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新型噻吩基取代卟啉的合成及其荧光光谱研究
引用本文:陈彰评,端木传嵩,何小平,戴明,杨荣.新型噻吩基取代卟啉的合成及其荧光光谱研究[J].武汉大学学报(理学版),2002,48(4):430-434.
作者姓名:陈彰评  端木传嵩  何小平  戴明  杨荣
作者单位:武汉大学化学与分子科学学院,湖北,武汉,430072
基金项目:国家自然科学基金资助项目 (2 9872 0 3 3 )
摘    要:合成了两种新型噻吩基卟啉-5,15-二(2-噻吩基)-2,8,12,18-四乙基-3,7,13,17-四甲基卟啉7a(45.1%)和5,15-二(2-联噻吩基)-2,8,12,18-四乙基-3,7,13,17-四甲基卟啉7b(61.2%),并研究了它们的光谱性质,其中荧光光谱的最大发射峰蜂都在631nm处,量子产率分别为4.1%(7a)和1.4%(7b)。

关 键 词:噻吩基卟啉  合成  荧光光谱  量子产率
文章编号:0253-9888(2002)04-0430-05
修稿时间:2002年1月20日

Synthesis of New Thiophenylporphyrins and Characterization of Their Fluorescent Spectrum Properties
CHEN Zhang\|ping,DUANMU Chuan\|song,HE Xiao\|ping,DAI Ming,YANG Rong.Synthesis of New Thiophenylporphyrins and Characterization of Their Fluorescent Spectrum Properties[J].JOurnal of Wuhan University:Natural Science Edition,2002,48(4):430-434.
Authors:CHEN Zhang\|ping  DUANMU Chuan\|song  HE Xiao\|ping  DAI Ming  YANG Rong
Abstract:Two new porphyrins 2,8,12,18\|tetraethyl\|3, 7,13,17\|tetramethyl\|5,15\|dithiophenylporphyrin (7a) and 5,15\|dibithiophenyl\|2,8,12,18\|tetraethyl\|3,7,13,17\|tetramethyl\|porphyrin (7b) are synthesized in high yields (45.1% and 61.2% respectively) through the reaction of dipyrrolemehane and thiophenylaldehyde or bithiophenylaldehyde. At the same time the porphyrinogens of these porphyrins can also be getted in high yields (81.3% and 64.7%) from this reaction without adding oxydant. Fluorescent properties of them have been studied. Their maximum fluorescent emissions are both at 631 nm and their quantum yields are 4.1% (7a) and 1.4% (7b) respectively. Spectrums of UV\|Vis fluorescence and H 1 NMR show that with the increment of the substituents in the meso\|positions of porphyrin, the porphyrin's cyclic plane become more nonplanar.
Keywords:synthesis of thiophenylporphyrins  fluorescent spectrum  quantum yield
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