Self-alignment additive for liquid crystal medium, and preparation method and application of self-alignment additive
A liquid crystal medium, self-alignment technology, applied in liquid crystal materials, chemical instruments and methods, optics, etc., can solve the problems of cumbersome coating process of PI alignment film, weak anchoring ability of liquid crystal molecules, affecting the performance of liquid crystal medium, etc., and achieve low temperature work Excellent effect, excellent performance, high optical anisotropy effect
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Embodiment 1
[0086] The structural formula of the liquid crystal compound is:
[0087]
[0088] The synthetic route for preparing compound BYLC-01 is as follows:
[0089]
[0090] Specific steps are as follows:
[0091] (1) Synthesis of compound BYLC-01-1:
[0092] Under nitrogen protection, add 35g (0.287mol), 150ml tetrahydrofuran, add dropwise 0.37mol n-butyllithium n-hexane solution at -70~-80°C under temperature control, react with temperature control for 1 hour after dropping, then add 46.6g boric acid dropwise under temperature control at -60~-70°C Trimethyl ester (0.44mol), and then naturally warmed to -30°C. Add 400ml of 2M hydrochloric acid aqueous solution for acidification, perform conventional post-treatment, and recrystallize from petroleum ether to obtain 43.0g of light yellow solid (compound BYLC-01-1, 0.259mol), HPLC: 99.7%, yield: 90.2%.
[0093] (2) Synthesis of compound BYLC-01-2:
[0094] Under the protection of nitrogen, add 43.0g compound BYLC-01-1 (0.259...
Embodiment 3
[0104] The structural formula of the liquid crystal compound is:
[0105]
[0106] The synthetic route for preparing compound BYLC-02 is as follows:
[0107]
[0108] Specific steps are as follows:
[0109] (1) Synthesis of compound BYLC-02-1:
[0110] Add 35g to the reaction bottle (0.287mol), 450ml tetrahydrofuran, add dropwise 0.315mol n-butyllithium n-hexane solution at -70~-80℃ under temperature control, react for 1 hour under temperature control after dropping, add 59.7g dropwise under temperature control at -70~-80℃ and 100ml of tetrahydrofuran, then naturally warmed to -30°C, added 500ml of 2M hydrochloric acid aqueous solution for acidification, performed conventional post-treatment, and spin-dried the solvent to obtain 88.8g (0.269mol) of light yellow liquid (compound BYLC-02-1) . GC: 91.3% (cis+trans), yield: 93.7%.
[0111] (2) Synthesis of compound BYLC-02-2:
[0112] Add 88.8g of compound BYLC-02-1 (0.269mol), 0.84g of p-toluenesulfonic acid, 500ml of...
Embodiment 4
[0118] According to the technical scheme of Example 3, the following compounds can be synthesized by simply replacing the corresponding raw materials without changing any substantive operations:
[0119]
[0120] R represents an alkyl or alkoxy group having 1-5 carbon atoms; n represents 0, 1, 2, 3, 4 or 5.
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