Heteroaromatic isothiocyanates
US-2024124779-A1 · Apr 18, 2024 · US
US9725650B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9725650-B2 |
| Application number | US-201414433674-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 4, 2014 |
| Priority date | Nov 21, 2014 |
| Publication date | Aug 8, 2017 |
| Grant date | Aug 8, 2017 |
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Official abstract text for this publication.
The invention discloses a reactive monomer, a liquid crystal panel and an electronic equipment. The reactive monomer comprises a biphenyl structure and polymeriable groups connecting at both sides of the biphenyl structure, a structure of the reactive monomer is wherein, n≧3 B are the polymerizable groups; the liquid crystal panel in the invention comprises both a first substrate and a second substrate with disposed alignment films respectively, and a liquid crystal layer disposed between the first substrate and the second substrate, and the liquid crystal layer comprises the liquid crystal compound which comprises the reactive monomer. The reactive monomer in the invention can absorb ultra violet light more efficiently, shorten an illuminating time of UV1, and increase production efficiency.
Opening claim text (preview).
The invention claimed is: 1. A reactive monomer, wherein the reactive monomer comprises a biphenyl structure and polymerizable groups connecting at both sides of the biphenyl structure, a formula of the reactive monomer is shown as formula II: Wherein, the X is one of —CF 3 or —CH 3 ; the Y 1 and Y 2 groups are independently —H or —CH 3 ; a wavelength abs…
Physics · mapped topic
Chemistry & Metallurgy · mapped topic
Physics · mapped topic
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Chemistry & Metallurgy · mapped topic
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