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. 2008 Feb 13;64(Pt 3):m472.
doi: 10.1107/S160053680800319X.

μ(2)-Iodido-bis-{dimeth-yl[methyl-bis(quinolin-8-yl)silanyl-κN,Si,N']platinum(IV)} tetra-kis(penta-fluoro-phen-yl)borate dichloro-methane 0.66-solvate

Affiliations

μ(2)-Iodido-bis-{dimeth-yl[methyl-bis(quinolin-8-yl)silanyl-κN,Si,N']platinum(IV)} tetra-kis(penta-fluoro-phen-yl)borate dichloro-methane 0.66-solvate

C A Marcus Carr et al. Acta Crystallogr Sect E Struct Rep Online. .

Abstract

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 octa-hedral, 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 mol-ecules of dichloro-methane solvent.

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Figures

Fig. 1.
Fig. 1.
ORTEP-3 diagram of compound (I). H atoms are omitted for clarity.
Fig. 2.
Fig. 2.
Packing diagram with co-crystallized dichloromethane shown as the space-filling model.

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