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光致变色水杨醛缩胺类Schiff碱的荧光性质

Fluorescence of Photochromic Salicylaldehyde-Derived Schiff Bases

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【作者】 赵建章赵冰刘举正王旭仇登利孙丽王宗睦李耀先

【Author】 ZHAO Jian-Zhang~1,2, ZHAO Bing~1, LIU Ju-Zheng~3, WANG Xu~1, QIU Deng-Li~1 SUN Li~1, WANG Zong-Mu~4, LI Yao-Xian~2 (1. The Key Laboratory of Supramolecular Structure and Spectroscopy, Jilin University, Changchun 130023, China; 2. Department of Chemistr

【机构】 吉林大学超分子结构与谱学开放实验室!长春130023吉林大学化学系长春130023吉林大学超分子结构与谱学开放实验室!长春130023东南大学化学化工系!南京210096吉林大学超分子结

【摘要】 测定了双水杨醛缩邻苯二胺 ( 1 )、缩对苯二胺 ( 2 )、缩 1 ,2 -环己二胺 ( 3)、缩乙二胺 ( 4)、缩 1 ,6-己二胺( 5)和水杨醛缩α-苯乙胺 ( 6)在溶液中以及固态时的荧光光谱 ,研究了 Schiff碱 1 ,3,4 ,5和 6在固态和溶液中的光致变色行为 .

【Abstract】 The luminescence and photochromism of a series of six salicylaldehyde-derived Schiff base in solution and solid state were investigated by fluorescence spectroscopy 2,2-[1,2-phenylenebis(nitrilomethylidyne)]bisphenol(1); 2,2-[1,4-phenylenebis(nitrilomethylidyne)]bis-phenol(2); 2,2-[1,2-cyclohexanediylbis(nitrilomethylidyne)]bisphenol(3); 2,2-[1,2-ethane diylbis(nitrilomethylidyne)]bisphenol(4); 2,2-[1,6-hexanediylbis(nitrilomethylidyne)]bisphenol(5); 2-{[(1-phenylethyl)imino]methylidynephenol}(6). The experimental results show that the fluorescence intensity of Schiff base 1~6 is related to the structure of the conjugated system or the carbon bridge linking the two fluorophores in the molecules. The time-resolved fluorescence spectroscopy of 1, 3—6 show that they are photochromic in either solution or solid state(2 is known as a thermochromic one). The time course fluorescence spectroscopy show that the “macro-response” of Schiff bases 3, 5 and 6 with irradiation is extremely rapid, especially for 5, of which the fluorescence intensity changed by about 70% within 10 s.

【基金】 国家自然科学基金!(批准号 :2 96 330 10 )资助
  • 【文献出处】 高等学校化学学报 ,Chemical Research In Chinese Universities , 编辑部邮箱 ,2001年01期
  • 【分类号】O625;O657.3
  • 【被引频次】37
  • 【下载频次】524
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