Abstract
Photoinitiated oxidation of dibutyl sulfide (DBS) with air oxygen in a toluene solution of C70 fullerene during irradiation with visible light at a wavelength of 500–700 nm results in the formation of dibutyl sulfone as a main detected product, dibutyl sulfoxide, and butanal. A change in the intensity of radiation incident on the reaction mixture from 2.2 to 44 mW/cm2 insignificantly increases the quantum efficiency of the DBS consumption from 4.5 to 5.9%. The selectivity for sulfoxide increases during the process, while selectivity for sulfone decreases.
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