期刊
INORGANIC CHEMISTRY
卷 61, 期 8, 页码 3484-3492出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.1c03386
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资金
- University of Bologna
This article provides a detailed analysis of the electronic structure of the pentanuclear bow tie Au/Fe carbonyl cluster [Au{eta(2)-Fe-2(CO)(8)}(2)](-) and questions the traditional assignment of gold in the +3 oxidation state.
Gold chemistry has experienced in the last decades exponential attention for a wide spectrum of chemical applications, but the +3 oxidation state, traditionally assigned to gold, remains somewhat questionable. Herein, we present a detailed analysis of the electronic structure of the pentanuclear bow tie Au/Fe carbonyl cluster [Au{eta(2)-Fe-2(CO)(8)}(2)](-) together with its two one-electron reversible reductions. A new interpretation of the bonding pattern is provided with the help of inverted ligand field theory. The classical view of a central gold(III) interacting with two [Fe-2(CO)(8)](2-) units is replaced by Au(I), with a d(10) gold configuration, with two interacting [Fe-2(CO)(8)]- fragments. A d(10) configuration for the gold center in the compound [Au{eta(2)-Fe-2(CO)(8)}(2)](-) is confirmed by the LUMO orbital composition, which is mainly localized on the iron carbonyl fragments rather than on a d gold orbital, as expected for a d(8) configuration. Upon one-electron stepwise reduction, the spectroelectrochemical measurements show a progressive red shift in the carbonyl stretching, in agreement with the increased population of the LUMO centered on the iron units. Such a trend is also confirmed by the X-ray structure of the direduced compound [Au{eta(1)-Fe-2(CO)(8)}{eta(2)-Fe-2(CO)(6)(mu-CO)(2)}](3-), featuring the cleavage of one Au-Fe bond.
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