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Synthesis and Structural Characterization of a Nickel(II) Complex with Unsymmetrical NNO-Donor Schiff Base like Hydrazone Ligand

机译:具有不对称NNO-施诺夫席夫碱的Hy(II)配合物的合成和结构表征

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Abstract The nickel(II) complex Ni[C5H4N–C(CH3)=N–N=C(O)–C6H5]2 (1), containing the potentially tridentate Schiff base like hydrazone ligand (LH) which is the 1:1 condensation product of benzhydrazide and 2-acetylpyridine, was prepared and characterized by IR and UV–Vis spectra, thermal analysis and single crystal X-ray diffraction measurements. Structural investigation shows that the molecule prefers a monoclinic lattice, having space group Cc, a = 10.248(6), b = 19.692(11), c = 12.281(7) Å, β = 91.523(10)º, Z = 4. The central Ni atom is in N4O2 coordination sphere developed with the NNO donor sets of the two independently Schiff base like hydrazone ligands with the two Ni–N(pyridine) bonds being significantly longer than the two Ni–N(imino) bonds, 2.096(6), 2.105(6) versus 1.972(6), 2.008(6) Å. The two Ni(II) amide-O bond distances of the chelating ligands are 2.090(6) and 2.092(6) Å respectively.
机译:摘要镍(II)配合物Ni [C 5 H 4 N–C(CH 3 )= N–N = C(O) –C 6 H 5 ] 2 (1),其中包含潜在的三齿席夫碱,如配体(LH),为1:1制备了苯肼与2-乙酰基吡啶的缩合产物,并通过红外和紫外-可见光谱,热分析和单晶X射线衍射测量进行了表征。结构研究表明,该分子更喜欢单斜晶格,其空间群为Cc,a = 10.248(6),b = 19.692(11),c = 12.281(7)Å,β= 91.523(10)º,Z = 4。中心的Ni原子在N 4 O 2 配位球中,由两个独立的席夫碱(如配体)的NNO供体集和两个Ni–N(吡啶)形成键显着长于两个Ni–N(亚氨基)键2.096(6),2.105(6)对1.972(6),2.008(6)Å。螯合配体的两个Ni(II)酰胺-O键距离分别为2.090(6)和2.092(6)。

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