Cured film formation composition, orientation material and retardation material
US-10100201-B2 · Oct 16, 2018 · US
US10590219B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10590219-B2 |
| Application number | US-201816104644-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 17, 2018 |
| Priority date | Feb 28, 2014 |
| Publication date | Mar 17, 2020 |
| Grant date | Mar 17, 2020 |
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A retardation material-forming resin composition for providing an orientation material that has high photoreaction efficiency and with which a polymerizable crystal can be aligned in a highly sensitive manner. A retardation material-forming resin composition being thermally curable wherein including a resin (component (A)) having a photo-aligning group to which a thermally reactive moiety is bonded directly or connected via a linking group; an orientation material obtained by use of the composition, and a retardation material formed by use of a cured film obtained from the composition.
Opening claim text (preview).
The invention claimed is: 1. A retardation material-forming resin composition being thermally curable and comprising a resin, component (A), having a photo-aligning group to which a thermally reactive moiety is bonded directly or connected via a linking group, wherein the photo-aligning group is an organic group including a structure of Formula (1): where R is an OH group; and X 1 is a phenylene group that is optionally substituted with an optional substituent. 2. The retardation material-forming resin composition according to claim 1 , wherein the resin of the component (A) is an acrylic copolymer. 3. The retardation material-forming resin composition according to claim 1 , wherein the resin of the component (A) further has a self-crosslinking group, or further has a group that reacts with at least one group A selected from the group consisting of a hydroxy group, a carboxy group, an amide group, an amino group, an alkoxysilyl group, and a group of Formula (2), and when an end portion of the photo-aligning group in the resin is a carboxy group or an amide group, this end portion is also included in the group A, the group of Formula (2) having the structure: where R 5 is an alkyl group, an alkoxy group, or a phenyl group. 4. The retardation material-forming resin composition according to claim 1 , wherein the resin of the component (A) further has at least one group A selected from the group consisting of a hydroxy group, a carboxy group, an amide group, an amino group, an alkoxysilyl group, and a group of Formula (2), and when an end portion of the photo-aligning group in the resin is a carboxy group or an amide group, this end portion is also included in the group A, and the composition further includes a cross-linking agent that reacts with the at least one group A, the group of Formula (2) having the structure: where R 5 is an alkyl group, an alkoxy group, or a phenyl group. 5. The retardation material-forming resin composition according to claim 1 , wherein the resin of the component (A) further has a group that reacts with at least one group A selected from the group consisting of a hydroxy group, a carboxy group, an amide group, an amino group, an alkoxysilyl group, and a group of Formula (2), and when an end portion of the photo-aligning group in the resin is a carboxy group or an amide group, this end portion is also included in the group A, and the group of Formula (2) having the structure: where R 5 is an alkyl group, an alkoxy group, or a phenyl group. 6. The retardation material-forming resin composition according to claim 1 , further comprising a compound having at least two groups A selected from the group consisting of a hydroxy group, a carboxy group, an amide group, an amino group, an alkoxysilyl group, and a group of Formula (2), the group of Formula (2) having the structure: where R 5 is an alkyl group, an alkoxy group, or a phenyl group. 7. The retardation material-forming resin composition according to claim 1 , further comprising a cross-linking catalyst. 8. The retardation material-forming resin composition according to claim 1 , further comprising: a compound having one or more polymerizable groups and at least one group A selected from the group consisting of a hydroxy group, a carboxy group, an amide group, an amino group, an alkoxysilyl group, and a group of Formula (2), or one or more groups that react with the at least one group A, the group of Formula (2) having the structure: where R 5 is an alkyl group, an alkoxy group, or a phenyl group. 9. The retardation material-forming resin composition according to claim 1 , further comprising a monomer having the photo-aligning group to which a thermally reactive moiety is bonded directly or connected via a linking group and one or more polymerizable groups. 10. An orientation material being obtained with the retardation material-forming resin composition as claimed in claim 1 . 11. A retardation material being formed of a cured film that is obtained from the retardation material-forming resin composition as claimed in claim 1 . 12. A thermally cured-film formation composition comprising a resin, component (A), having a photo-aligning group to which, a thermally reactive moiety is bonded directly or connected via a linking group, wherein the photo-aligning group is an organic group including a structure of Formula (1): where R is an OH group; and X 1 is a phenylene group that is optionally substituted with an optional substituent. 13. The thermally cured-film formation composition according to claim 12 , wherein the resin of the component (A) is an acrylic copolymer. 14. The thermally cured-film formation composition according to claim 12 , wherein the resin of the component (A) further has a self-crosslinking group, or further has a group that reacts with at least one group A selected from the group consisting of a hydroxy group, a carboxy group, an amide group, an amino group, an alkoxysilyl group, and a group of Formula (2) and when an end portion of the photo-aligning group in the resin is a carboxy group or an amide group, this end portion is also included in the group A, the group of Formula (2) having the structure: where in the Formula, R 5 is an alkyl group, an alkoxy group, or a phenyl group. 15. The thermally cured-film formation composition according to claim 12 , wherein the resin of the component (A) further has at least one of group A selected from the group consisting of a hydroxy group, a carboxy group, an amide group, an amino group, an alkoxysilyl group, and a group of Formula (2), and when an end portion of the photo-aligning group in the resin is a carboxy group or an amide group, this end portion is also included in the group A, and the composition further includes a cross-linking agent that reacts with the at least, one group A, the group of Formula (2) having the structure: where R 5 is an alkyl group, an alkoxy group, or a phenyl group. 16. The thermally cured-film formation composition according to claim 12 , wherein the resin of the component (A) further has a group that reacts with at least one group A selected from the group consisting of a hydroxy group, a carboxy group, an amide group, an amino group, an alkoxysilyl group, and a group of Formula (2), and when an end portion of the photo-aligning group in the resin is a carboxy group or an amide group, this end portion is also included in the group A, the group of Formula (2) having the structure: where R 5 is an alkyl group, an alkoxy group, or
by light irradiation, e.g. linearly polarised light photo-polymerisation · CPC title
made of organic materials, e.g. plastics (G02B1/08 takes precedence) · CPC title
of polyhydric alcohols or phenols {, e.g. 2-hydroxyethyl (meth)acrylate or glycerol mono-(meth)acrylate} · CPC title
Homopolymers or copolymers of acids; Metal or ammonium salts thereof · CPC title
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
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