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单异硫氰基3:1不对称酞菁锌的光谱性质研究
引用本文:陈伟,段武彪,贺春英,左霞,吴谊群.单异硫氰基3:1不对称酞菁锌的光谱性质研究[J].光谱学与光谱分析,2007,27(3):543-546.
作者姓名:陈伟  段武彪  贺春英  左霞  吴谊群
作者单位:[1]黑龙江大学化学化工与材料学院,黑龙江哈尔滨150080 [2]齐齐哈尔大学化学化工学院,黑龙江齐齐哈尔161006
基金项目:黑龙江省教育厅科学技术研究项目(10541170)和黑龙江省自然科学基金项目(132004~05)资助
摘    要:测定了三种含异硫氰基3:1不对称酞菁锌配合物(RO)6(NCS)PcZn(Ⅱ)(R=n-C4 H9;n-C5 H11;n-C10H21)在五种有机溶剂中的电子吸收光谱,研究了取代基和溶剂对吸收光谱的影响和规律。同时测定它们在有机溶剂中的荧光发射光谱,研究了外部取代基、溶剂和浓度对最大发射波长及荧光强度的影响规律,发现此类配合物具有特定的荧光效应,有望成为光动力诊断和治疗的有效光敏剂。

关 键 词:单异硫氰基  不对称酞菁  电子吸收光谱  荧光光谱
文章编号:1000-0593(2007)03-0543-04
收稿时间:2005-12-16
修稿时间:2006-03-26

Spectral study of monoisothiocyanato-substituted 3:1 asymmetrical phthalocyanine zinc(II)]
CHEN Wei , DUAN Wu-biao , HE Chun-ying , ZUO Xia , WU Yi-qun.Spectral study of monoisothiocyanato-substituted 3:1 asymmetrical phthalocyanine zinc(II)][J].Spectroscopy and Spectral Analysis,2007,27(3):543-546.
Authors:CHEN Wei  DUAN Wu-biao  HE Chun-ying  ZUO Xia  WU Yi-qun
Institution:1. College of Chemistry, Chemical Engineering and Material Science, Heilongjiang University, Harbin 150080, China 2. College of Chemistry and Chemical Engineering, Qiqihar University, Qiqihar 161006, China
Abstract:Electronic absorption spectra of three monoisothiocyanato-substituted asymmetrical phthalocyanine zinc(II), 2-isothiocyanato-9,10,16,17,23,24-alkyloxyphthalocyanine zinc(II) (RO)6 (NCS)PcZn(II)] (R = n-C4H9, n-C5H11, n-C10H21), were measured in five organic solvents. The effect and order of the substitute groups and solvents were studied by electronic absorption spectra. The changes of lamda(max) data are very small between monoamino- and monoisothiocyanato-substituted asymmetrical phthalocyanines. The order of lamda(max), data is listed here, CHCl3>CH2Cl2>toluene in non-coordination solvents; DMF>THF in O-coordination solvents. The fluorescence spectra of these complexes were measured in organic solvents at the same time. The effect and order of the substitute groups, solvents and concentrations were studied on the maximum wavelength of emission and fluorescence intensity. The lamda(em,max) data of fluorescence emission are among 690-700 nm. The order of lamda(em,max) data is listed here, DMF>THF in O-coordination solvents and almost the same in non-coordination solvents. The fluorescence intensity is very strong in DMF and THF. The order of fluorescence intensity is listed here, DMF>THF in O-coordination solvents; toluene> CH2Clz > CHCl3 in non-coordination solvents. They have special fluorescent effect and should be expected to become a photosensitizer of photodynamic therapy in future.
Keywords:Monoisothiocyanato group  Asymmetrical phthalocyanine  Electronic absorption spectrum  Fluorescence spectrum
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