Article ID Journal Published Year Pages File Type
1236293 Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 2006 7 Pages PDF
Abstract

To understand the substituting effects of organic ligands on the reaction equilibrium, the interactions between diperoxovanadate complex [OV(O2)2(H2O)]− and a series of picoline-like ligands in solution were explored using 1D multinuclear (1H, 13C, and 51V) magnetic resonance, 2D diffusion ordered spectroscopy (DOSY), and variable temperature NMR in 0.15 mol/l NaCl ionic medium for mimicking the physiological conditions. The order of reactive capability of the picoline-like ligands with [OV(O2)2(H2O)]− is found to be picolinamide > N-methylpicolinamide > methyl picolinate > ethyl picolinate ≈ propyl picoliniate > isopropyl picolinate. The substituting group influences the reactivity by either steric effect or electron-donating effect. Competitive coordination interactions result in a series of new seven-coordinated peroxovanadate species [OV(O2)2L]− (L = picoline-like ligands). Their coordination ways were confirmed by density functional calculations.

Related Topics
Physical Sciences and Engineering Chemistry Analytical Chemistry
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