Luo Shi-xia, Chen Xiao-jing, Zhu Huai-wu, Zhang Xiao-yi, Wei Gang
School of Chemistry and Materials Science, Guizhou Normal University, Guiyang 550001, China.
Guang Pu Xue Yu Guang Pu Fen Xi. 2012 Mar;32(3):805-8.
The ligand of 2,6-bis[N-(1,1'-dimethyl-2'-hydroxy)carbamoyl]pyridine and its nickel(II) complex were synthesized and characterized by using 1H-NMR, 13C-NMR, FTIR, UV-Vis and elemental analysis, and the complex formulae of C15 H21 N3O4 Ni x H2O were determined. The spectral property of the free ligand and its nickel(II) complex was discussed with the comparison method, and then the structure of nickel(II) complex was determined. The spectral analysis results show that 2,6-bis[N-(1,1'-dimethyl-2'-hydroxy)carbamoyl] pyridine acts as a tridentate ligand, coordinating through two nitrogen atoms of amide anion and one nitrogen atom of aromatic pyridine-ring, and the nickel(II) ion is a four-coordinated geometry with dsp2 hybrid orbitals for bonding these coordinating atoms. The target complex is a square planar low-spin nickel(II) coordination compound, and a nickel(II) ion coordinates to a tridentate ligand and one coordination water molecule.
合成了2,6-双[N-(1,1'-二甲基-2'-羟基)氨基甲酰基]吡啶及其镍(II)配合物,并通过1H-NMR、13C-NMR、FTIR、UV-Vis和元素分析对其进行了表征,确定了配合物的化学式为C15 H21 N3O4 Ni·xH2O。采用比较法讨论了游离配体及其镍(II)配合物的光谱性质,进而确定了镍(II)配合物的结构。光谱分析结果表明,2,6-双[N-(1,1'-二甲基-2'-羟基)氨基甲酰基]吡啶作为三齿配体,通过酰胺阴离子的两个氮原子和芳族吡啶环的一个氮原子进行配位,镍(II)离子为四配位几何结构,采用dsp2杂化轨道与这些配位原子键合。目标配合物是一种平面正方形低自旋镍(II)配位化合物,镍(II)离子与一个三齿配体和一个配位水分子配位。