为探讨咪唑环上取代基团对反应平衡的影响,在模拟生理条件(0.15mol·L^-1 NaCl溶液)下,应用多核(^1H、^13C和^51V)、扩散排序谱(DOSY)以及变温NMR等谱学技术研究双过氧钒配合物NH4[OV(O2)2{2-(2'-Pyri—dine)-Imidazole}]·4H2O(简写为bpV(Imi-Py))和咪唑类配体(咪唑、2-甲基-咪唑、4-甲基-咪唑和组氨酸)的相互作用,其从强到弱的顺序为咪唑-4-甲基-咪唑〉2-甲基-咪唑〉组氨酸.研究结果表明,咪唑环上取代基团空间位阻对反应平衡产生较大影响,同时竞争配位的结果导致新的6配位过氧物种[OV(O2)3L]^-(L为咪唑类配体)的生成,当配体为4-甲基-咪唑和组氨酸时,生成的则是一对异构体.
To understand the substituting effects of imidazole ring on the reaction equilibrium, the interactions between diperoxovanadate complex NH4[OV(O2)2{ 2-(2'-Pyridine)-Imidazole}]·4H2O (abbr. bpV(Imi-Py)) and a series of imidazole-like ligands (imidazole, 2-methyl-imidazole, 4-methyl-imidazole, and histidine) in solution were explored using multinuclear (^1H, ^13C, and ^51V) magnetic resonance, diffusion ordered spectroscopy (DOSY), and variable temperature NMR in 0.15 mol .L^-1 NaCl ionic medium for mimicking the physiological conditions. The experimental results indicated that the activities ofbpV(Imi-Py) and organic ligands were as follows: imidazole ≈4-methyl-imidazole〉2-methyl- imidazole〉histidine. The steric effect of the organic ligands affects the reaction equilibrium. At the same time, new six- coordinated peroxovanadate species [OV(O2)2L]- (L= imidazole-like ligands) were formed due to the competitive coordination between 2-(2'-pyridyl)-imidazole and the imidazole-like ligands. When the ligand was 4-methyl- imidazole or histidine, a pair of isomers was formed.