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μ(2)-Iodido-bis­{dimeth­yl[methyl­bis(quinolin-8-yl)silanyl-κ(3) N,Si,N′]platinum(IV)} tetra­kis(penta­fluoro­phen­yl)borate dichloro­methane 0.66-solvate

The title complex, [Pt(2)(CH(3))(4)(C(19)H(15)N(2)Si)(2)I][B(C(6)F(5))(4)]·0.66CH(2)Cl(2), resulted from an attempt to synthesize a stable five-coordinate platinum species via ligand abstraction of a six-coordinate platinum precursor. However, dimerization occurred after ligand abstraction, thereby...

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Detalles Bibliográficos
Autores principales: Carr, C. A. Marcus, Gribble, Christopher W., Gibson, Marcus I.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960829/
https://www.ncbi.nlm.nih.gov/pubmed/21201861
http://dx.doi.org/10.1107/S160053680800319X
Descripción
Sumario:The title complex, [Pt(2)(CH(3))(4)(C(19)H(15)N(2)Si)(2)I][B(C(6)F(5))(4)]·0.66CH(2)Cl(2), resulted from an attempt to synthesize a stable five-coordinate platinum species via ligand abstraction of a six-coordinate platinum precursor. However, dimerization occurred after ligand abstraction, thereby yielding the compound described in this study. The cation is a dinuclear Pt(IV) organometallic complex, in which the metal centers are bridged by an I(−) anion. Both metal centers display a coordination geometry close to octa­hedral, including cis-arranged quinoline ligands connected by Si atoms, which form Pt—Si bonds, two cis-methyl groups, and the bridging I(−) anion. In the crystal structure, voids between cations and anions are partially filled with an average of 0.66 mol­ecules of dichloro­methane solvent.