P‐187: Pretilt angle of liquid crystal molecules induced by photo‐aligned films of Polymerized 2‐(methacrylic acid) ethyl 3,5‐diaminobenzoic acid reaction monomer polyimide for PSVA technology
Orientation film is a key material in liquid crystal displays, and the technology of inducing liquid crystal molecular orientation through polyimide photoorientation film is widely studied. In this work, polyimide is a random copolymer synthesized from a mixture of cyclobutanetetracarboxylic dianhyd...
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Published in | SID International Symposium Digest of technical papers Vol. 55; no. 1; pp. 2096 - 2100 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Campbell
Wiley Subscription Services, Inc
01.06.2024
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Subjects | |
Online Access | Get full text |
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Summary: | Orientation film is a key material in liquid crystal displays, and the technology of inducing liquid crystal molecular orientation through polyimide photoorientation film is widely studied. In this work, polyimide is a random copolymer synthesized from a mixture of cyclobutanetetracarboxylic dianhydride and pyromellitic dianhydride, 4,4' ‐ diaminodiphenylmethane, 3,3', 5,5'‐ tetramethylbenzidine, and Methanone, bis (4‐aminophenyl) ‐, homopolymer. In this study, we investigated the pre‐inclination of a series of photo‐crosslinked diamine structures for the polymerization of RM monomers by PSVA (Polymer Stabilized Vertical Alignment) technology, and mainly investigated the pre‐inclination of a series of light‐oriented films with different molar fraction reaction monomers polymerized on the backbone. The results show that the polymerization of 2‐(methacrylate)ethyl ester 3,5‐diaminobenzoic acid reaction monomer with 6.3% molar fraction of polyimide photooriented film achieves high pre‐tilt adjustment under low light accumulation conditions, and successfully achieves excellent optical & reliability performance. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 |
ISSN: | 0097-966X 2168-0159 |
DOI: | 10.1002/sdtp.18017 |