Anionic fischer-type carbene complexes as bidentate (N,O) ligands
dc.contributor.author | Raubenheimer H.G. | |
dc.contributor.author | Du Toit A. | |
dc.contributor.author | Du Toit M. | |
dc.contributor.author | An J. | |
dc.contributor.author | Van Niekerk L. | |
dc.contributor.author | Cronje S. | |
dc.contributor.author | Esterhuysen C. | |
dc.contributor.author | Crouch A.M. | |
dc.date.accessioned | 2011-05-15T15:59:07Z | |
dc.date.available | 2011-05-15T15:59:07Z | |
dc.date.issued | 2004 | |
dc.description.abstract | New polynuclear complexes, (L1)3 M2{M 2 = Cr(III) (4a, 4b), Fe(III) (5), Co(III) (8)}, (L1) 2M2(L2)2 {M2 = Co(II)(7), Ni(II) (9)}, (L1)2M2(O)L2 {M 2 = V(IV) (6)} and L1M2Cp2 {M 2 = Ti(III) (10)} with L1 = (CO)M1=C{C=NC(CH 3)=CHS}O (M1 = Cr or W) and L2 = 4-methylthiazole or THF, are described. The molecular structures of these complexes determined by X-ray diffraction show that the Fischer-type carbene complexes act as bidentate ligands towards the second metal centre, coordinating through C(carbene)-attached O-atoms and imine N-atoms of the thiazolyl groups to form five-membered chelates with the oxygen atoms in the mer configuration. Isostructural complexes have similar characteristic band patterns in their far-IR spectra. Cyclic voltammetry of selected complexes reveals the oxidation of the carbene complex ligand between 1.01 and 1.29 V. Oxidation of the central metal (M2) takes place at 0.56 and 0.86 V for 7 and 9, respectively. Three stepwise reductions of Cr(III) to Cr(0) occur for 4a and 4b in the region -0.51 to -1.58 V. These new ligand types and other variants thereof should find application in ligand design with the first metal - and other ligands attached thereto - in the carbene complex ligand, playing an important role. | |
dc.description.version | Article | |
dc.identifier.citation | Dalton Transactions | |
dc.identifier.citation | 8 | |
dc.identifier.issn | 14779226 | |
dc.identifier.uri | http://hdl.handle.net/10019.1/11011 | |
dc.subject | Complexation | |
dc.subject | Crystallization | |
dc.subject | Cyclic voltammetry | |
dc.subject | Electrons | |
dc.subject | Gold compounds | |
dc.subject | Molecular structure | |
dc.subject | Molecular vibrations | |
dc.subject | Nuclear magnetic resonance spectroscopy | |
dc.subject | Oxidation | |
dc.subject | Oxygen | |
dc.subject | X ray crystallography | |
dc.subject | X ray diffraction analysis | |
dc.subject | Bidentate ligands | |
dc.subject | Electron pairs | |
dc.subject | Polymetallic complexes | |
dc.subject | Polynuclear complexes | |
dc.subject | Organic compounds | |
dc.title | Anionic fischer-type carbene complexes as bidentate (N,O) ligands | |
dc.type | Article |