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Femtosecond UV photochemistry of the biologically relevant L-cysteine disulfide moiety in aqueous solution investigated by time-resolved X-ray absorption spectroscopy

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Abstract

Femtosecond X-ray absorption spectroscopy of the disulfide bridge in L-cystine reveals the thyil radical as the only primary photoproduct which geminately recombines in an ultrafast solvent cage-mediated process, leading to the long-lived perthyil radical.

© 2022 The Author(s)

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