摘要:
Monoperoxo complexes of vanadium(V), M-2[VO(O-2)cmaa (H2O)] (M = K+, NH4+) and M[VO(O-2)Hcmaa (H2O)] (M = K+, Cs+, NBu4+), where cmaa and Hcmaa are anions of (R,S)-N-(carboxymethyl)aspartic acid, H(3)cmaa, were prepared. Based on IR spectra and thermal decomposition characteristics, the heteroligand is proposed to be bound via nitrogen and two carboxylic oxygens, and the water molecule to be coordinated to vanadium. The V-51 NMR spectra of aqueous solutions of dissolved complexes at different pH values are consistent with the presence of the exo - and endo -forms, with chemical shifts at about - 590 and - 600 ppm. Predominantly, the less stable endo -form partially decomposes as the pH is varied. No pH influence on chemical shifts of the diastereomers was observed. (C) 2003 Elsevier B.V. All rights reserved.