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

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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.

Graphical Abstract

The Ni(II) complex, Ni[C5H4N–C(CH3)=N–N=C(O)–C6H5]2 containing a hydrazone ligand has been generated into which the central Ni(II) atom belongs to a N4O2 coordination environment arised from the enol form of the ligand. It possesses a distorted octahedral geometry.

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Acknowledgments

The authors gratefully acknowledge financial support from the National Science Council of Taiwan. JHH would also like to thank the National Changhua University of Education for the purchase of the CAD-4 diffractometer system.

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Authors and Affiliations

  1. Department of Chemistry, National Changhua University of Education, Changhua, 500, Taiwan

    Amitabha Datta, Nien-Tsu Chuang & Jui-Hsien Huang

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  1. Amitabha Datta
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  2. Nien-Tsu Chuang
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  3. Jui-Hsien Huang
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Correspondence to Jui-Hsien Huang.

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Datta, A., Chuang, NT. & Huang, JH. Synthesis and Structural Characterization of a Nickel(II) Complex with Unsymmetrical NNO-Donor Schiff Base like Hydrazone Ligand. J Chem Crystallogr 41, 1780–1784 (2011). https://doi.org/10.1007/s10870-011-0173-9

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