Chemistry of transition-metal clusters with mixed Sb/S ligands: Evidence for a terminal Sb=S double bond in Cp*3Rh3Sb2S5 (Cp* = C5Me5)

Lange, Andreas and Kubicki, Marek M. and Wachter, Joachim and Zabel, Manfred (2005) Chemistry of transition-metal clusters with mixed Sb/S ligands: Evidence for a terminal Sb=S double bond in Cp*3Rh3Sb2S5 (Cp* = C5Me5). INORGANIC CHEMISTRY, 44 (21). pp. 7328-7332. ISSN 0020-1669, 1520-510X

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Abstract

The reaction Of [CP2*Rh2Cl4] (CP* = C5Me5) with a slight excess of K3SbS3 in boiling THF gave the neutral clusters [CP*4Rh4S5] (1), [CP*3Rh3Sb2S5] (2), and after salt metathesis [CP*3Rh3SbSn]PF6 (3; n = 5 and 6). The structures of 1-3 are heterocubane clusters with Cp*Rh, S, and Sb vertices but with sulfur inserted into one (11 and 2) or two (3) edges. X-ray diffraction analysis of 2 additionally reveals a very short Sb-S distance of 2.297(l) A within the novel mu(3)-Sb2S4 ligand. Density functional theory calculation of the model compounds [SSbS](3-), [HSSbS](2-), and [HSSbH2S](0) provided strong evidence for the existence of a stable terminal Sb=S double bond in 2.

Item Type: Article
Uncontrolled Keywords: ORGANOMETALLIC CHALCOGEN COMPLEXES; CRYSTAL-STRUCTURES; SOLID-STATE; ELEMENTS; SULFUR; SULFIDE; ROUTE; NH3; TE;
Subjects: 500 Science > 540 Chemistry & allied sciences
Divisions: Chemistry and Pharmacy > Institut für Anorganische Chemie > Alumni or Retired Professors > Arbeitskreis Dr. Joachim Wachter
Depositing User: Dr. Gernot Deinzer
Date Deposited: 26 Apr 2021 06:13
Last Modified: 26 Apr 2021 06:13
URI: https://pred.uni-regensburg.de/id/eprint/35528

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