Indian Association for the Cultivation of Science, 700032, Kolkata, India.
Université Grenoble Alpes, UMR CNRS 5250, Département de Chimie Moléculaire, 38000, Grenoble, France.
Angew Chem Int Ed Engl. 2018 Dec 3;57(49):16001-16004. doi: 10.1002/anie.201808215. Epub 2018 Nov 11.
[NiFe]-hydrogenase enzymes are efficient catalysts for H evolution but their synthetic models have not been reported to be active under aqueous conditions so far. Here we show that a close model of the [NiFe]-hydrogenase active site can work as a very active and stable heterogeneous H evolution catalyst under mildly acidic aqueous conditions. Entry in catalysis is a Ni Fe complex, with electronic structure analogous to the Ni-L state of the enzyme, corroborating the mechanism modification recently proposed for [NiFe]-hydrogenases.
[NiFe]-氢化酶是高效的 H 2 演化催化剂,但迄今为止,其合成模型在水相条件下尚未被报道具有活性。在此,我们表明[NiFe]-氢化酶活性位点的紧密模型可以在温和酸性水相条件下作为一种非常活跃和稳定的非均相 H 2 演化催化剂发挥作用。该催化反应的活性物种是一种具有类似于酶中 Ni-L 态电子结构的 Ni Fe 配合物,这与最近提出的[NiFe]-氢化酶的机理修正相一致。