Ground-state properties of ruthenium(II) and osmium(II) tin trihydride complexes: A DFT study

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• 作者：Marco Bortoluzzi ; ^a ; ^{markos@unive.it"" rel=""nofollow} ; Gino Paolucci^a ; Bruno Pitteri^a
• 关键词：Ruthenium ; Osmium ; Tin ; DFT ; Hydrides
• 刊名：Polyhedron
• 出版年：2011
• 出版时间：26 May 2011
• 年：2011
• 卷：30
• 期：9
• 页码：1524-1529
• 全文大小：529 K

文摘

DFT methods have been applied for the calculation of several ground-state properties of neutral and charged ruthenium(II) and osmium(II) tin trihydride complexes bearing N-donor, P-donor and C-donor ancillary ligands in their coordination sphere. Complexes of the type M(SnH₃)(Tp)(PPh₃)P(OMe)₃, M(SnH₃)(Cp)(PPh₃)P(OMe)₃ and [M(SnH₃)(Bpy)₂P(OMe)₃]⁺ (M = Ru, Os; Tp = tris(pyrazol-1-yl)borate; Cp = cyclopentadienyl ion; Bpy = 2,2′-bipyridine) have been studied using the EDF2 and B3PW91 functionals. The same calculations have been carried out also on the corresponding [M]–CH₃ and [M]–H compounds, to compare the electronic features of the different reactive ligands coordinated to the same metal fragments. Charge distribution analyses were used to give insight into the roles of the transition metal centres and the ancillary ligands on the properties of the coordinated SnH₃ group. The molecular orbitals of the methyl- and trihydrostannyl-complexes were compared to understand the nature of the [M]–SnH₃ bond and the electronic transitions of these species.