the nitrite ® nitro isomerization in nitritopentaamine cobalt (iii) halides has been known. in this paper, the effect of the size of the counter ions (noncoordinated groups) on the rate of isomerization in nitritopentaamine cobalt (iii) halides, is reported. the rate of isomerization is decreased by increasing the size of the counter ions. this decrease is explained on the basis of steric inter...

Mediation of reversible deactivation radical polymerization (RDRP) by cobalt(II) complexes (CMRP) is the most highly developed subcategory of organometallic mediated RDRP (OMRP). Attention was paid to CMRP for its unusual high efficiency observed for the control of acrylate and vinyl acetate polymerization that produced homo- and block copolymers with narrow molecular weight distribution and a ...

Preparation and characterization of various complexes of cobalt (III)-amino acid system, especially cobalt (III) glycinato and cobalt (III) alaninato complexes are reported. The identification of the various isomers of these complexes is also reported. The various isomers are separated from their mixture by fractional crystallization. Each of these complexes has been characterized by observing ...

The new [Co(Salen)(PBu3)2]ClO4, [Co(Salen)(PBu3)2]BF4, [Co(Salpn)(PBu3)2]ClO4 and [Co(Salen)(PMe2Ph)2]ClO4 ( where salen = bis(salisylaldehyde)ethylenediimine)) complexes were synthesiszed and chracterized by IR, UV-Vis, 1H NMR spectroscopy and elemental analysis. The IR and 1H NMR spectra cofirmed that the synthesised complexes contain Schiff base ligand, phosphane and conter ion and the eleme...

Some new surfactant-cobalt(III) complex ions of the type, cis-[Co(X)2(C11H23NH2)2] 3+ (where X= ethylenediamine or 2,2’ bipyridyl or 1,10-phenanthroline) and cis-α-Co(trien) (C11H23NH2)2] 3+ were synthesized and characterized by IR, NMR, UV-Visible spectra, elemental and metal analysis. The critical micelle concentration (CMC) values of these surfactant-cobalt(III) complexes in aqueous solution...

a series of complexes of the type trans-[co(acacen)(amine)2]clo4, where (acacen) is the (bis(acetyleacetone) ethylenediimine) and the amines are benzyl amine (bzlan) 1, 2-amino pyrimidine (2ampy) 2, n-methylpipirazine (nmpip) 3, 3-methyl pyridine (3mpy) 4, p-toluidine (p-toldn) 5, has been synthesized and characterized by uv-vis. and ft-ir. the kinetics of the substitution reaction of [co(acace...

Highly reactive tris-carbene Co(I) complexes [(TIMENaryl)Co]Cl react with organic azides to yield monomeric Co(III) imido complexes [(TIMENaryl)Co(NAr')](BPh4) (aryl = mes, xyl; Ar = -C6H4-CH3, -C6H4-OCH3). The cobalt-imido fragment in these complexes is electrophilic and, as a result, the imido group readily inserts into the cobalt-carbene bond, yielding bis-carbene imine cobalt complexes.

Metal-dioxygen adducts are key intermediates detected in the catalytic cycles of dioxygen activation by metalloenzymes and biomimetic compounds. In this study, mononuclear cobalt(III)-peroxo complexes bearing tetraazamacrocyclic ligands, [Co(12-TMC)(O(2))](+) and [Co(13-TMC)(O(2))](+), were synthesized by reacting [Co(12-TMC)(CH(3)CN)](2+) and [Co(13-TMC)(CH(3)CN)](2+), respectively, with H(2)O...

aminocarboxylic acids, such as 2-aminobenzoic acid, react easily with [ir(cod)(pme3)3]cl, (cod=1,5-cyclooctadiene), in thf to produce hydridoaminocarboxylato iridium(iii) complexes in high yields. these octahedral complexes are formed via oxidative addition reaction of the o-h bond of the carboxylic group with the central metal. the starting iridium(i) complex losses the cod molecule, the chlor...