Restricted rotation of an Fe(CO)2(PL3)-subunit in [FeFe]-hydrogenase active site mimics by intramolecular ligation

Pullen, Sonja and Maji, Somnath and Stein, Matthias and Ott, Sascha (2019) Restricted rotation of an Fe(CO)2(PL3)-subunit in [FeFe]-hydrogenase active site mimics by intramolecular ligation. Dalton Transactions. ISSN 1477-9226

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Abstract

A new series of homodinuclear iron complexes as models of the [FeFe]-hydrogenase active site was prepared and characterized. The complexes of the general formula [Fe2(mcbdt)(CO)5PPh2R] (mcbdt = benzene-1,2-dithiol-3-carboxylic acid) feature covalent tethers that link the mcbdt ligand with the phosphine ligands which are terminally coordinated to one of the Fe centres. The synthetic feasability of the concept is demonstrated with the preparation of three novel complexes. A detailed theoretical investigation showes that by introducing a rigid covalent link between the phosphine and the bridging dithiolate ligands, the rotation of the Fe(CO)2P unit is hindered and higher rotation barriers were calculated compared to non-linked reference complexes. The concept of restricting Fe(L)3 rotation is an approach to kinetically stabilize terminal hydrides which are reactive intermediates in catalytic proton reduction cycles of the enzymes.

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IITH Creators:
IITH CreatorsORCiD
Maji, Somnathhttp://orcid.org/0000-0001-6047-1339
Item Type: Article
Subjects: Chemistry
Divisions: Department of Chemistry
Depositing User: Team Library
Date Deposited: 13 Mar 2019 09:50
Last Modified: 13 Mar 2019 09:50
URI: http://raiithold.iith.ac.in/id/eprint/4877
Publisher URL: http://doi.org/10.1039/C8DT05148H
OA policy: http://www.sherpa.ac.uk/romeo/issn/1477-9226/
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