摘要
The property of the lowest excited triplet state of fluorenone (FL) in acetonitrile,ethyl acetate,toluene,cyclohexane has been investigated using time-resolved laser flash photolysis. The appearances of the corresponding cation radicals and anion radicals suggest that the electron transfer reaction occurs between 3FL* and amines. Experimental results show a decrease in the quenching rate constants along with reducing solvent polarity. The change of quenching rate constants of the FL excited triplet with the three N,N-dimethylaniline derivatives are explained using the Hammett constant.
The property of the lowest excited triplet state of fluorenone （FL） in acetonitrile, ethyl acetate, toluene, cyclohexane has been investigated using time-resolved laser flash photolysis. The appearances of the corresponding cation radicals and anion radicals suggest that the electron transfer reaction occurs between 3FL＊ and amines. Experimental results show a decrease in the quenching rate constants along with reducing solvent polarity. The change of quenching rate constants of the FL excited triplet with the three N,N-dimethylaniline derivatives are explained using the Hammett constant.
基金
supported by the National Natural Science Foundation of China (20673108)
