Acta Chimica Sinica ›› 1991, Vol. 49 ›› Issue (2): 199-204. Previous Articles     Next Articles

Original Articles

8-硝基-1-苯基-3, 3-二甲基吲哚苯骈螺吡喃的光化学

吴国生;葛明娟;林光灿;吴碧琪;舒菊坪   

  1. 中国科学院上海有机化学研究所;中国科学院上海光学精密机械研究所
  • 发布日期:1991-02-15

Photochemistry of 8'-nitro-1-phenyl-3, 3-dimethylindolinobenzospiropyran

WU GUOSHENG;GE MINGJUAN;LIN GUANGCAN;WU BIQI;SHU JUPING   

  • Published:1991-02-15

Quantum yields of the photocoloration of the title spiropyran for the direct and benzophenone sensitized photolysis in methanol were 0.38 and 0.53, resp. Biacetyl quenches mainly the triplet photocoloration and to a smaller extent the singlet reaction. From kinetic anal. in the sensitized and quenched reactions, quant. estimation was made of the quantum yields of the primary reactions involved in the direct photolysis. The data suggest that both singlet and triplet of the title spiropyran react to form the colored form. The triplet parameters are as follows: 3t = 2.2 ?10-3 ms; kr = 9.13 ?104 s-1; kd = 8.27 ?104 s-1. Also, the excited triplet state, once populated, is about 2 times more efficient in the formation of the colored form than the excited singlet state.

Key words: INDOLE P, PHOTOCHEMICAL REACTION, BENZENE P, KINETIC ANALYSIS, KETONE, SENSITIZATION, QUANTUM YIELD, QUENCHING, INDOLINOSPIROBENZOPYRAN PHOTOCHROMICS

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