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|Title:||Chemistry of cyclopentadienyl tricarbonylchromium dimer. Cleavage of bis(thiophosphinyl)disulfanes and bis(thiophosphoryl)disulfanes. Syntheses of CpCr(CO)2(S2PPh2) and CpCr(S2PPh2)2. X-ray crystal structure of CpCr(S2PPh2)2||Authors:||Goh, L.Y.
|Issue Date:||11-Aug-2000||Citation:||Goh, L.Y.,Leong, W.K.,Leung, P.-H.,Weng, Z.,Haiduc, I. (2000-08-11). Chemistry of cyclopentadienyl tricarbonylchromium dimer. Cleavage of bis(thiophosphinyl)disulfanes and bis(thiophosphoryl)disulfanes. Syntheses of CpCr(CO)2(S2PPh2) and CpCr(S2PPh2)2. X-ray crystal structure of CpCr(S2PPh2)2. Journal of Organometallic Chemistry 607 (1-2) : 64-71. ScholarBank@NUS Repository.||Abstract:||The facile reaction of [CpCr(CO)3]2 with one mole equivalent of bis(diphenylthiophosphinyl)disulfane, Ph2P(S)SSP(S)PPh2 led to the isolation of dark purplish brown solids of CpCr(CO)2(S2PPh2) (2) and blue solids of CpCr(S2PPh2)2 (3) in 50 and 10% yields, respectively. Proton NMR spectral studies demonstrated that 3 is derived from 2, the primary product. IR spectral data indicated that 2 possesses cis CO ligands and a bidentate SP(S)Ph2 ligand, whilst 3 contains both a unidentate and a bidentate ligand, as confirmed by its X-ray diffraction analysis. Variable temperature 1H and 31P spectral studies showed the occurrence of very rapid unidentate-bidentate exchange between the ligands in 3 in the temperature range -80-60°C. © 2000 Elsevier Science S.A. All rights reserved.||Source Title:||Journal of Organometallic Chemistry||URI:||http://scholarbank.nus.edu.sg/handle/10635/93292||ISSN:||0022328X|
|Appears in Collections:||Staff Publications|
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