Abstract
We provide the first detailed time-resolved mechanistic information on the protonation of a model of the subsite of [FeFe]-hydrogenase, [Fe2(µ-pdt)(CO)4(PMe3)2]; the deceptively simple stoichiometric reaction is shown to be limited by the rate of protonation of the basal–apical isomer followed by its rearrangement to the transoid basal form.
Original language | English |
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Pages (from-to) | 5719-5721 |
Number of pages | 3 |
Journal | Chemical Communications |
Issue number | 38 |
DOIs | |
Publication status | Published - 2009 |