Synthesis and structure of the rhodium complex [p-Tol4Sb(DMSO-O)]2+[trans-RhBr4(DMSO-S)2][cis-RhBr4(DMSO-S)2]


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The complex [p-(Tol)4Sb(DMSO-O)2+[trans-RhBr4(DMSO-S)2]–[cis-RhBr4(DMSO-S)2] (CIF file CCDC no. 1415243) was synthesized by the reaction of sodium hexabromorhodate with tetra(para-tolyl) stibonium bromide in DMSO and studied by X-ray diffraction. The antimony atoms in two types of crystallographically independent [p-Tol4Sb(DMSO-O)]+ cations have a distorted trigonal-bipyramidal coordination with axially arranged DMSO oxygen atoms (Sb–C, 2.088(9)–2.135(10) Å; Sb∙∙∙O, 2.641(10), 2.690(10) Å). In the octahedral [trans-RhBr4(DMSO-S)2] and [cis-RhBr4(DMSO-S)2] anions, the dimethyl sulfoxide ligands are coordinated to the metal via the sulfur atoms. The Rh–S distances are longer in the trans-isomer (2.333(2), 2.339(2) Å) than in the cis-isomer (2.303(3), 2.318(4) Å).

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V. Sharutin

South Ural State University (National Research University)

编辑信件的主要联系方式.
Email: vvsharutin@rambler.ru
俄罗斯联邦, Chelyabinsk

O. Sharutina

South Ural State University (National Research University)

Email: vvsharutin@rambler.ru
俄罗斯联邦, Chelyabinsk

V. Senchurin

South Ural State University (National Research University)

Email: vvsharutin@rambler.ru
俄罗斯联邦, Chelyabinsk

N. Somov

Lobachevsky State University of Nizhny Novgorod

Email: vvsharutin@rambler.ru
俄罗斯联邦, pr. Gagarina 23, Nizhny Novgorod, 630600

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