Polymerizable liquid crystal compound, method for producing polymerizable liquid crystal compound, polymerizable liquid crystal composition, optically anisotropic film, optical film, polarizing plate, and image display device

Patent metadata

Field	Value
Publication number	US-11225605-B2
Application number	US-201916529163-A
Country	US
Kind code	B2
Filing date	Aug 1, 2019
Priority date	Feb 21, 2017
Publication date	Jan 18, 2022
Grant date	Jan 18, 2022

Abstract

An object of the present invention is to provide a polymerizable liquid crystal compound having excellent solubility, which is used for the formation of an optically anisotropic film having excellent durability, a method for producing the same, a polymerizable liquid crystal composition, an optically anisotropic film, an optical film, a polarizing plate, and an image display device. The polymerizable liquid crystal compound of the embodiment of the present invention is a polymerizable liquid crystal compound represented by Formula (1), L1-SP1-A1-D3-G1-D1-Ar-D2-G2-D4-A2-SP2-L2 . . . (1) in Formula (1), the ClogP value of the group represented by L1-SP1-A1-D3-G1-D1 and the ClogP value of the group represented by L2-SP2-A2-D4-G2-D2 are different from each other, and at least one of the ClogP values is 3.3 or more.

First claim

What is claimed is:

1. A polymerizable liquid crystal compound represented by Formula (1),
L 1 -SP 1 -A 1 -D 3 -G 1 -D 1 -Ar-D 2 -G 2 -D 4 -A 2 -SP 2 -L 2   (1)

in Formula (1), the ClogP value of the group represented by L 1 -SP 1 -A 1 -D 3 -G 1 -D 1 and the ClogP value of the group represented by L 2 -SP 2 -A 2 -D 4 -G 2 -D 2 are different from each other, and
at least one of the ClogP values is 3.3 or more,
wherein in Formula (1), D 1 , D 2 , D 3 , and D 4 each independently represent a single bond, —O—CO—, —C(═S)O—, —CR 1 R 2 —, —CR 1 R 2 —CR 3 R 4 —, —O—CR 1 R 2 —, —CR 1 R 2 —O—CR 3 R 4 —, —CO—O—CR 1 R 2 —, —O—CO—CR 1 R 2 —, —CR 1 R 2 —O—CO—CR 3 R 4 —, —CR 1 R 2 —CO—O—CR 3 R 4 —, —NR 1 —CR 2 R 3 —, or —CO—NR 1 —, and R 1 , R 2 , R 3 , and R 4 each independently represent a hydrogen atom, a fluorine atom, or an alkyl group having 1 to 4 carbon atoms,
G 1 and G 2 each independently represent a divalent alicyclic hydrocarbon group having 5 to 8 carbon atoms, which may have a substituent, and one or more of —CH 2 -'s constituting the alicyclic hydrocarbon group may be substituted with —O—, —S—, or —NH—,
A 1 and A 2 each independently represent an aromatic ring having 6 or more carbon atoms, which may have a substituent, or a cycloalkane ring having 6 or more carbon atoms, which may have a substituent,
SP 1 and SP 2 each independently represent a single bond, a linear or branched alkylene group having 1 to 12 carbon atoms, or a divalent linking group in which one or more of —CH 2 -'s constituting the linear or branched alkylene group having 1 to 12 carbon atoms are substituted with —O—, —S—, —NH—, —N(Q)-, or —CO—, and Q represents a substituent,
L 1 and L 2 each independently represent a monovalent organic group, and at least one of L 1 or L 2 represents a polymerizable group, provided that in a case where Ar is an aromatic ring represented by Formula (Ar-4), at least one of L 1 , L 2 , or L 3 or L 4 in Formula (Ar-4) represents a polymerizable group, and
Ar represents any one aromatic ring selected from the group consisting of groups represented by Formulae (Ar-1) to (Ar-8),

in Formulae (Ar-1) to (Ar-8), *1 represents a bonding position with D 1 and *2 represents a bonding position with D 2 ,
Q 1 represents N or CH,
Q 2 represents —S—, —O—, or —N(R 5 )—, and R 5 represents a hydrogen atom or an alkyl group having 1 to 6 carbon atoms,
Y 1 represents an aromatic hydrocarbon group having 6 to 12 carbon atoms or an aromatic heterocyclic group having 3 to 12 carbon atoms, each of which may have a substituent,
Z 1 represents a monovalent aliphatic hydrocarbon group having 3 to 20 carbon atoms, a monovalent aromatic hydrocarbon group having 6 to 20 carbon atoms, a halogen atom, —OR 6 , —NR 7 R 8 , or —SR 9 , and R 6 to R 9 each independently represent a monovalent aliphatic hydrocarbon group having 3 to 20 carbon atoms or a monovalent aromatic hydrocarbon group having 6 to 20 carbon atoms,
Z 2 represents a hydrogen atom, a monovalent aliphatic hydrocarbon group having 1 to 20 carbon atoms, a monovalent alicyclic hydrocarbon group having 3 to 20 carbon atoms, a monovalent aromatic hydrocarbon group having 6 to 20 carbon atoms, a halogen atom, a cyano group, a nitro group, —OR 10 , —NR 11 R 12 , or —SR 13 , and R 10 to R 13 each independently represent a hydrogen atom or an alkyl group having 1 to 6 carbon atoms,
A 3 and A 4 each independently represent a group selected from the group consisting of —O—, —N(R 14 )—, —S—, and —CO—, and R 14 represents a hydrogen atom or a substituent,
X represents a non-metal atom of Groups 14 to 16 to which a hydrogen atom or a substituent may be bonded,
D 5 and D 6 each independently represent a single bond, —O—CO—, —C(═S)O—, —CR 1 R 2 —, —CR 1 R 2 —CR 3 R 4 —, —O—CR 1 R 2 —, —CR 1 R 2 —O—CR 3 R 4 —, —CO—O—CR 1 R 2 —, —O—CO—CR 1 R 2 —, —CR 1 R 2 —O—CO—CR 3 R 4 —, —CR 1 R 2 —CO—O—CR 3 R 4 —, —NR 1 —CR 2 R 3 —, or —CO—NR 1 —, and R 1 , R 2 , R 3 , and R 4 each independently represent a hydrogen atom, a fluorine atom, or an alkyl group having 1 to 4 carbon atoms,
SP 3 and SP 4 each independently represent a single bond, a linear or branched alkylene group having 1 to 12 carbon atoms, or a divalent linking group in which one or more of —CH 2 -'s constituting the linear or branched alkylene group having 1 to 12 carbon atoms are substituted with —O—, —S—, —NH—, —N(Q)-, or —CO—, and Q represents a substituent,
L 3 and L 4 each independently represent a monovalent organic group, and at least one of L 3 , L 4 , or L 1 or L 2 in Formula (1) represents a polymerizable group,
Ax represents an organic group having 2 to 30 carbon atoms, which has at least one aromatic ring selected from the group consisting of an aromatic hydrocarbon ring and an aromatic heterocyclic ring,
Ay represents a hydrogen atom, an alkyl group having 1 to 12 carbon atoms which may have a substituent, or an organic group having 2 to 30 carbon atoms, which has at least one aromatic ring selected from the group consisting of an aromatic hydrocarbon ring and an aromatic heterocyclic ring,
the aromatic rings in Ax and Ay may have a substituent, and Ax and Ay may be bonded to each other to form a ring, and
Q 3 represents a hydrogen atom or an alkyl group having 1 to 6 carbon atoms which may have a substituent.

2. The polymerizable liquid crystal compound according to claim 1 ,
wherein in Formula (1), the ClogP value of the group represented by L 2 -SP 2 -A 2 -D 4 -G 2 -D 2 is higher than the ClogP value of the group represented by L 1 -SP 1 -A 1 -D 3 -G 1 -D 1 .

3. The polymerizable liquid crystal compound according to claim 1 ,
wherein in Formulae (Ar-1) to (Ar-8), Z 1 represents a monovalent aliphatic hydrocarbon group having 3 to 20 carbon atoms.

4. The polymerizable liquid crystal compound according to claim 2 ,
wherein in Formulae (Ar-1) to (Ar-8), Z 1 represents a monovalent aliphatic hydrocarbon group having 3 to 20 carbon atoms.

5. A method for producing a polymerizable liquid crystal compound, used to synthesize the polymerizable liquid crystal compound according to claim 1 , comprising:
a first esterification step of reacting a compound represented by Formula (2) with a compound represented by Formula (3) to produce a phenol compound; and
a second esterification step of reacting the phenol compound obtained in the first esterification step with a compound represented by Formula (4) to obtain the polymerizable liquid crystal compound according to claim 1 ,
HO—Ar—OH  (2)

L 1 -SP 1 -A 1 -D 3 -G 1 -COOH  (3)

L 2 -SP 2 -A 2 -D 4 -G 2 -COOH  (4),

in Formula (2), Ar represents any one aromatic ring selected from the group consisting of groups represented by Formulae (Ar-1) to (Ar-8),

in Formulae (Ar-1) to (Ar-8), *1 and *2 each represent a bonding position with a hydroxyl group,
Q 1 represents N or CH,
Q 2 represents —S—, —O—, or —N(R 5 )—, and R 5 represents a hydrogen atom or an alkyl group having 1 to 6 carbon atoms,
Y 1 represents an aromatic hydrocarbon group having 6 to 12 carbon atoms or an aromatic heterocyclic group having 3 to 12 carbon atoms, each of which may have a substituent,
Z 1 represents a monovalent aliphatic hydrocarbon group having 3 to 20 carbon atoms, a monovalent aromatic hydrocar

Assignees

• Fujifilm Corp

Inventors

• Hayashi Daisuke
• Shimamura Satoshi
• Takahashi Keita

Classifications

• C09K19/3497 Primary

  the heterocyclic ring containing sulfur and nitrogen atoms · CPC title

• C09K19/24 Primary

  linked by a chain containing nitrogen-to-nitrogen bonds · CPC title

• G02F1/13363

  Birefringent elements, e.g. for optical compensation · CPC title

• G02F1/1335

  Structural association of cells with optical devices, e.g. polarisers or reflectors · CPC title

• C09K2019/0448

  the end chain group being a polymerizable end group, e.g. -Sp-P or acrylate · CPC title