Abstract
In the 2,2′-bipyridine (bipy) catalysed CrVI oxidation of dimethyl sulfoxide (DMSO) to dimethyl sulfone, the CrVI-bipy complex formed at the pre - equilibrium step undergoes a nucleophilic attack by the S or O of DMSO to form a positively charged reactive intermediate. This intermediate experiences an oxygen transfer or a ligand coupling to give the products. The anionic surfactant (SDS) accelerates the process while the cationic surfactant (CPC) retards the reaction.
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Saha, B., Islam, M., & Das, A. K. (2005). Kinetics and mechanism of 2,2′-bipyridine catalysed chromium(VI) oxidation of dimethyl sulfoxide in the presence and absence of surfactants. Journal of Chemical Research, (7), 471–474. https://doi.org/10.3184/030823405774309050
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