ELECTRON transfer plays a crucial role in energy transformation of natural biological systemssuch as the photosynthetic process by which plants convert solar energy into chemical energy.This is achieved in photosynthe...ELECTRON transfer plays a crucial role in energy transformation of natural biological systemssuch as the photosynthetic process by which plants convert solar energy into chemical energy.This is achieved in photosynthesis by a series of electron transfers which occur after light is ab-sorbed. Among the various factors which influence the efficiency of electron transfer struc-tural effect is one of the important features to be considered. In recent years, numerous syn-thetic model dyads in which electron donor and electron acceptor are covalently linked by dif-ferent spacers have been designed and synthesized in an effort to understand how the展开更多
Photophysical properties of a porphyrin-phthalocyanine heterodimer covalently linked with a dipentoxy chain have been studied.Absorption spectra show that there is weak exciton coupling between the two chromophores in...Photophysical properties of a porphyrin-phthalocyanine heterodimer covalently linked with a dipentoxy chain have been studied.Absorption spectra show that there is weak exciton coupling between the two chromophores in the ground state.Fluorescence spectra show that intramolecular energy transfer from porphyrin to phthalocyanine moiety occurs in competition with electron transfer.The efficiency of these two processes depends upon the mutual orientation of the two chromophores.The effect of solvent polarity on the intramolecular processes is also discussed.展开更多
Heteroaggregates composed of cationic porphyrin, meso-tetra(p-trimethylamino)-porphyrin iodide, its zinc complex and anionic phthalocyanine sodium hydroxygallium 4,4’,4',4'’-tetrasulfonated phthalocyanine ha...Heteroaggregates composed of cationic porphyrin, meso-tetra(p-trimethylamino)-porphyrin iodide, its zinc complex and anionic phthalocyanine sodium hydroxygallium 4,4’,4',4'’-tetrasulfonated phthalocyanine have been investigated by absorption and fluorescence spectroscopy. It has been found that both free base cationic porphyrin and its zinc complex can form very stable heterodimers with anionic phthalocyanine in water, methanol and dhnethylfonnamide. The stability of the aggregate depends on the polarity as well as the ligation ability of the solvent. No evidence of higher aggregates was detected. Besides axial coordination, steric hindrance which influence the relative orientation of the macrocycles are considered.展开更多
文摘ELECTRON transfer plays a crucial role in energy transformation of natural biological systemssuch as the photosynthetic process by which plants convert solar energy into chemical energy.This is achieved in photosynthesis by a series of electron transfers which occur after light is ab-sorbed. Among the various factors which influence the efficiency of electron transfer struc-tural effect is one of the important features to be considered. In recent years, numerous syn-thetic model dyads in which electron donor and electron acceptor are covalently linked by dif-ferent spacers have been designed and synthesized in an effort to understand how the
基金Project supported by the National Natural Science Foundation of China.
文摘Photophysical properties of a porphyrin-phthalocyanine heterodimer covalently linked with a dipentoxy chain have been studied.Absorption spectra show that there is weak exciton coupling between the two chromophores in the ground state.Fluorescence spectra show that intramolecular energy transfer from porphyrin to phthalocyanine moiety occurs in competition with electron transfer.The efficiency of these two processes depends upon the mutual orientation of the two chromophores.The effect of solvent polarity on the intramolecular processes is also discussed.
基金Project supperted the National Science Foundation of China and the Laboratory of Excited State Processes,Changchun Institute of Physics,Chinese Academy of Science.
文摘Heteroaggregates composed of cationic porphyrin, meso-tetra(p-trimethylamino)-porphyrin iodide, its zinc complex and anionic phthalocyanine sodium hydroxygallium 4,4’,4',4'’-tetrasulfonated phthalocyanine have been investigated by absorption and fluorescence spectroscopy. It has been found that both free base cationic porphyrin and its zinc complex can form very stable heterodimers with anionic phthalocyanine in water, methanol and dhnethylfonnamide. The stability of the aggregate depends on the polarity as well as the ligation ability of the solvent. No evidence of higher aggregates was detected. Besides axial coordination, steric hindrance which influence the relative orientation of the macrocycles are considered.
