REACTIVITY OF ACRIDINE DYE TRIPLET STATES IN ELECTRON TRANSFER REACTIONS

Abstract

Abstract—Rate constants, k q , for the reaction of cationic and neutral acridine orange and 10‐methylacridine orange triplet states ( 3 AOH + , 3 AO, 3 MAO + ) with a series of electron donors have been measured. Two different protolytic forms of the semireduced dye radical are produced by acridine orange triplet quenching at various pH M values in methanolic solution. It is found that k 4 decreases with increasing oxidation potential of the reducing agent for all triplet states in a manner which is expected for electron transfer reactions. The different reactivities of the cationic and neutral triplet forms can, therefore, be attributed to the difference in reduction potentials of these species. The difference in reduction potentials is related to the p K M values of triplet state, p K T M , and semireduced dye radical, p K M S , by thermodynamic consideration. p K T M ( 3 AOH + / 3 AO) is determined to be 11.2. From thisp K S M (AOH./AO;) is estimated to be 17–18. This is in striking contrast to the protolytic equilibrium of the semireduced dye radicals found to be pK F = 4.1. We conclude that the last value represents the second protonation equilibrium (AOH + 2 ./AOH). This conclusion is confirmed by spectroscopic data.