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|Title:||Binuclear oxidative addition of Sb-Cl bonds : a facile synthetic route to main group transition element clusters and rings||Authors:||Li, Ying-Zhou
Leong, Weng Kee
|Keywords:||DRNTU::Science::Chemistry::Organic chemistry::Organometallic compounds||Issue Date:||2014||Source:||Li, Y.-Z., Ganguly, R., & Leong, W. K. (2014). Binuclear oxidative addition of Sb-Cl bonds : a facile synthetic route to main group transition element clusters and rings. Organometallics, 33(14), 3867-3876.||Series/Report no.:||Organometallics||Abstract:||Binuclear oxidative addition of Sb–Cl bonds with the clusters Os3(CO)11(NCCH3), 1, or Os3(CO)10(NCCH3)2, 2, was found to be an effective synthetic route to organometallic clusters and rings containing μ2-SbPh2 or μ3-SbPh moieties. Thus, the reaction of SbPh2Cl with 1 afforded the tetranuclear ring Os3(CO)11(Cl)(μ-SbPh2), 3, while its reaction with 2 afforded the pentanuclear ring Os3(CO)10(Cl)2(μ-SbPh2)2, 6. In each case, two or three isomeric products were isolated depending on the reaction conditions. The analogous reaction of SbPhCl2 with 1, on the other hand, afforded the spiked triangular cluster Os3(CO)11(Cl)2(μ3-SbPh), 7, which also existed as two isomers. Pathways for these reactions have been proposed, and the experimental and computational evidence presented.||URI:||https://hdl.handle.net/10356/79501
|DOI:||10.1021/om500565d||Rights:||© 2014 American Chemical Society. This is the author created version of a work that has been peer reviewed and accepted for publication by Organometallics, American Chemical Society. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.1021/om500565d].||Fulltext Permission:||open||Fulltext Availability:||With Fulltext|
|Appears in Collections:||SPMS Journal Articles|
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