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Aggregation of deuteroporphyrin IX diesters in aqueous-organic binary solution
作者姓名:计国桢  胡蕙  张广明  傅伟敏  章道道
作者单位:Shanghai Institute of Organic Chemistry,Chinese Academy of Sciences,Shanghai 200032,China,Department of Chemistry,Fudan University,Shanghai 200433,China,Shanghai Institute of Organic Chemistry,Chinese Academy of Sciences,Shanghai 200032,China,Shanghai Institute of Organic Chemistry,Chinese Academy of Sciences,Shanghai 200032,China,Department of Chemistry,Fudan University,Shanghai 200433,China
摘    要:The aggregation properties of a series of deuteroporphyrin IX diesters in the THF-Buffer (0.1 mol L-1 Tris-HCl) aquiorgano solvent have been studied by means of UV-Vis and fluorescence spectrometers.Experimental data show that the dimerization of porphyrins is mainly determined by π-πinteraction in pure organic solution while further aggregation of porphyrins with long hydrocarbon chains is more likely driven by hydrophobic-lipophilic interaction in aqueous-organic binary solution.The appearance of the aggregates induces a red shift in absorption spectra and fluorescence quenching in fluorescence spectra.The chain-length effect and chain-foldability effect have also been observed.


Aggregation of deuteroporphyrin IX diesters in aqueous-organic binary solution
JI,Guo-Zhen HU,Hui ZHANG,Guang-MinFU,Wei-Min ZHANG,Dao-Dao.Aggregation of deuteroporphyrin IX diesters in aqueous-organic binary solution[J].Chinese Journal of Chemistry,1998,16(5):404-413.
Authors:JI  Guo-Zhen HU  Hui ZHANG  Guang-MinFU  Wei-Min ZHANG  Dao-Dao
Institution:JI,Guo-Zhen HU,Hui ZHANG,Guang-MinFU,Wei-Min ZHANG,Dao-DaoShanghai Institute of Organic Chemistry,Chinese Academy of Sciences,Shanghai 200032,China Department of Chemistry,Fudan University,Shanghai 200433,China
Abstract:The aggregation properties of a series of deuteroporphyrin IX diesters in the THF-Buffer (0.1 mol·L?l Tris-HCl) aquiorgano solvent have been studied by means of UV-Vis and fluorescence spectrometers. Experimental data show that the dimerization of porphyrins is mainly determined by π-π interaction in pure organic solution while further aggregation of porphyrins with long hydro-carbon chains is more likely driven by hydrophobic-lipophilic interaction in aqueous-organic binary solution. The appearance of the aggregates induces a red shift in absorption spectra and fluorescence quenching in fluorescence spectra. The chain-length effect and chain-foldability effect have also been observed.
Keywords:Hydrophobic-lipophilic interactions  deuteroporphyrin IX diesters  aggregation
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