Reactions of Cp*3Co3(μ2-H)3(μ3-H) with Carbon Dioxide, Carbon Disulfide, and Phenyl Isocyanate

Published

Journal Article

The tetrahydride tricobalt cluster Cp*3Co3(μ2-H)3(μ3-H) (1) reduces CO2 at 120 °C to form the dicobalt dicarbonyl complex [Cp*Co(μ-CO)]2 (2) in 45% yield by 1H NMR. 1 reacted with CS2 at room temperature to form the thiocarbonyl cluster Cp*3Co3(μ3-CS)(μ3-S) (3) in 19% isolated yield. 3 was characterized by X-ray crystallography and shown to consist of a triangle of cobalt atoms [Co-Co(aVe) = 2.495 Å] capped on one face by a μ3-sulfide ligand [Co-μ3-S(ave) = 2.129 Å] and on the opposite face by a μ3-thiocarbonyl ligand [Co- μ3-C(ave) = 1.949, μ3-C-S = 1.634(5) Å]. 1 reacted with phenyl isocyanate at 55 °C to form the N,N′-diphenylureylene complex Cp*2Co2(μ2,μ2-η2-PhNCONPh) (5), the dicarbonyl tricobalt cluster Cp*3Co3(μ3-CO)2 (6), and the carbonyl dimer 2. 5 was isolated in 13% yield and characterized by X-ray crystallography, which revealed that each nitrogen atom of the η2-N,N′-diphenylureylene ligand was symmetrically bonded to both cobalt atoms [Co-Co = 2.456-(1), Co-μ2-N(ave) = 1.959 Å]. © 1995, American Chemical Society. All rights reserved.

Full Text

Duke Authors

Cited Authors

  • Casey, CP; Widenhoefer, RA; Hayashi, RK

Published Date

  • March 1, 1995

Published In

Volume / Issue

  • 34 / 5

Start / End Page

  • 1138 - 1144

Electronic International Standard Serial Number (EISSN)

  • 1520-510X

International Standard Serial Number (ISSN)

  • 0020-1669

Digital Object Identifier (DOI)

  • 10.1021/ic00109a022

Citation Source

  • Scopus