Phase difference plate, circularly polarizing plate, and image display device

Patent metadata

Field	Value
Publication number	US-9995865-B2
Application number	US-201314437399-A
Country	US
Kind code	B2
Filing date	Oct 21, 2013
Priority date	Oct 22, 2012
Publication date	Jun 12, 2018
Grant date	Jun 12, 2018

Abstract

A phase difference plate including an optically anisotropic layer obtained by curing a composition (A) containing a polymerizable liquid crystal compound with reverse wavelength dispersion and a polymerizable monomer, wherein the polymerizable liquid crystal compound with reverse wavelength dispersion has a main chain mesogen and a side chain mesogen bonded to the main chain mesogen in the molecule thereof; the main chain mesogen and the side chain mesogen are oriented in different directions, whereby a birefringence Δn of the optically anisotropic layer has reverse wavelength dispersion property; and retardations of a layer obtained by curing a composition (A0) in which the polymerizable monomer in the composition (A) is replaced by the polymerizable liquid crystal compound with reverse wavelength dispersion and retardations of the optically anisotropic layer satisfy specific relationship; and a circularly polarizing plate and a display device including the same.

First claim

The invention claimed is:

1. A phase difference plate comprising an optically anisotropic layer obtained by curing a composition (A) containing a polymerizable liquid crystal compound with reverse wavelength dispersion and a polymerizable monomer, wherein:
the polymerizable liquid crystal compound with reverse wavelength dispersion has a main chain mesogen and a side chain mesogen bonded to the main chain mesogen in the molecule thereof;
the main chain mesogen and the side chain mesogen of the polymerizable liquid crystal compound with reverse wavelength dispersion are oriented in different directions in the optically anisotropic layer, whereby a birefringence Δn of the optically anisotropic layer has reverse wavelength dispersion property; and
retardations Re0 (450 nm), Re0 (550 nm), and Re0 (650 nm) at wavelengths of 450 nm, 550 nm, and 650 nm of a layer obtained by curing a composition (A0) in which the polymerizable monomer in the composition (A) was replaced by the polymerizable liquid crystal compound with reverse wavelength dispersion and retardations Re (450 nm), Re (550 nm), and Re (650 nm) at wavelengths of 450 nm, 550 nm, and 650 nm of the optically anisotropic layer satisfy relationship of the following expressions (iii) and (iv):
Re0 (450 nm)/Re0 (550 nm)<Re (450 nm)/Re (550 nm)  Expression (iii)

Re0 (650 nm)/Re0 (550 nm)>Re (650 nm)/Re (550 nm)  Expression (iv).

2. The phase difference plate according to claim 1 , wherein
the polymerizable liquid crystal compound with reverse wavelength dispersion is a compound represented by the following formula (I):

[in the formula, Y 1 to Y 6 are each independently a chemical single bond, —O—, —S—, O— C(═O)—, —C(═O)—O—, —O—C(═O)—O—, —NR 1 —C(═O)—, —C(═O)—NR 1 —, —O—C(═O)—NR 1 —, —NR 1 —C(═O)—O—, —NR 1 —C(═O)—NR 1 —, —O—NR 1 —, or —NR 1 —O—, wherein R 1 is a hydrogen atom or an alkyl group having 1 to 6 carbon atoms;
G 1 and G 2 are each independently a divalent aliphatic group having 1 to 20 carbon atoms and optionally having a substituent [the aliphatic group may have one or more of —O—, —S—, —O—C(═O)—, —C(═O)—O—, —O—C(═O)—O—, —NR 2 —C(═O)—, —C(═O)—NR 2 —, —NR 2 —, or —C(═O)— inserted thereinto per one aliphatic group, provided that a case where two or more —O— groups or —S— groups are adjacently inserted is excluded, wherein R 2 is a hydrogen atom or an alkyl group having 1 to 6 carbon atoms];
Z 1 and Z 2 are each independently an alkenyl group having 2 to 10 carbon atoms that may be substituted by a halogen atom;
A x is an organic group of 2 to 30 carbon atoms having at least one aromatic ring selected from the group consisting of an aromatic hydrocarbon ring and an aromatic heterocyclic ring; A y is a hydrogen atom, an alkyl group having 1 to 12 carbon atoms and optionally having a substituent, an alkenyl group having 2 to 12 carbon atoms and optionally having a substituent, a cycloalkyl group having 3 to 12 carbon atoms and optionally having a substituent, —C(═O)—R 3 , —SO 2 —R 6 , or an organic group of 2 to 30 carbon atoms having at least one aromatic ring selected from the group consisting of an aromatic hydrocarbon ring and an aromatic heterocyclic ring, wherein the aromatic ring of A x and A y may have a substituent, and A x and A y may together form a ring, and wherein R 3 is an alkyl group having 1 to 12 carbon atoms and optionally having a substituent, an alkenyl group having 2 to 12 carbon atoms and optionally having a substituent, and a cycloalkyl group having 3 to 12 carbon atoms and optionally having a substituent, and R 6 is an alkyl group having 1 to 12 carbon atoms, an alkenyl group having 2 to 12 carbon atoms, a phenyl group, or a 4-methylphenyl group;
A 1 is a trivalent aromatic group optionally having a substituent;
A 2 and A 3 are each independently a divalent aromatic group having 6 to 30 carbon atoms and optionally having a substituent; and
Q 1 is a hydrogen atom or an alkyl group having 1 to 6 carbon atoms and optionally having a substituent].

3. The phase difference plate according to claim 1 , wherein the polymerizable liquid crystal compound with reverse wavelength dispersion is a compound represented by the following formula (V):

[in the formula Y 1w to Y 8w are each independently a chemical single bond, —O—, —S—, —O—C(═O)—, —C(═O)—O—, —O—C(═O)—O—, —NR 1 —C(═O)—, —C(═O)—NR 1 —, —O—C(═O)—NR 1 —, —NR 1 —C(═O)—O—, —NR 1 —C(═O)—NR 1 —, —O—NR 1 —, or —NR 1 —O—, wherein R 1 is a hydrogen atom or an alkyl group having 1 to 6 carbon atoms;
G 1w and G 2w are each independently a divalent linear aliphatic group having 1 to 20 carbon atoms and optionally having a substituent, wherein the linear aliphatic group may have one or more of —O—, —S—, —O—C(═O)—, —C(═O)—O—, —O—C(═O)—O—, —NR 2w —C(═O)—, —C(═O)—NR 2w —, —NR 2w —, or —C(═O)— inserted thereinto per one aliphatic group, provided that a case where two or more —O— groups or —S— groups are adjacently inserted is excluded, and wherein R 2w is a hydrogen atom or an alkyl group having 1 to 6 carbon atoms;
Z 1w and Z 2w are each independently an alkenyl group having 2 to 10 carbon atoms that may be substituted by a halogen atom;
A xw is an organic group of 2 to 30 carbon atoms having at least one aromatic ring selected from the group consisting of an aromatic hydrocarbon ring and an aromatic heterocyclic ring;
A yw is a hydrogen atom, an alkyl group having 1 to 20 carbon atoms and optionally having a substituent, an alkenyl group having 2 to 20 carbon atoms and optionally having a substituent, an alkynyl group having 2 to 20 carbon atoms and optionally having a substituent, a cycloalkyl group having 3 to 12 carbon atoms and optionally having a substituent, —C(═O)—R 3w , —SO 2 —R 4w , —C(═S)NH—R 9w , or an organic group of 2 to 30 carbon atoms having at least one aromatic ring selected from the group consisting of an aromatic hydrocarbon ring and an aromatic heterocyclic ring, wherein R 3w is an alkyl group having 1 to 20 carbon atoms and optionally having a substituent, an alkenyl group having 2 to 20 carbon atoms and optionally having a substituent, a cycloalkyl group having 3 to 12 carbon atoms and optionally having a substituent, or an aromatic hydrocarbon group having 5 to 12 carbon atoms, R 4w is an alkyl group having 1 to 20 carbon atoms, an alkenyl group having 2 to 20 carbon atoms, a phenyl group, or a 4-methylphenyl group, and R 9w is an alkyl group having 1 to 20 carbon atoms and optionally having a substituent, an alkenyl group having 2 to 20 carbon atoms and optionally having a substituent, a cycloalkyl group having 3 to 12 carbon atoms and optionally having a substituent, or an aromatic group having 5 to 20 carbon atoms and optionally having a substituent, wherein the aromatic ring of A xw and A yw may have a substituent, and A xw and A yw may together form a ring;
A 1w is a trivalent aromatic group optionally having a substituent;
A 2w and A 3w are each independently a divalent alicyclic hydrocarbon group having 3 to 30 carbon atoms and optionally having a substituent;
A 4w and A 5w are each independently a divalent aromatic group having 6 to 30 carbon atoms and optionally having a substituent; and
Q 1w is a hydrogen atom or an alkyl group having 1 to 6 carbon atoms and optionally having a substituent].

4. The phase difference plate according to claim 2 , wherein the polymerizable monomer is a non-liquid crystal compound represented by the following formula (III):

Assignees

• Zeon Corp

Inventors

• Aimatsu Masashi
• Ooishi Hitoshi

Classifications

• G02F1/13363

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

• G02B5/3083 Primary

  Birefringent or phase retarding elements (G02B5/3008, G02B5/3016 take precedence; systems for polarisation control G02B27/286; manufacturing phase modulating patterns by lithographic processes G03F7/001) · CPC title

• C08F28/06

  by a heterocyclic ring containing sulfur · CPC title

• C09K19/3838

  Polyesters; Polyester derivatives · CPC title

• G02B1/04

  made of organic materials, e.g. plastics (G02B1/08 takes precedence) · CPC title