Spectroscopic study on the photophysical properties of chlorine substituted tetraphenylporphyrin-histidine and its zinc(Ⅱ)complexes  

作　　者：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 

出　　处：《Chinese Science Bulletin》2003年第17期1794-1799,共6页

基　　金：supported by the Nationa1 Natural Science Foundation of China(Grant Nos.20072041 and 20133020);the State Kcy Basis Research and Development Plans(Grant No.G1998010100).

摘　　要：The photophysical properties of ortho-Cl, meta-Cl and para-Cl 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 or-tho-chlorine substitution onto the phenyl rings signifi-cantly 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 werequite different from those of meta- and para-substi-tuted compounds. On the other hand, however, theintroduction of covalently-linked histidine did not ex-ert 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 phenylrings.The photophysical properties of ortho-Cl, meta-Cl and para-Cl 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 or-tho-chlorine substitution onto the phenyl rings signifi-cantly 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 werequite different from those of meta- and para-substi-tuted compounds. On the other hand, however, theintroduction of covalently-linked histidine did not ex-ert 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 phenylrings.

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 

分 类 号：O657.3[理学—分析化学]