Document Type
Article
Language
eng
Publication Date
9-2009
Publisher
Springer
Source Publication
Journal of Chemical Crystallography
Source ISSN
0020-1669
Abstract
The thermal reaction of [Os3(CO)10(μ-H)(μ-SN2C4H5)] (1) at 110 °C afforded the new compound [Os3(CO)9(μ-H)(μ 3-η 2-SN2C4H5)] (2) in 84% yield. Compound 2 exists as two isomers, which differ in the disposition of the bridging hydride ligand. Both of the isomers of 2 have been characterized by a combination of elemental analysis, infrared and 1H NMR spectroscopic data together with single crystal X-ray crystallography. The isomers crystallize together in the triclinic space group P-1 with a = 10.4775(2), b = 13.3056(3), c = 15.0325(3) Å, α = 110.8890(10), β = 99.3880(10), γ = 96.1620(10)°, Z = 2 and V = 1900.31(7) Å3.
Recommended Citation
Ghosh, Shishir; Kabir, Shariff E.; Khatun, Mansura; Haworth, Daniel T.; Lindeman, Sergey V.; Siddiquee, Tasneem; and Bennett, Dennis W., "Decarbonylation Reaction of [Os3(CO)10(μ-H)(μ-SN2C4H5)]: X-ray Structures of the Two Isomers of [Os3(CO)9(μ-H)(μ3-η2-SN2C4H5)]" (2009). Chemistry Faculty Research and Publications. 604.
https://epublications.marquette.edu/chem_fac/604
Comments
Accepted version. Journal of Chemical Crystallography, Vol. 39, No. 9 (September 2009): 632-637. DOI. © 2009 Springer. Used with permission.
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