Yang Luqin, Crans Debbie C, Miller Susie M, la Cour Agnete, Anderson Oren P, Kaszynski Peter M, Godzala Michael E, Austin LaTanya D, Willsky Gail R
Department of Chemistry, College of Natural Sciences, Colorado State University, Fort Collins, CO 80523-1872, USA.
Inorg Chem. 2002 Sep 23;41(19):4859-71. doi: 10.1021/ic020062l.
The synthesis and characterization of Co(II) and Co(III) 2,6-pyridinedicarboxylate (dipic(2-)) complexes are reported. Solid-state X-ray characterizations were performed on [Co(H(2)dipic)(dipic)].3H(2)O and [Co(dipic)(mu-dipic)Co(H(2)O)(5)].2H(2)O. Two coordination modes not previously observed in dipicolinate transition metal complexes were observed in these complexes; one involves metal coordination to the short C-O (C=O) bond, and the other involves metal coordination to a protonated oxygen atom. Solution studies, including paramagnetic NMR and UV-vis spectroscopy, were done showing the high stability and low lability of the Co(III) complex, whereas the Co(II) complexes exhibited ligand exchange in the presence of excess ligand. The Co(dipic)(2) complex has pH dependent lability and in this regard is most similar to the VO(2)dipic complex. The Co(dipic)(2) was found to be effective in reducing the hyperlipidemia of diabetes using oral administration in drinking water in rats with STZ-induced diabetes. Oral administration of VOSO(4) was used as a positive control for metal efficacy against diabetes. In addition to providing a framework to evaluate structure-function relationships of various transition metal complexes in alleviating the symptoms of diabetes, this work describes novel aspects of structural and solution cobalt chemistry.