Author:
Suzuki Takayoshi,Yamaguchi Hiroshi,Fujiki Masayuki,Hashimoto Akira,Takagi Hideo D.
Abstract
The crystal structures of dichloridopalladium(II), -platinum(II) and -rhodium(III) complexes containing 8-(diphenylphosphanyl)quinoline, (SP-4)-[PdCl2(C21H16NP)], (1) [systematic name: dichlorido(8-diphenylphosphanylquinoline)palladium(II)], (SP-4)-[PtCl2(C21H16NP)]·CH2Cl2, (2) [systematic name: dichlorido(8-diphenylphosphanylquinoline)platinum(II) dichloromethane monosolvate], and (OC-6–32)-[RhCl2(C21H16NP)2]PF6·0.5CH2Cl2·0.5CH3OH, (3) [systematic name:cis-dichloridobis(8-diphenylphosphanylquinoline)rhodium(III) hexafluoridophosphate dichloromethane/methanol hemisolvate] are reported. In these complexes, the phosphanylquinoline acts as a bidentate ligand, forming a planar asymmetrical five-membered chelate ring. The palladium(II) and platinum(II) complex molecules in (1) and (2), respectively, show a typical square-planar coordination geometry and form a dimeric structure through an intermolecular π–π stacking interaction between the quinolyl rings. The centroid–centroid distances between the stacked six-membered rings in (1) and (2) are 3.633 (2) and 3.644 (2) Å, respectively. The cationic rhodium(III) complex in (3) has acis(Cl),cis(P),cis(N)(OC-6–32) configuration of the ligands, in which two kinds of intramolecular π–π stacking interactions are observed: between the quinolyl and phenyl rings and between two phenyl rings, the centroid–centroid distances being 3.458 (2) and 3.717 (2) Å, respectively. The PF6−anion in (3) is rotationally disordered, the site occupancies of each F atom being 0.613 (14) and 0.387 (14). The CH2Cl2and CH3OH solvent molecules are also disordered and equal site occupancies of 0.5 are assumed.
Publisher
International Union of Crystallography (IUCr)
Subject
Condensed Matter Physics,General Materials Science,General Chemistry
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