Organometallic chalcogen complexes. XX. Stereochemical characterization of an oxidized iron-sulfur dimer, [Fe(h5-C5H5)(CO)(SCH3)]2+. Paramagnetic cation effectively containing a one-electron metal-metal bond

1970 ◽  
Vol 92 (25) ◽  
pp. 7472-7474 ◽  
Author(s):  
Lawrence F. Dahl ◽  
Neil G. Connelly

1986 ◽  
Vol 108 (12) ◽  
pp. 3538-3539 ◽  
Author(s):  
F. Albert. Cotton ◽  
Michael P. Diebold ◽  
Wieslaw J. Roth


ChemInform ◽  
2010 ◽  
Vol 27 (35) ◽  
pp. no-no
Author(s):  
E. CADOT ◽  
V. BEREAU ◽  
B. MARG ◽  
S. HALUT ◽  
F. SECHERESSE
Keyword(s):  


1999 ◽  
Vol 77 (8) ◽  
pp. 1327-1335 ◽  
Author(s):  
Faming Jiang ◽  
Kumar Biradha ◽  
Weng Kee Leong ◽  
Roland K Pomeroy ◽  
Michael J Zaworotko

The following complexes, in which CpIr(CO)2 acts as a 2e donor ligand, have been prepared: Cp(OC)2IrW(CO)5 (1), Cp(OC)2IrRu(CO)3(SiCl3)2, Cp(OC)2IrOs(CO)3(GeCl3)(Cl) (2), Cp(OC)2IrOs(CO)3(X)2 (X = Cl, Br (3), I). The characterization of the complexes included the crystal structures of 1, 2, and 3, which reveal that all contain an unbridged metal-metal bond. The carbonyl ligands of 1 in solution undergo exchange on the NMR time scale above -40°C. With the exception of 2, all the complexes dissociate in solution at room temperature, some rapidly so. Only in the case of 3 is an equilibrium with the dissociation products established. The results indicate that CpIr(CO)2 is a weak ligand.Key words: tungsten, osmium, iridium, binuclear.











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