化学学报 ›› 2008, Vol. 66 ›› Issue (22): 2476-2482. 上一篇    下一篇

研究论文

取代吡啶与双过氧钒配合物相互作用的NMR和理论研究

于贤勇a,b 张 峻b 易平贵*,a,b 彭洪亮a
郑柏树a 黄昊文a,b 陈 忠b

  

  1. (a湖南科技大学化学化工学院 分子构效关系湖南省普通高等学校重点实验室 湘潭 411201)
    (b厦门大学物理系 固体表面物理化学国家重点实验室 厦门 361005)

  • 投稿日期:2008-04-17 修回日期:2008-06-25 发布日期:2008-11-28
  • 通讯作者: 易平贵

NMR and Theoretical Study on Interactions between Diperoxovanadate Complex and Substituted Pyridines

YU, Xian-Yonga,b ZHANG, Junb YI, Ping-Gui*,a,b PENG, Hong-Lianga
ZHENG, Bai-Shua HUANG, Hao-Wena,b CHEN, Zhongb
  

  1. (aHunan Province College Key Laboratory of QSAR/QSPR, School of Chemistry and Chemical Engineering, Hunan University of Science and Technology, Xiangtan 411201)
    (bState Key Laboratory for Physical Chemistry of Solid Surface, Department of Physics, Xiamen University, Xiamen 361005)
  • Received:2008-04-17 Revised:2008-06-25 Published:2008-11-28
  • Contact: YI, Ping-Gui

为探讨有机配体上取代基团对反应平衡的影响, 在模拟生理条件下(0.15 mol/L NaCl溶液), 应用多核(1H, 13C和51V)多维(DOSY)以及变温NMR技术研究双过氧钒配合物[OV(O2)2(D2O)]-/[OV(O2)2(HOD)]-(简写为bpV)与取代吡啶的相互作用. bpV与有机配体的反应性从强到弱的顺序为: 皮考林酸根>异烟酸根>异烟酸甲酯>皮考林甲酯, 这说明吡啶环上同一位置上的不同取代基团和同一取代基团在不同位置上都影响反应平衡, 竞争配位导致一系列新的6配位(配体为异烟酸根和异烟酸甲酯)或7配位(配体为皮考林酸根和皮考林甲酯)的过氧钒物种[OV(O2)2L]n- (L=取代吡啶, n=1或2)生成, 密度泛函计算结果较合理地解释了实验结果, 并表明溶剂化在反应中起重要作用.

关键词: cmd=search&, term=">双过氧钒配合物, 取代吡啶, 相互作用, 核磁共振, 理论计算

To understand the substitution group effects of organic ligands on the reaction equilibrium, the interactions between diperoxovanadate complex [OV(O2)2(D2O)]-/[OV(O2)2(HOD)]- (abbr. bpV) and a series of substituted pyridines were explored using multinuclear (1H, 13C, and 51V) magnetic resonance, DOSY, and variable temperature NMR in 0.15 mol/L NaCl ionic medium for mimicking the physiological condition. The reactivity order among the substituted pyridines and bpV is picolinate>isonicotinate>methyl isonicotinate>methyl picolinate. The competitive coordination results in the formation of a series of new six-coordinated (isonicotinate and methyl isonicotinate) or seven-coordinated (picolinate and methyl picolinate) peroxovanadate species [OV(O2)2L]n- (L=substituted pyridines, n=1 or 2). Both the different substitution groups at the same position and the same groups at the different substitution position affect these reactions. The results of density functional calculations provide someway a reasonable explanation for the relative reactivity of the substituted pyridines. Solvation effects play an important role in these reactions.

Key words: diperoxovanadate, substituted pyridine, interaction, NMR, theoretical calculation