Influence of Sequential Thiolate Oxidation on a Nitrile Hydratase Mimic Probed by Multiedge X-ray Absorption Spectroscopy by Jason Shearer, Paige E. Callan, César A. Masitas, and Craig A. Grapperhaus in Inorganic Chemistry (DOI: 10.1021/ic202453c).
They use a range of techniques including multiedge X-ray absorption spectroscopy and some serious hardcore DFT calculations to look at/predict how ionic and how Lewis acidic the complexed metal becomes as the sulphur ligands are sequentially oxygenated. Basically you get a harder Lewis acid as you move from naked sulphur through to a mixed sulfenato/sulfinato species. As the abstract graphic shows....
In the final few paragraphs, they speculate what this means for the mechanism of nitrile hydratase hydration (they say "hydrolysis" but that means the complete breaking up the whole bond to acid and ammonia in my book, not just breaking a couple of pi bonds with a molecule of water.). They show versions of the two most commonly proposed models- metal-bound hydroxide attacking a free floating nitrile, and metal-bound nitrile getting walloped by a hydroxide. They suggest that increasing hardness of the metal centre should favour the attachment of an oxygen based ligand over the nitrogen of a nitrile, and hence favour the metal bound hydroxide model. They end with the comment that harder Lewis acidity would actually aid NHase catalysis whatever was bound to the metal.
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