Carbazolyl-containing unsymmetrical photochromicsm di-fragrant alkene monomer or polymer and electrochemical polymerization preparation method thereof
A photochromic and asymmetric technology, applied in chemical instruments and methods, organic chemistry, color-changing fluorescent materials, etc., can solve the problems of low yield, high cost, cumbersome polymerization methods, etc. Stability, significant effect of fatigue resistance
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[0022] Example 1: [Compound 1a]:
[0023] In the general formula, when R is hydrogen, the photochromic compound 1a is constituted, and its name is: poly[1-(2-methylthiophen-3-yl), 2-[2-methyl-5-( N-n-hexylcarbazole) thiophen-3-yl)] perfluorocyclopentene (1a), the structural formula is as follows:
[0024]
[0025] Its synthetic scheme is shown in Scheme 1:
[0026]
[0027] Concrete synthetic steps are as follows:
[0028] 1. 3,5-Dibromo-2-methylthiophene (1)
[0029] Under ice-bath conditions, dissolve 5-methylthiophene (4) (25.617g, 261.4mmol) in acetic acid, add dropwise acetic acid containing liquid bromine under stirring, continue the ice-bath reaction for 8hr., add water solution , the aqueous phase uses Na 2 After neutralization, extract with ether, combine the organic phases, and wash with saturated Na 2 and aqueous solution successively, anhydrous MgSO 4 Drying, filtration, rotary evaporation to remove the solvent, distillation under reduced pressure, ...
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