may be directly rubbed. The support substrate may be coated with a thin film such as polyimide or polyvinyl alcohol, and the thin film may be rubbed. Special thin films that give good orientation without rubbing are also known.

  Classification according to the alignment state of liquid crystal molecules includes homogenous (parallel), homeotropic (vertical), hybrid, tilt, twist, and the like. Homogeneous means a state in which the orientation vector is parallel to the substrate and in one direction. Homeotropic means a state in which the orientation vector is perpendicular to the substrate. Hybrid refers to a state in which the orientation vector rises from parallel to vertical as the distance from the substrate increases. Tilt refers to a state in which the orientation vector is rising with a constant tilt angle with respect to the substrate. These orientations are observed in a composition having a nematic phase or the like. On the other hand, twist orientation is observed in a composition having a chiral nematic phase, a cholesteric phase, or the like. The twist refers to a state in which the orientation vector is parallel to the substrate but gradually twists as the distance from the substrate increases. This twist is caused by the action of an optically active group.

  The use of the polymer will be described. This polymer can be used as a molded product having optical anisotropy. The element containing this polymer is an optical film such as a retardation plate (a half-wave plate, a quarter-wave plate, etc.), an antireflection film, a selective reflection film, and a viewing angle compensation film. Polymers having orientation such as homogeneous, hybrid, and homeotropic can be used for retardation plates, polarizing elements, liquid crystal alignment films, antireflection films, selective reflection films, viewing angle compensation films, and the like. Polymers having an orientation such as twist can be used for retardation plates, polarizing elements, selective reflection films, viewing angle compensation films, and the like. Such a polymer is used for the purpose of optical compensation in a retardation plate of a liquid crystal display, a viewing angle compensation film, and the like. Such a polymer can also be used for highly heat-conductive epoxy resins, adhesives, synthetic polymers having mechanical anisotropy, cosmetics, decorations, nonlinear optical materials, information storage materials, and the like.

  The thermosetting resin is suitable for uses such as a retardation plate, a polarizing element, a liquid crystal alignment film, an antireflection film, a selective reflection film, and a viewing angle compensation film, which are constituent elements of a liquid crystal display element.

  The retardation plate has a function of converting the polarization state. The half-wave function plate has a function of rotating the vibration direction of linearly polarized light by 90 degrees. The composition is applied onto the support substrate so as to satisfy the formula d = λ / 2 × Δn. Here, d is the thickness of the composition, λ is the wavelength, and Δn is the optical anisotropy. After the composition is oriented, it is photopolymerized to obtain a half-wavelength functional plate. On the other hand, the 1/4 wavelength functional plate has a function of converting linearly polarized light into circularly polarized light or converting circularly polarized light into linearly polarized light. In this case, a coating film of the composition may be prepared so as to satisfy the condition of d = λ / 4 × Δn. The thickness (d) of the polymer is adjusted as follows. In the method of applying the composition on a support substrate after diluting the composition with a solvent, a coating film having a desired thickness can be obtained by appropriately selecting the concentration of the composition, the application method, the application conditions, and the like. Can do. A method using a liquid crystal cell is also preferable. The liquid crystal cell is convenient because it has an alignment film such as polyimide. When injecting the composition into the liquid crystal cell, the thickness of the coating film can be adjusted by the interval of the liquid crystal cell.

  A polymer having a twist orientation is useful as a retardation plate. When the pitch of the helix is 1 / n of the wavelength (n is the average refractive index of the polymer), light of this wavelength is reflected according to Bragg's law and converted to circularly polarized light. The direction of circularly polarized light depends on the direction of the helix, that is, the configuration of the optically active compound. The direction of circularly polarized light can be determined by appropriately selecting the configuration of the optical compound. This polymer is useful as a circularly polarized light separating functional element.

  This polymer is also useful as a brightness enhancement film. For example, according to the method disclosed in JP-A-6-281814, a polymer in which the helical pitch continuously extends in the thickness direction can be obtained. This polymer can reflect light in a wide wavelength range corresponding to the pitch. This polymer can selectively reflect light in a region of 100 to 350 nm (or a wavelength of 350 to 750 nm).

  After describing the measurement methods of physical properties, the present invention will be described in detail by examples. The example is an example of the present invention. The present invention is not limited by the following examples. The proportion of the composition is wt% (wt%).

  The phase transition temperature was raised at a rate of 1 ° C./min by placing a sample on a hot plate of a melting point measurement apparatus equipped with a polarizing microscope. The temperature at which the liquid crystal phase transitions was measured. C is a crystal, N is a nematic phase, Ch is a cholesteric phase, SmA is a smectic A phase, and I is an isotropic liquid. The NI point is the upper limit temperature of the nematic phase or the transition temperature from the nematic phase to the isotropic liquid. “C50N63I” indicates that the crystal transitioned to the nematic phase at 50 ° C., and the transition from the nematic phase to the isotropic liquid at 63 ° C.

  The cellotape (registered trademark) peel test was in accordance with the test method of JIS standard “JIS-K-5400, 8.5, adhesion (8.5.2, cross-cut tape method)”. That is, the result was evaluated by the number of squares that did not peel out of 100 squares.

  Pencil hardness followed the method of JIS standard "JIS-K-5400, 8.4, pencil scratch test". The result was expressed by the hardness of the pencil lead.

  The heat resistance test was performed at 100 ° C. for 500 hours, and the result was evaluated by the variation of retardation. A polyamic acid (PIA5310 from Chisso Corporation) was applied to the glass substrate, and then heated at 210 ° C. for 30 minutes to obtain a support substrate. The surface of the polyimide produced by heating was rubbed with a rayon cloth. The composition of the sample was diluted with a mixed solvent of toluene and cyclopentanone (2: 1 by weight) to prepare a 30% by weight solution. The solution was applied to a support substrate with a spin coater, heated at 70 ° C. for 3 minutes, and then the produced coating film was irradiated with ultraviolet rays at 60 ° C. for 10 seconds using an ultrahigh pressure mercury lamp (250 W / cm). The retardation of the obtained polymer was measured at 25 ° C. After heating the polymer at 100 ° C. for 500 hours, the retardation was measured again at 25 ° C. Two values were compared to evaluate heat resistance. Retardation was measured using a Senarmont compensator according to literature methods. The wavelength used is 550 nm. Literature is written by Hiroshi Ashiya, “Introduction to Polarizing Microscopes of Polymer Materials”, p. 94, published by Agne Technology Center, 2001.

  The optical anisotropy (Δn) was calculated as follows. The value of retardation (25 ° C.) of the polymer was measured according to the method of heat resistance test. The thickness (d) of the polymer was also measured. Since retardation is Δn × d, the value of optical anisotropy was calculated from this relationship.

  The orientation was observed with a polarizing microscope. The polymer was prepared on a saponified TAC film (support substrate). This sample was sandwiched between two polarizing plates arranged in crossed Nicols. The type of orientation was judged from the angle dependency of transmitted light intensity.

Example 1
First Stage Preparation of 4- [6- (3-Methyloxetane-3-ylmethoxy) hexyloxy] benzoate 3-[(6-Bromohexyloxy) methyl] -3-methyloxetane 84 g, 4-hydroxybenzoic acid A reaction mixture consisting of 50 g of ethyl, 50 g of potassium carbonate and 600 ml of dimethylformamide was stirred at 90 ° C. for 4 hours. Water was added to the reaction mixture to terminate the reaction, extraction was performed with ethyl acetate, the organic layer was washed with a 2N sodium hydroxide aqueous solution and water in this order, and the organic layer was dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel chromatography (toluene / ethyl acetate = 8/2), and 85 g of 4- [6- (3-methyloxetan-3-ylmethoxy) hexyloxy] benzoate Ethyl acid was obtained.

Second Step Preparation of 4- [6- (3-Methyloxetane-3-ylmethoxy) hexyloxy] benzoic acid 83 g of ethyl 4- [6- (3-methyloxetane-3-ylmethoxy) hexyloxy] benzoate, hydroxylated A reaction mixture consisting of 12 g sodium, 50 ml water and 200 ml Solmix® was refluxed for 2 hours. The mixture was acidified with hydrochloric acid, extracted with ethyl acetate, and the organic layer was dried over anhydrous magnesium sulfate. The solvent was distilled off to obtain 63 g of 4- [6- (3-methyloxetan-3-ylmethoxy) hexyloxy] benzoic acid (OX1). Melting point: 58.5 ° C

The following compounds were produced by the same production method.
4- [6- (3-Ethyloxetane-3-ylmethoxy) hexyloxy] benzoic acid (OX2) (melting point: 61 ° C.)

4- [4- (3-Ethyloxetane-3-ylmethoxy) butyloxy] benzoic acid (OX3) (melting point: 75.3-77.7 ° C.)

2-Fluoro-4- [4- (3-ethyloxetane-3-ylmethoxy) butyloxy] benzoic acid (OX4) (melting point: 75-80 ° C.)

Preparation of 4- (3-methyloxetane-3-ylmethoxy) benzoic acid 1st stage 3-ethyl 3-hydroxymethyl-oxetane (manufactured by Toa Gosei Co., Ltd .: trade name OXT-101) was added to 500 ml of pyridine and stirred. While cooling to 0 ° C. Thereto, 190 g of p-toluenesulfonyl chloride was added in several portions. After stirring for 5 hours while maintaining 0 ° C., the reaction solution was poured into 1 L of ice water. Extraction was performed with 500 ml of diethyl ether, and the diethyl ether layer was washed with 3% hydrochloric acid until the pH became acidic, then washed successively with saturated sodium carbonate solution and water, and dried over anhydrous magnesium sulfate. The solvent was distilled off to obtain 243 g of 3-[(tosyloxy) methyl] -3-ethyloxetane.

Second stage 50 g of ethyl hydroxybenzoate and 21 g of potassium hydroxide were added to 400 ml of dimethylformamide and stirred at 70 ° C. for 1 hour. The temperature was lowered to 45 ° C., and 100 g of 3-[(tosyloxy) methyl] -3-ethyloxetane was added dropwise thereto, followed by stirring for 3 hours while maintaining the temperature at 45 ° C. Water and toluene were added for extraction, and the toluene layer was washed with 3% hydrochloric acid, saturated sodium bicarbonate and water, and then toluene was distilled off. To the obtained residue, 50 g of sodium hydroxide, 500 ml of ethanol, and 200 ml of water were added and refluxed for 2 hours. When the residue obtained by distilling off ethanol was poured into 500 ml of 5% hydrochloric acid, crystals were obtained. The crystals obtained by filtration were recrystallized with a mixed solvent of ethanol and water to obtain 60 g of 4- (3-ethyloxetane-3-ylmethoxy) benzoic acid (OX5). Melting point: 127.5 ° C.

  19 g of ethyl 4-hydroxycinnamate and 7.3 g of potassium hydroxide were added to 150 ml of ethanol and stirred at 50 ° C. for 1 hour. The temperature was lowered to 40 ° C., and 35 g of 3-[(tosyloxy) methyl] -3-ethyloxetane was added dropwise thereto, followed by refluxing for 3 hours. Ethanol was distilled off, water and toluene were added for extraction, the toluene layer was washed with 3% hydrochloric acid, saturated sodium bicarbonate and water, and then toluene was distilled off. To the obtained residue, 20 g of sodium hydroxide, 100 ml of ethanol and 50 ml of water were added and refluxed for 2 hours. When the residue obtained by distilling off ethanol was poured into 500 ml of 5% hydrochloric acid, crystals were obtained. The crystals obtained by filtration were recrystallized with a mixed solvent of ethanol and water to obtain 5 g of 4- (3-ethyloxetane-3-ylmethoxy) cinnamic acid (OX6). Melting point: 127.5 ° C.

  17.4 g of ethyl 3- (4-hydroxyphenyl) propionate and 6.1 g of potassium hydroxide were added to 150 ml of ethanol and stirred at 60 ° C. for 1 hour. The temperature was lowered to 40 ° C., and 30 g of 3-[(tosyloxy) methyl] -3-ethyloxetane was added dropwise thereto, followed by refluxing for 3 hours. Ethanol was distilled off, water and toluene were added for extraction, the toluene layer was washed with 3% hydrochloric acid, saturated sodium bicarbonate and water, and then toluene was distilled off. To the obtained residue, 20 g of sodium hydroxide, 100 ml of ethanol and 50 ml of water were added and refluxed for 2 hours. When the residue obtained by distilling off ethanol was poured into 500 ml of 5% hydrochloric acid, crystals were obtained. The crystals obtained by filtration were recrystallized with a mixed solvent of ethanol and water to obtain 5 g of [4- (3-ethyloxetane-3-ylmethoxy) phenyl] propionic acid (OX7). Melting point: 85 ° C.

Synthesis of 4,4′-dihydroxy-3,3′-dimethylbiphenyl (first stage)
To a solution obtained by dissolving 40.4 g of 3,3′-dimethylbiphenyl in 200 ml of carbon disulfide, 127.1 g of aluminum chloride was added. The mixture was cooled to 5 ° C. using an ice bath, acetyl chloride 38.1 was added dropwise thereto, and the mixture was stirred at room temperature for 1 day. The reaction solution was poured into ice water to complete the reaction. Ethyl acetate was added for extraction, and the organic layer was washed with 6N hydrochloric acid, saturated aqueous sodium carbonate and water, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the resulting residue was recrystallized from ethanol to obtain 16 g of 4,4′-diacetyl-3,3′-dimethylbiphenyl. The melting point was 130-131 ° C.

(Second stage)
19.3 g of 4,4′-diacetyl-3,3′-dimethylbiphenyl, 74.4 g of formic acid and 28.3 g of acetic anhydride were added to 240 ml of methylene chloride. To the solution cooled in an ice bath, 8.2 ml of sulfuric acid and then 32.5 g of hydrogen peroxide were dropped, and the mixture was refluxed for 5 hours. Water was added for extraction, and the methylene chloride layer was washed with a 2N aqueous sodium hydroxide solution and a 10% aqueous sodium bisulfite solution. Methylene chloride was removed by distillation under reduced pressure, and the resulting residue was recrystallized from ethanol to obtain 12.5 g of 4,4′-diacetoxy-3,3′-dimethylbiphenyl. The melting point was 124-134 ° C.

(3rd stage)
1,4 g of 4,4′-diacetoxy-3,3′-dimethylbiphenyl and 4.4 g of lithium hydroxide were added to 130 ml of ethylene glycol and refluxed for 3 hours. The reaction solution was poured into 200 ml of 6N hydrochloric acid and extracted with ethyl acetate. The ethyl acetate layer was separated and the solvent was distilled off. The obtained residue was recrystallized from chloroform to obtain 5.5 g of 4,4′-dihydroxy-3,3′-dimethylbiphenyl. The melting point was 154-159 ° C.

  4,4′-dihydroxy-3,3′-dimethylbiphenyl 0.5 g, 4- [4- (3-ethyloxetane-3-ylmethoxy) butyloxy] benzoic acid (OX3) 1.6 g, dimethylaminopyridine 0.1 g Was added to 20 ml of methylene chloride and 1 g of 1-ethyl-3- (3-dimethylaminopropyl) carbodiimide hydrochloride was added and stirred at room temperature for 12 hours. 50 ml of water was added, and the obtained organic layer was dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel chromatography to obtain 0.8 g of Compound No. 15 was obtained. The phase transition temperature was C 105 N 122.8 I.

Example 2

  0.5 g of 4,4′-dihydroxy-3,3′-dimethylbiphenyl, 1.7 g of 4- [4- (3-methyloxetan-3-ylmethoxy) hexyloxy] benzoic acid (OX1), 0.7 g of dimethylaminopyridine. 1 g of 1-ethyl-3- (3-dimethylaminopropyl) carbodiimide hydrochloride was added to a solution of 1 g in 20 ml of methylene chloride, and the mixture was stirred at room temperature for 12 hours. 50 ml of water was added, and the obtained organic layer was dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel chromatography to obtain 0.8 g of Compound No. 31 was obtained. The phase transition temperature was C 95.2 N 135.7 I.

Example 3
(First stage)
4-Bromo-2,6-dimethylphenol 45.5 g benzyl chloride 34.4 g and potassium hydroxide 15.2 g were added to ethanol 400 ml and refluxed for 6 hours. Water was added and the mixture was extracted with ethyl acetate. The extracted solution was washed with 2N aqueous sodium hydroxide and dried over anhydrous magnesium sulfate. The solvent was distilled off to obtain 44 g of 4-benzyloxy-3,5-dimethylbromobenzene.

(Second stage)
A solution of 20 g of 4-benzyloxy-3,5-dimethylbromobenzene dissolved in 50 ml of tetrahydrofuran was added to the extent that 1.8 g of magnesium was immersed and heated. After confirming that magnesium was dissolved and reacted, the remaining solution was added dropwise. After completion of the dropwise addition, the mixture was refluxed for 1 hour to prepare a Grignard reagent. The Grignard reagent solution was cooled to −8 ° C., and 9.9 g of trimethyl borate was added dropwise thereto and stirred for 30 minutes. 50 ml of 6N hydrochloric acid was added and extracted with ethyl acetate. The ethyl acetate layer was washed with water, saturated aqueous sodium carbonate, and water in this order. The residue obtained by distilling off the solvent was recrystallized from toluene to obtain 9.4 g of 4-benzyloxy-3,5-dimethylbenzeneboronic acid.

（第３段階）
４−ベンジルオキシ−３、５−ジメチルベンゼンホウ素酸９．４ｇ、４−ベンジルオキシブロモベンゼン９．５ｇ、テトラキスパラジウム１．２ｇ、炭酸ナトリウム２Ｍ水溶液３６ｍｌをジエチレングリコールジメチルエーテル９０ｍｌに加え６時間還流した。水を加え酢酸エチルで抽出、無水硫酸マグネシウムで乾燥した。溶媒を留去して得られた残査をアセトンで再結晶して８．９ｇの４，４'−ジベンジルオキシ−３，５−ジメチルビフェニルを得た。

(3rd stage)
9.4 g of 4-benzyloxy-3,5-dimethylbenzeneboronic acid, 9.5 g of 4-benzyloxybromobenzene, 1.2 g of tetrakis palladium, and 36 ml of 2M aqueous sodium carbonate solution were added to 90 ml of diethylene glycol dimethyl ether and refluxed for 6 hours. Water was added, extracted with ethyl acetate, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was recrystallized from acetone to obtain 8.9 g of 4,4′-dibenzyloxy-3,5-dimethylbiphenyl.

(3rd stage)
Hydrogen was introduced at normal pressure into a flask in which 8.9 g of 4,4′-dibenzyloxy-3,5-dimethylbiphenyl and 0.4 g of palladium carbon were added to 100 ml of tetrahydrofuran, and stirred until hydrogen was not absorbed. The catalyst was removed by filtration, and the solvent was distilled off to obtain 4.3 g of 4,4′-dihydroxy-3,5-dimethylbiphenyl. The melting point was 160.7-166 ° C.

  4,4′-dihydroxy-3,5-dimethylbiphenyl 0.5 g, 4- [4- (3-methyloxetane-3-ylmethoxy) hexyloxy] benzoic acid (OX1) 1.65 g, dimethylaminopyridine 0.05 g Was added to 20 ml of methylene chloride and 1 g of 1-ethyl-3- (3-dimethylaminopropyl) carbodiimide hydrochloride was added and stirred at room temperature for 12 hours. 50 ml of water was added, and the obtained organic layer was dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel chromatography, and 0.5 g of Compound No. 30 was obtained. The phase transition temperature was C 85.6 N 129 I.

Example 4
(First stage)
A solution prepared by dissolving 20 g of 4-benzyloxy-3-fluorobromobenzene in 100 ml of tetrahydrofuran was added to the extent that 1.9 g of magnesium was immersed and heated. After confirming that magnesium was dissolved and reacted, the remaining solution was added dropwise. After completion of the dropwise addition, the mixture was refluxed for 1 hour to prepare a Grignard reagent. The Grignard reagent solution was cooled to −8 ° C., and 10.2 g of trimethyl borate was added dropwise thereto and stirred for 30 minutes. 50 ml of 6N hydrochloric acid was added and extracted with ethyl acetate. The ethyl acetate layer was washed with water, saturated aqueous sodium carbonate, and water in this order. The residue obtained by distilling off the solvent was recrystallized from toluene to obtain 10.3 g of 4-benzyloxy-3-fluorobenzeneboronic acid.

(Second stage)
4-benzyloxy-3-fluorobenzeneboronic acid 5 g, 4-benzyloxy-3,5-dimethylbromobenzene 5.8 g, tetrakis palladium 0.7 g, 20 ml of a 2 M sodium carbonate solution were added to 50 ml of diethylene glycol dimethyl ether and refluxed for 6 hours. . Water was added, extracted with ethyl acetate, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was recrystallized from acetone to obtain 7 g of 4,4′-dibenzyloxy-3,5-dimethyl-3′-fluorobiphenyl.

(3rd stage)
Hydrogen was introduced at normal pressure into a flask in which 7 g of 4,4′-dibenzyloxy-3,5-dimethyl-3′-fluorobiphenyl and 0.3 g of palladium carbon were added to 100 ml of tetrahydrofuran, and stirred until hydrogen was not absorbed. did. The catalyst was removed by filtration, and the solvent was distilled off to obtain 4 g of 4,4′-dihydroxy-3,5-dimethyl-3′-fluorobiphenyl. The melting point was 158-160.6 ° C.

  4,4′-dihydroxy-3,5-dimethyl-3′-fluorobiphenyl 0.5 g, 4- [4- (3-methyloxetan-3-ylmethoxy) hexyloxy] benzoic acid (OX1) 1.5 g, dimethyl To a solution obtained by adding 0.1 g of aminopyridine to 20 ml of methylene chloride, 0.95 g of 1-ethyl-3- (3-dimethylaminopropyl) carbodiimide hydrochloride was added and stirred at room temperature for 12 hours. 50 ml of water was added, and the obtained organic layer was dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel chromatography to obtain 0.8 g of Compound No. 32 was obtained. The phase transition temperature was C94N100I.

Example 5
(First stage)
A solution prepared by dissolving 27 g of 4-benzyloxy-2,5-dimethylbromobenzene in 70 ml of tetrahydrofuran was added to the extent that 2.3 g of magnesium was immersed and heated. After confirming that magnesium was dissolved and reacted, the remaining solution was added dropwise. After completion of the dropwise addition, the mixture was refluxed for 1 hour to prepare a Grignard reagent. The Grignard reagent solution was cooled to −8 ° C., and 13.4 g of trimethyl borate was added dropwise thereto and stirred for 30 minutes. 50 ml of 6N hydrochloric acid was added and extracted with ethyl acetate. The ethyl acetate layer was washed with water, saturated aqueous sodium carbonate, and water in this order. The solvent was distilled off to obtain 13.9 g of 4-benzyloxy-2,5-dimethylbenzeneboronic acid.

(Second stage)
9 g of 4-benzyloxy-2,5-dimethylbenzeneboronic acid, 9.5 g of 4-benzyloxybromobenzene, 1.2 g of tetrakis palladium, and 36 ml of a 2M sodium carbonate solution were added to 90 ml of diethylene glycol dimethyl ether and refluxed for 6 hours. Water was added, extracted with ethyl acetate, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was recrystallized from acetone to obtain 7.1 g of 4,4′-dibenzyloxy-2,5-dimethylbiphenyl.

(3rd stage)
Hydrogen was introduced at normal pressure into a flask in which 7.1 g of 4,4′-dibenzyloxy-2,5-dimethylbiphenyl and 0.4 g of palladium carbon were added to 100 ml of tetrahydrofuran, and stirred until hydrogen was not absorbed. The catalyst was removed by filtration, and the solvent was distilled off to obtain 5 g of 4,4′-dihydroxy-2,5-dimethylbiphenyl.

  4,4′-dihydroxy-2,5-dimethylbiphenyl 0.5 g, 4- [4- (3-methyloxetane-3-ylmethoxy) hexyloxy] benzoic acid (OX1) 1.65 g, dimethylaminopyridine 0.05 g Was added to 20 ml of methylene chloride and 1 g of 1-ethyl-3- (3-dimethylaminopropyl) carbodiimide hydrochloride was added and stirred at room temperature for 12 hours. 50 ml of water was added, and the obtained organic layer was dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel chromatography, and 0.7 g of Compound No. 29 was obtained.

Example 6

(First stage)
10 g of 4-benzyloxy-3-fluorobenzeneboronic acid, 5 g of 1,4-dibromo-3-methylbenzene, 0.2 g of tetrakis palladium, and 60 ml of a sodium carbonate 2M solution were added to 100 ml of diethylene glycol dimethyl ether and refluxed for 6 hours. When water was added, crystals were precipitated, and filtered to dry the crystals. Recrystallization from acetone gave 8.4 g of compound [TB1].

(Second stage)
Compound [TB1] 8.4 g palladium carbon 0.6 was added to 100 ml of tetrahydrofuran, hydrogen was introduced at normal pressure, and the mixture was stirred until hydrogen was not absorbed. The catalyst was removed by filtration, and the solvent was distilled off to obtain 6 g of compound [TF1].

(3rd stage)
To a solution obtained by adding 0.3 g of compound [TF1], 1.68 g of 4- [4- (3-methyloxetane-3-ylmethoxy) hexyloxy] benzoic acid (OX1) and 0.005 g of dimethylaminopyridine to 20 ml of methylene chloride. 0.42 g of 1-ethyl-3- (3-dimethylaminopropyl) carbodiimide hydrochloride was added, and the mixture was stirred at room temperature for 12 hours. 50 ml of water was added, and the obtained organic layer was dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel chromatography, and 0.5 g of Compound No. 28 was obtained. The phase transition temperature was C 109.2 N 229.4 I.

Example 7
To a solution of 0.3 g of compound [TF1], 1.65 g of 4- [4- (3-ethyloxetane-3-ylmethoxy) butyloxy] benzoic acid (OX3) and 0.005 g of dimethylaminopyridine was added to 20 ml of methylene chloride. -Ethyl-3- (3-dimethylaminopropyl) carbodiimide hydrochloride 0.42g was added, and it stirred at room temperature for 12 hours. 50 ml of water was added, and the obtained organic layer was dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel chromatography, and 0.2 g of Compound No. 12 was obtained. The phase transition temperature was C 91 N 225.2 I.

Example 8
(First stage)
10 g of 4-benzyloxy-3-fluorobenzeneboronic acid, 4.8 g of 1,4-dibromobenzene, 0.2 g of tetrakis palladium, and 60 ml of a 2M sodium carbonate solution were added to 100 ml of diethylene glycol dimethyl ether and refluxed for 6 hours. When water was added, crystals were precipitated, and filtered to dry the crystals. Recrystallization from acetone gave 4.7 g of compound [TB2].

(Second stage)
Hydrogen was introduced at normal pressure into a flask in which 4.7 g of compound [TB2] and 0.5 g of palladium carbon were added to 40 ml of tetrahydrofuran, and the mixture was stirred until hydrogen was not absorbed. The catalyst was removed by filtration, and the solvent was distilled off to obtain 2.9 g of compound [TF2].

  To a solution of 0.3 g of compound [TF2], 0.7 g of 4- [4- (3-ethyloxetane-3-ylmethoxy) butyloxy] benzoic acid (OX4) and 0.05 g of dimethylaminopyridine was added to 20 ml of methylene chloride. -Ethyl-3- (3-dimethylaminopropyl) carbodiimide hydrochloride 0.5g was added, and it stirred at room temperature for 12 hours. 50 ml of water was added, and the obtained organic layer was dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel chromatography, and 0.4 g of Compound No. 10 was obtained. The phase transition temperature was C 128 SmA 205.2 N 298.3 I.

Example 9
(First stage)
10 g of 4-benzyloxy-3-fluorobenzeneboronic acid, 5.1 g of 1,4-dibromo-2-fluorobenzene, 0.2 g of tetrakis palladium, and 60 ml of a 2 M sodium carbonate solution were added to 100 ml of diethylene glycol dimethyl ether and refluxed for 6 hours. When water was added, crystals were precipitated, and filtered to dry the crystals. Recrystallization from acetone gave 5.9 g of compound [TB3]. The melting point was 189-192.1 ° C.

(Second stage)
Hydrogen was introduced at normal pressure into a flask in which 5.7 g of compound [TB3] and 0.5 g of palladium carbon were added to 40 ml of tetrahydrofuran, and stirred until hydrogen was not absorbed. The catalyst was removed by filtration, and the solvent was distilled off to obtain 3.4 g of compound [TF3].

To a solution of 0.32 g of compound [TF3], 0.7 g of 4- [4- (3-ethyloxetane-3-ylmethoxy) butyloxy] benzoic acid (OX3) and 0.05 g of dimethylaminopyridine was added to 20 ml of methylene chloride. -Ethyl-3- (3-dimethylaminopropyl) carbodiimide hydrochloride 0.5g was added, and it stirred at room temperature for 12 hours. 50 ml of water was added, and the obtained organic layer was dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel chromatography, and 0.5 g of Compound No. 11 was obtained. The phase transition temperature was 109.5 SmA 163.5 N 278.6 I.

Example 10
(First stage)
4-benzyloxy-3,5-dimethylbenzeneboronic acid 5g, 4-bromo-4'-benzyloxybiphenyl 6.6g, tetrakis palladium 0.6g, sodium carbonate 2M solution 19ml was added to diethylene glycol dimethyl ether 100ml and refluxed for 6 hours. . When water was added, crystals were precipitated, and filtered to dry the crystals. Recrystallization from acetone gave 7 g of compound [TB4].

(Second stage)
Hydrogen was introduced at normal pressure into a flask in which 7 g of compound [TB4] and 0.5 g of palladium carbon were added to 40 ml of tetrahydrofuran, and stirred until hydrogen was not absorbed. The catalyst was removed by filtration, and the solvent was distilled off to obtain a residue. The residue was purified by silica gel column chromatography using methylene chloride as an elution solvent to obtain 1 g of compound [TF4]. The melting point was 231 ° C.

  To a solution of 0.3 g of compound [TF4], 0.7 g of 4- [4- (3-ethyloxetane-3-ylmethoxy) butyloxy] benzoic acid (OX3) and 0.05 g of dimethylaminopyridine was added to 20 ml of methylene chloride. -Ethyl-3- (3-dimethylaminopropyl) carbodiimide hydrochloride 0.5g was added, and it stirred at room temperature for 12 hours. 50 ml of water was added, and the obtained organic layer was dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel chromatography to obtain 0.8 g of Compound No. 9 was obtained. The phase transition temperature was C 116 N 250.2 I.

Example 11
(Example of composition C2)
Compound No. 50 wt% Composition (CL1) was prepared from 11 and 50 wt% of compound (K1). Here, the compound (K1) is a compound in which W ¹ and W ² are hydrogen, X ⁶ is a single bond, and m = n = 1 in the formula (M2a), Macromolecules, 26, 1244 to It was synthesized by the method described on page 1249, 1993. This composition had a nematic phase at room temperature. Compound No. 11 had good compatibility and did not phase separate. When the composition (CL1) was applied on a rubbed TAC film, it showed homogeneous orientation.

  After saponifying the TAC film, the surface was rubbed with a rayon cloth. A cyclopentanone (8 g) solution of 1 g of the composition (CL1) and 0.03 g of DTS-102 (polymerization initiator of Midori Chemical Co., Ltd.) was applied to this film using a spin coater. After the application, it was heated in an oven set at 60 ° C. for 5 minutes. The solvent was removed by this heat treatment to align the liquid crystal molecules. An ultra-high pressure mercury lamp (250 W / cm) was used to irradiate ultraviolet rays at 60 ° C. for 10 seconds to obtain a liquid crystal alignment film (F1). The homogeneous orientation of the composition was maintained by polymerization. In the cellotape (registered trademark) peel test of this film, there was no flaking. The pencil hardness of this film was 2H.

Example 12
(Example of composition C1)
Compound No. 70 wt% Composition (CL2) was prepared from 15 and 30 wt% compound (K2). Here, the compound (K2) is a compound in which W ¹ and W ² are hydrogen, X ⁶ is —O—, R ⁵ is —OCF ₃ and m = 4 in the formula (M1a), It was synthesized by the method described in Japanese Patent Application No. 2004-305799. This composition had a nematic phase at room temperature. Compound No. 15 had good compatibility and did not phase separate. Composition (CL2) exhibited hybrid orientation when applied on a rubbed TAC film.

  After saponifying the TAC film, the surface was rubbed with a rayon cloth. A cyclopentanone (8 g) solution of 1 g of the composition (CL2) and 0.03 g of DTS-102 (Midori Chemical Co., Ltd. polymerization initiator) was applied to this film using a spin coater. After the application, it was heated in an oven set at 60 ° C. for 5 minutes. The solvent was removed by this heat treatment to align the liquid crystal molecules. An ultra-high pressure mercury lamp (250 W / cm) was used for irradiation with ultraviolet rays at 60 ° C. for 10 seconds to obtain a liquid crystal alignment film (F2). The hybrid orientation of the composition was retained by polymerization. In the cellotape (registered trademark) peel test of this film, there was no flaking. The pencil hardness of this film was 2H.

The evaluation results of these films are summarized in Table 2. From these results, it was found that 1) the polymer was difficult to peel from the support substrate, and 2) the polymer was hard.
Table 2. Evaluation results

Example 13
(Example of composition C3)
The liquid crystal alignment film (F3) obtained by the method similar to Example 12 using the following composition (CL3) has the same characteristic as the liquid crystal alignment film (F2) of Example 12. Here, in the compound (K3), in formula (M2e), W ¹ and W ² are hydrogen, W ³ is methyl, W ⁴ is hydrogen, m = 4, n = 4, and X = O It is a compound and can be synthesized by the method described in Japanese Patent Application No. 2003-203629.
Composition (CL3)

（組成物Ｃ５の例）
組成物（ＣＬ５）

Example 14
The liquid crystal alignment films (F4) and (F5) obtained by the same method as in Example 11 using the following compositions (CL4) and (CL5) have the same characteristics as the liquid crystal alignment film (F1) in Example 11. Have Here, the compound (K4) is a compound in which W ¹ and W ² are hydrogen, R ⁵ is cyano, R ⁶ is methyl, and m = 4 in the formula (M3e). Macromolecules, 24, pages 4531-4537, 1991 It can be synthesized by the method described in the year. The compound (K5) is a compound in which W ¹ and W ² are hydrogen, W3 is methyl, W4 is hydrogen, R6 is methyl, and m = n = 6 in the formula (M4b), according to the method described in WO02 / 28985 Can be synthesized.

(Example of composition C4)
Composition (CL4)

(Example of composition C5)
Composition (CL5)

Claims (20)

The compound represented by Formula (1).

In the formula (1), R is hydrogen or alkyl having 1 to 8 carbon atoms, and in this alkyl, arbitrary hydrogen may be replaced by fluorine or chlorine; A is independently 1,4-cyclohexylene, 1,4-phenylene, pyridine-2,5-diyl, pyridazine-3,6-diyl, pyrimidine-2,5-diyl, naphthalene-2,6-diyl, or tetrahydronaphthalene-2,6-diyl; In this 1,4-phenylene, any hydrogen may be replaced by fluorine or chlorine, and any one or two hydrogens may be cyano, methyl, ethyl, methoxy, hydroxy, formyl, acetoxy, acetyl, trifluoroacetyl. , Difluoromethyl, or trifluoromethyl; G is at least one hydrogen chloride 4,4 "-terphenyl or at least one hydrogen substituted with fluorine, methyl, ethyl, isopropyl, methoxy, hydroxy, formyl, acetoxy, acetyl, trifluoroacetyl, difluoromethyl, or trifluoromethyl is chlorine, fluorine, 4,4′-biphenyl substituted with methyl, ethyl, isopropyl, methoxy, hydroxy, formyl, acetoxy, acetyl, trifluoroacetyl, difluoromethyl, or trifluoromethyl; Z is independently a single bond, — (CH ₂ ) ₂ , —CH═CH—, —C≡C—, —CH ₂ O—, —OCH ₂ —, —CF ₂ O—, —OCF ₂ —, —COO—, —OCO—, —CONH—, _{-NHCO -, - (CH 2)} 4 -, - (CH 2) 2 COO -, - OCO (CH 2) 2 , —CH═CH—COO—, or —OCO—CH═CH—; P is alkylene having 1 to 20 carbons, and in this alkylene, any hydrogen may be replaced by fluorine or chlorine, —CH ₂ — may be replaced with —O—, any one or two —CH ₂ — may be replaced with —COO— or —OCO—, and any one —CH _{2 —.} -May be replaced by -CH = CH- or -C≡C-. In the formula (1), R is hydrogen or alkyl having 1 to 5 carbon atoms, and in this alkyl, arbitrary hydrogen may be replaced by fluorine or chlorine; A is independently 1,4-phenylene; In this 1,4-phenylene, any hydrogen may be replaced with fluorine or chlorine, and any one or two hydrogens may be replaced with methyl, ethyl or trifluoromethyl; G is at least one 4,4 "-terphenyl substituted with chlorine, fluorine, methyl, ethyl, or trifluoromethyl or 4,4 substituted with at least one hydrogen with chlorine, fluorine, methyl, ethyl, or trifluoromethyl '- biphenyl; Z is independently a single _{bond, - (CH 2) 2 -} , - C≡C -, - CH 2 O -, - OCH 2 -, - C _{O -, - OCO -, -} CONH -, - NHCO -, - (CH 2) 4 -, - (CH 2) 2 COO -, - OCO (CH 2) 2 -, - CH = CH-COO-, or -OCO-CH = CH- and is; P is alkylene of 1 to 17 carbon atoms, any in the alkylene -CH ₂ - may be replaced by -O-, any one or two - The compound of claim 1, wherein CH ₂ — may be replaced with —COO— or —OCO—, and any one —CH ₂ — may be replaced with —CH═CH—. In the formula (1), R is hydrogen or alkyl having 1 to 5 carbon atoms, and in this alkyl, arbitrary hydrogen may be replaced by fluorine or chlorine; A is independently 1,4-phenylene; In this 1,4-phenylene, any hydrogen may be replaced with fluorine or chlorine, and any one or two hydrogens may be replaced with methyl, ethyl, or trifluoromethyl; Having

Z is independently a single bond, — (CH ₂ ) ₂ —, —C≡C—, —CH ₂ O—, —OCH ₂ —, —COO—, —OCO—, —CONH—, —NHCO—, — (CH ₂ ) ₄ —, — (CH ₂ ) ₂ COO—, —OCO (CH ₂ ) ₂ —, —CH═CH—COO—, or —OCO—CH═CH—; 17 alkylene, in which any —CH ₂ — may be replaced by —O—, and any one or two —CH ₂ — may be replaced by —COO— or —OCO—. The compound according to claim 1, wherein any one —CH ₂ — may be replaced by —CH═CH—. The compound represented by any one of following formula (2)-(9).

In the above formula, R is alkyl having 1 to 5 carbon atoms; A is independently 1,4-phenylene, 2-fluoro-1,4-phenylene, 2-chloro-1,4-phenylene, 2-methyl. -1,2-trifluoromethyl-1,4-phenylene, 2,3-difluoro-1,4-phenylene, 2,5-difluoro-1,4-phenylene, 2,6-difluoro-1,4-phenylene 2,3,5-trifluoro-1,4-phenylene, or 2,3,5,6-tetrafluoro-1,4-phenylene; Z is independently a single bond, — (CH ₂ ) ₂ —, —C≡C—, —CH ₂ O—, —OCH ₂ —, —COO—, —OCO—, —CONH—, —NHCO—, — (CH ₂ ) ₄ —, — (CH ₂ ) ₂ COO _{-, - OCO (CH 2)} 2 -, - CH = CH-COO Or -OCO-CH = CH- and is,; -, - P is _{-O O- (CH 2) r -} , - (CH 2) r-O -, - (CH 2) r -, - O- ( CH ₂ ) r—O—, or —O— (CH ₂ CH ₂ O) s—, where r is an integer from 1 to 15 and s is an integer from 2 to 5. In formulas (2) to (9), R is methyl or ethyl; A is independently 1,4-phenylene, 2-fluoro-1,4-phenylene, 2-chloro-1,4-phenylene, 2 -Methyl-1,4-phenylene, 2,3-difluoro-1,4-phenylene, 2,5-difluoro-1,4-phenylene, or 2,6-difluoro-1,4-phenylene; Independently —COO—, —OCO—, — (CH ₂ ) ₂ COO—, —OCO (CH ₂ ) ₂ —, —CH═CH—COO— or —OCO—CH═CH—; O- or -O- _(CH 2) r-O- in and, and the compound of claim 4 r is an integer from 2 to 10. In formulas (2) to (9), R is methyl or ethyl; A is independently 1,4-phenylene, 2-fluoro-1,4-phenylene, 2-chloro-1,4-phenylene, 2 -Methyl-1,4-phenylene, 2,3-difluoro-1,4-phenylene, 2,5-difluoro-1,4-phenylene, or 2,6-difluoro-1,4-phenylene; Independently —COO—, —OCO—, — (CH ₂ ) ₂ COO—, or —OCO (CH ₂ ) ₂ —; P is —O— (CH ₂ ) r—O—, and r The compound according to claim 4, wherein is an integer of 2 to 10. In formulas (2) to (9), R is methyl or ethyl; A is independently 1,4-phenylene, 2-fluoro-1,4-phenylene, 2-chloro-1,4-phenylene, or 2-methyl-1,4-phenylene; Z is independently —COO—, —OCO—, — (CH ₂ ) ₂ COO—, or —OCO (CH ₂ ) ₂ —; P is —O - _(CH 2) r-O- in and, and the compound of claim 4 r is an integer from 2 to 10. In formulas (2) to (9), R is methyl; A is independently 1,4-phenylene; Z is independently —COO— or —OCO—; P is —O— ( CH ₂₎ r-O-a and, and the compound of claim 4 r is an integer from 2 to 10. In formulas (2) to (9), R is ethyl; A is independently 1,4-phenylene; Z is independently —COO— or —OCO—; P is —O— ( CH ₂₎ r-O-a and, and the compound of claim 4 r is an integer from 2 to 10. The composition containing the at least 1 compound of any one of Claims 1-9 as a 1st component. The composition according to claim 10, further comprising a polymerizable compound different from the compound according to any one of claims 1 to 9 as a second component. The composition according to claim 10, wherein the second component is at least one compound selected from the group of compounds represented by formula (M1), formula (M2), formula (M3) and formula (M4).

In the formulas (M1) to (M4), Ra is hydrogen, fluorine, chlorine, —CN, —OCF ₃ , alkyl having 1 to 20 carbons, alkoxy having 1 to 20 carbons, or alkoxyalkyl having 2 to 20 carbons. , Alkenyloxy having 2 to 20 carbons, or alkenyloxy having 2 to 20 carbons; Rb is hydrogen or alkyl having 1 to 5 carbons; B is independently 1,4-cyclohexylene or 1, 4-phenylene, in which any hydrogen may be replaced by fluorine, and any one or two hydrogens may be replaced by methyl or trifluoromethyl, and B One is naphthalene-2,6-diyl, fluorene-2,7-diyl, 9-methylfluorene-2,7-diyl, 9-ethylfluorene-2,7-diyl, , 9-dimethylfluorene-2,7-diyl, 9-chlorofluorene-2,7-diyl, or 9,9-difluorofluorene-2,7-diyl; Y is independently a single bond, —COO—, —OCO—, — (CH ₂ ) ₂ —, or —C≡C—; Q is independently a single bond or alkylene having 1 to 20 carbons, and in this alkylene, one or two Two —CH ₂ may be replaced by —O—; and t is 1 or 2. In the formulas (M1) to (M4), Ra is fluorine, chlorine, —CN, —OCF ₃ , alkyl having 1 to 15 carbons, or alkoxy having 2 to 15 carbons; Rb is hydrogen or 1 carbon ~ 2 alkyl; B is independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 2-chloro-1,4-phenylene, 2-methyl- 1,4-phenylene, 2,3-difluoro-1,4-phenylene, 2,5-difluoro-1,4-phenylene, 2,6-difluoro-1,4-phenylene, 9-methylfluorene-2,7 -Diyl, 9,9-dimethylfluorene-2,7-diyl or 9-ethylfluorene-2,7-diyl; Y is independently a single bond, -COO-, -OCO-, or- C≡C- Q is independently a single bond or alkylene having 1 to 10 carbon atoms, in the alkylene one or two -CH 2 _- may be replaced by -O-; and t is 1 or 2 wherein Item 13. The composition according to Item 12. In the formulas (M1) to (M4), Ra is fluorine, chlorine, —OCF ₃ , alkyl having 1 to 10 carbons, or alkoxy having 2 to 10 carbons; Rb is hydrogen or having 1 to 2 carbons B is independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 2-chloro-1,4-phenylene, 2-methyl-1,4 -Phenylene, 2,3-difluoro-1,4-phenylene, 2,5-difluoro-1,4-phenylene, 2,6-difluoro-1,4-phenylene, 9-methylfluorene-2,7-diyl, May be 9,9-dimethylfluorene-2,7-diyl or 9-ethylfluorene-2,7-diyl; Y is independently a single bond, —COO—, —OCO—, or —C≡C; -Is; Q is German A single _{bond, - (CH 2) m -} , - (CH 2) m-O-, or -O- _(CH 2) a m-, m is an integer from 1 to 10; and t is 1 or 2 The composition according to claim 12. The second component is selected from at least one compound selected from the group of compounds represented by formula (M1) and formula (M2), or a group of compounds represented by formula (M3) and formula (M4) The composition according to claim 10 or 11, which is a compound. The composition according to claim 10 or 11, wherein the second component is a compound selected from the group of compounds represented by formula (M1) or formula (M2). The polymer obtained by polymerizing the compound of any one of Claims 1-9. The polymer obtained by superposing | polymerizing the composition of any one of Claims 10-16. The polymer obtained by orientating the compound of any one of Claims 1-9 or the composition of any one of Claims 10-16, and superposing | polymerizing, maintaining orientation. The film obtained by orientating the compound of any one of Claims 1-9 or the composition of any one of Claims 10-16, and superposing | polymerizing, maintaining orientation.