Issue 1, 2017

Carbon dioxide binding at a Ni/Fe center: synthesis and characterization of Ni(η1-CO2C) and Ni-μ-CO2C2O,O′-Fe

Abstract

The degree of CO2 activation can be tuned by incorporating a distinct electronic coordination environment at the nickel center. A mononuclear nickel carboxylate species (Ni–CO2, 3) and a dinuclear nickel–iron carboxylate species (Ni–CO2–Fe, 5) were prepared. The structure of 3 reveals a rare η1C binding mode of CO2, while that of 5 shows bridging CO2 binding (μ2C2O,O′) between the nickel and iron, presented as the first example of a nickel-μ-CO2-iron species. The structural analyses of 3 and 5 based on XRD and DFT data reveal a higher degree of CO2 activation in 5, imparted by the additional interaction with an iron ion.

Graphical abstract: Carbon dioxide binding at a Ni/Fe center: synthesis and characterization of Ni(η1-CO2-κC) and Ni-μ-CO2-κC:κ2O,O′-Fe

Supplementary files

Article information

Article type
Edge Article
Submitted
03 Aug 2016
Accepted
30 Aug 2016
First published
30 Aug 2016
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2017,8, 600-605

Carbon dioxide binding at a Ni/Fe center: synthesis and characterization of Ni(η1-CO2C) and Ni-μ-CO2C2O,O′-Fe

C. Yoo and Y. Lee, Chem. Sci., 2017, 8, 600 DOI: 10.1039/C6SC03450K

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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