Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/75028
Title: Why is a proton transformed into a hydride by [NiFe] hydrogenases? An intrinsic reactivity analysis based on conceptual DFT
Authors: Qiu, Siyao
Azofra Mesa, Luis Miguel 
MacFarlane, Douglas R.
Sun, Chenghua
UNESCO Clasification: 2210 Química física
Issue Date: 2016
Journal: Physical Chemistry Chemical Physics 
Abstract: The hydrogen evolution reaction (HER) catalysed by [NiFe] hydrogenases entails a series of chemical events involving great mechanistic interest. In an attempt to understand and delve into the question about ‘Why does nature work in that way?’, an in-depth intrinsic reactivity analysis based on conceptual DFT has been carried out focusing on the so-called I1 to Ni-C step, i.e. our work tries to answer how and why the proton attached to the reactive sulphur atom from one of the exo-cyclic cysteine residues is transformed into a bridging hydride to be shared between the Ni/Fe metals in the active site of [NiFe] hydrogenases, which involves not only H migration, but also a change of the charge state on Ni from Ni(I) to Ni(III). Our DFT results suggest that the transformation is motivated by spontaneous rearrangements of the electron density, and stabilisation comes from the decrease of both electronic activity and electrophilicity index from Ni.
URI: http://hdl.handle.net/10553/75028
ISSN: 1463-9076
DOI: 10.1039/c6cp00948d
Source: Physical chemistry chemical physics [ISSN 1463-9076], 18, n. 22, p. 15369-15374
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