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Spectroscopic study on the photophysical properties of chlorine substituted tetraphenylporphyrin-histidine and its zinc(Ⅱ)complexes
作者姓名:ZHANGHuijuan  FENGJuan  AIXicheng  ZHANGXingkang  YUZhongheng  ZHANGJianping
作者单位:StateKeyLaboratoryforStructuralChemistryofUnstableandStableSpecies;CenterofMolecularScience,InstituteofChemistry,ChineseAcademvofSciences.Beiiing100080.China
摘    要:The photophysical properties of ortho-CI,meta-CI and para-CI substituted tetraphenylporphy-rin-histidine and their zinc (II) complexes have been studied by means of steady-state absorption and fluo-rescence spectroscopies, as well as time-resolved fluo-rescence spectroscopy. For the cases of both free-base and zinc complexes, it was found that the ortho-chlorine substitution onto the phenyl rings significantly altered the fluorescence quantum yield, thefluorescence lifetime and the ratio between radiative and nonradiative deactivation rates of the porphyrin chromophore, i.e. the photophysical parameters were quite different from those of meta- and para-substituted compounds. On the other hand, however, the introduction of covalently-linked histidine did not exert much effects on the photophysical behavior of the porphyrin chromophore. The results are interpreted interms of the steric effect and the heavy-atom effect from the chlorine atoms substituted onto the phenyl rings.

关 键 词:氯取代四苯基卟啉组氨酸  锌配合物  光谱研究  光物理性质
收稿时间:2003-01-08
修稿时间:2003-04-15

Spectroscopic study on the photophysical properties of chlorine substituted tetraphenylporphyrin-histidine and its zinc (II) complexes
ZHANGHuijuan FENGJuan AIXicheng ZHANGXingkang YUZhongheng ZHANGJianping.Spectroscopic study on the photophysical properties of chlorine substituted tetraphenylporphyrin-histidine and its zinc (II) complexes[J].Chinese Science Bulletin,2003,48(17):1794-1799.
Authors:Huijuan?Zhang  Juan?Feng  Xicheng?Ai  Xingkang?Zhang  Zhongheng?Yu  Email author" target="_blank">Jianping?ZhangEmail author
Institution:ZHANG Huijuan, FENG Juan, AI Xicheng, ZHANG Xingkang, YU Zhongheng & ZHANG Jianping State Key Laboratory for Structural Chemistry of Unstable and StableSpecies; Center of Molecular Science, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100080, China
Abstract:The photophysical properties ofortho- CI,meta-CI andpara-CI substituted tetraphenylporphyrin-histidine and their zinc (II) complexes have been studied by means of steady-state absorption and fluorescence spectroscopies, as well as time-resolved fluorescence spectroscopy. For the cases of both free-base and zinc complexes, it was found that theortho-chlorine substitution onto the phenyl rings significantly altered the fluorescence quantum yield, the fluorescence lifetime and the ratio between radiative and nonradiative deactivation rates of the porphyrin chromophore, i.e. the photophysical parameters were quite different from those ofmeta- andpara-substituted compounds. On the other hand, however, the introduction of covalently-linked histidine did not exert much effects on the photophysical behavior of the porphyrin chromophore. The results are interpreted in terms of the steric effect and the heavy-atom effect from the chlorine atoms substituted onto the phenyl rings.
Keywords:porphyrin-histidine  zinc porphyrin  chlorine substitu-tion  fluorescence spectroscopy  DOI10  1360/03wb0003
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