Issue 5, 2008

Controlling carbon monoxide binding at di-iron units related to the iron-only hydrogenase sub-site

Abstract

Carbon monoxide binding by displacement of a pendant hemi-labile ligand at a di-iron site can be substantially ‘switched-on’ via a ligand protonation pathway which is competitive with metal-metal bond protonation.

Graphical abstract: Controlling carbon monoxide binding at di-iron units related to the iron-only hydrogenase sub-site

Supplementary files

Article information

Article type
Communication
Submitted
20 Aug 2007
Accepted
02 Nov 2007
First published
16 Nov 2007

Chem. Commun., 2008, 606-608

Controlling carbon monoxide binding at di-iron units related to the iron-only hydrogenase sub-site

F. Xu, C. Tard, X. Wang, S. K. Ibrahim, D. L. Hughes, W. Zhong, X. Zeng, Q. Luo, X. Liu and C. J. Pickett, Chem. Commun., 2008, 606 DOI: 10.1039/B712805C

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