Fluoroboron pyrrole liquid crystal compound containing 8-(diphenylethinyl)-ester group flexible multi-element rings, preparation method and application thereof
A bisphenylacetylene and ester-based flexible technology, which is applied in the field of display materials, can solve the problems of lack of performance fluorescent dichroic dyes, achieve the effects of rich types, novel structures, and reduced response time
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Embodiment 1
[0046] Synthesis of liquid crystal dye DC1
[0047](1) Synthesis of ethyl p-iodobenzoate (compound 1)
[0048]
[0049] Add 2.48g of p-iodobenzoic acid and 20ml of ethanol to a 50ml double-necked round-bottom flask for reaction, add a catalytic amount of concentrated sulfuric acid at the same time, heat to reflux, track and monitor by TLC until the reaction is complete, pour into water for extraction with dichloromethane, The excess solvent was removed under reduced pressure to obtain 2.76 g of light yellow oil, with a yield of 85%.
[0050] (2) Synthesis of 4-trimethylsilylethynyl-ethyl benzoate (compound 2)
[0051]
[0052] Add 276mg (8.5mmol) ethyl p-iodobenzoate, 2mL (10mmol) trimethylsilylacetylene, 70mg ditriphenylphosphine palladium dichloride, 150mg triphenylphosphine, and 80mg CuI as catalysts into a 50mL double-port round bottom In the flask, use 15mL of dry triethylamine as an acid-binding agent and solvent. Stir under nitrogen protection and heat to reflu...
Embodiment 2
[0069] Synthesis of liquid crystal dye DC2
[0070] In addition to using propyl bicyclohexyl methyl carbinol instead of pentyl bicyclohexyl carbinol in step (4), replace 4-ethynyl benzene pentyl carbinol with 4-ethynyl phenylpropyl bicyclohexyl methyl carbinol ester in step (6). Except for base bicyclohexylmethanol ester, other operating steps were the same as in Example 1 to obtain 427 mg of red solid with a yield of 62%.
[0071] 1 HNMR (400MHz, CDCl 3 )δ8.05(d, J=8.3Hz, 1H), 7.69(d, J=8.1Hz, 1H), 7.61(d, J=8.3Hz, 1H), 7.32(d, J=8.1Hz, 1H) ,5.99(s,1H),4.14(d,J=6.4Hz,1H),2.56(s,3H),1.88(s,1H),1.78(d,J=8.8Hz,2H),1.71(d, J=13.8Hz, 2H), 1.43(s, 3H), 1.29(dt, J=15.3, 7.7Hz, 2H), 1.18–1.11(m, 2H), 1.04(d, J=15.1Hz, 3H), 1.01–0.91(m,1H),0.87(t,J=7.3Hz,2H).
[0072] 13 CNMR (101MHz, CDCl 3 )δ161.29(s),151.10(s),138.20(s),135.88(s),130.74(s),127.71(s),126.80(s),125.54(s),124.83(s),123.60( s), 122.59(s), 118.87(s), 116.67(s), 86.60(s), 85.28(s), 65.65(s), 55.65(s), 48.69(s), 3...
Embodiment 3
[0075] Synthesis of liquid crystal dye DC3
[0076] In addition to replacing pentyl bicyclohexyl carbinol with cholesterol in step (4), and replacing 4-ethynyl phenylpentyl bicyclohexyl carbinol with 4-ethynyl benzene cholesteryl ester in step (6), other operation steps are the same Example 1, 560 mg of red solid was obtained with a yield of 67%.
[0077] 1 HNMR (400MHz, CDCl 3 )δ8.06(d, J=8.5Hz, 1H), 7.70(d, J=8.3Hz, 1H), 7.62(d, J=8.5Hz, 1H), 7.33(d, J=8.3Hz, 1H) ,6.01(s,1H),5.44(d,J=3.4Hz,1H),4.99–4.83(m,1H),2.58(s,3H),2.49(d,J=7.6Hz,1H),2.13– 1.96(m,2H),1.53(dd,J=13.1,6.6Hz,2H),1.45(s,3H),1.36(d,J=7.9Hz,1H),1.27(s,2H),1.09(s ,2H),1.07–0.96(m,2H),0.94(d,J=6.5Hz,2H),0.89(d,J=1.8Hz,2H),0.88(d,J=1.8Hz,2H),0.71 (s,1H).
[0078] 13 CNMR (101MHz, CDCl 3( s), 128.36(s), 127.26(s), 122.92(s), 121.42(s), 91.31(s), 90.08(s), 74.93(s), 56.72(s), 56.17(s), 50.08( s), 42.35(s), 39.77(s), 39.54(s), 38.24(s), 37.05(s), 36.68(s), 36.22(s), 35.82(s), 31.94(d, J=5.1 Hz), 28.25(s),...
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