影像科学与光化学 ›› 1999, Vol. 17 ›› Issue (3): 264-269.DOI: 10.7517/j.issn.1674-0475.1999.03.264

• 研究简报 • 上一篇    下一篇

两种新型阳离子吲哚啉螺吡喃的合成、表征和光致变色性质的研究

何炜1, 周金渭2, 隋强2, 李仲杰1, 王艳乔2   

  1. 1. 西北大学化学系, 西安710069;
    2. 中国科学院化学研究所, 北京100080
  • 收稿日期:1998-08-24 修回日期:1998-09-15 出版日期:1999-08-20 发布日期:1999-08-20
  • 通讯作者: 隋强

SYNTHESIS, CHARACTERIZATION, ADN INVESTIGATION OF PHOTOCHROMIC PROPERTIES OF TWO NOVEL CATIONIC INDOLINOSPIROPYRANS

HE Wei1, ZHOU Jinwei2, SUI Qiang2, LI Zhongjiea1, WANG Yanqiao2   

  1. 1. Department of Chemistry, Northwest University, Xi’an 710069, P.R. China;
    2. Institute of Chemistry, The Chinese Academy of Sciences, Beijing 100080, P.R. China
  • Received:1998-08-24 Revised:1998-09-15 Online:1999-08-20 Published:1999-08-20

摘要: 螺吡喃是一类重要的光致变色化合物。螺吡喃的正向光致变色是指在紫外光照下,螺吡喃分子的C-O键异裂,由闭环无色体(SP)可逆地变成开环有色体(MC).所形成的有色体可以在暗条件下热致褪色或在可见光照下褪成无色体(示意图1)。

关键词: 吲哚啉螺吡喃, 正向光致变色, 逆向光致变色

Abstract: Two novel cationic indolinospirpoyrans, 1′-(n-butyltriethylammonium iodide)-3′,3′-dimethyl-6-nitro-8-methoxyspiro[2H-1-benzopyran-2,2′-indoline] and 1′-(n-butyltriethylammonium iodide)-3′,3′-dimethyl-6,8-dinitrospiro[2H-1-benzopyran-2,2′-indoline], were synthesized and characterized by suitable methods. The structures and configurations of MC and SP of the two compounds are assigned via their 1H NMR spectra. The photochromism properties of the two compounds were investigated. It was found that the former one shows normal photochromism and the later one shows negative photochromism. The decoloration and coloration process of the two compounds fit first-order kinetics very well, and their rate constants are 1.21×10-2s-1 and 4.0×10-5s-1, respectively.

Key words: indolinospiropyran, normal photochromism, negative photochromism