Abstract
A series of cobalt complexes, stabilized by a monoanionic tridentate NCN pincer ligand, was synthetized and characterized. Preparation of the paramagnetic 15 VE complex [Co(NCN(CH2)-Et)Br] (1) was accomplished by transmetalation of Li[2,6-(Et(2)NCH(2))(2)C(6)H(3)] with CoBr(2) in THF. Treatment of this air-sensitive compound with NO gas resulted in the formation of the diamagnetic Co(III) species [Co(NCN(CH2)-Et)(NO)Br] (2) as confirmed by X-ray diffraction. This complex features a strongly bent NO ligand (Co-N-O∠135.0°). The ν(NO) is observed at 1609 cm(-1) which is typical for a bent metal-N-O arrangement. Coordinatively unsaturated 1 could further be treated with pyridine, isocyanides, phosphines and CO to form five-coordinate 17 VE complexes. Oxidation of 1 with CuBr(2) led to the formation of the Co(III) complex [Co(NCN(CH2)-Et)Br(2)]. Treatment of [Co(NCN(CH2)-Et)Br(2)] with TlBF(4) as halide scavenger in acetonitrile led to the formation of the cationic octahedral complex [Co(NCN(CH2)-Et)(MeCN)(3)](BF(4))(2). A combination of X-ray crystallography, IR-, NMR- and EPR-spectroscopy as well as DFT/CAS-SCF calculations were used to characterize all compounds.