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Title

A topological analysis of the bonding in [M2(CO)10] and [M3(μ-H)3(CO)12] complexes (M = Mn, Tc, Re)

AuthorsMaelen, Juan F. van der ; Cabeza, Javier A.
KeywordsTransition metal carbonyl complexes
Source function (SF)
Electron localization function (ELF)
Quantum theory of atoms in molecules (QTAIM)
Multicenter bonding
Issue Date2016
PublisherSpringer Nature
CitationTheoretical Chemistry Accounts 135: 64 (2016)
AbstractThe M–M, M–H, and M–CO bonding interactions existing in the group 7 transition metal carbonyl complexes [M(CO)] and [M(μ-H)(CO)] (M = Mn, Tc, Re) have been theoretically studied under the perspective of the Quantum Theory of Atoms in Molecules (QTAIM). Several local and integral topological properties of the electron density involved in these interactions, as well as the source function (SF) and the electron localization function, have been computed. The results confirm that the metal atoms in the binuclear [M(CO)] complexes are connected through a localized M–M bond that implicates little electron density (it increases from M = Mn to Tc and Re). On the other hand, such a bonding has not been found in the trinuclear [M(μ-H)(CO)] complexes, which, instead, contain a 6c–6e bonding interaction delocalized over their six-membered M(μ-H) ring, as revealed by the non-negligible non-bonding delocalization indexes. The existence of significant CO to M π-back-donation, slightly higher in the trinuclear clusters than in the binuclear complexes, is indicated by the M···O delocalization indexes and SF calculations.
URIhttp://hdl.handle.net/10261/173161
Identifiersdoi: 10.1007/s00214-016-1821-0
issn: 1432-881X
e-issn: 1432-2234
Appears in Collections:(CINN) Artículos
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