Formation of singlet charge transfer (heteroexcimer) states in the course of the fluorescence quenching of lumiflavin and riboflavin tetrabutyrate by indole and N‐methylindole have been directly observed by means of time‐resolved absorption spectral measurements using a picosecond laser photolysis method. Similar transient spectra have been observed also in the case of a flavoenzyme, D‐amino acid oxidase.
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Karen et al. (1983) studied this question.
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