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反式-二(吡啶-3-甲酸)四水鈷(Ⅱ)錯合物合成與晶體結構解析

Synthesis and Crystal Structure of Cobalt (Ⅱ) Complex of trans-[Tetraaquabis(pyridine-3-picolinato-κN)-Cobalt(II)]

摘要


A metal complex, trans-[Co(pya)2(H2O)4] (1) (pya = pyridine-3-carboxylic acid), is hydrothermal synthesized from the reaction of CoBr2.xH2O, pyridine-3-carboxylic acid and ethylenediamine. Compound 1 is fully characterized by FT-infrared, elemental analysis and single crystal x-ray diffraction. Crystal data for this complex:Monoclinic, space group: C 1 2 1 (no. 5), a = 14.1623(6) Å, b = 6.8385(3) Å, c = 8.4951(4) Å, β= 118.18(0)∘, V =725.23(6) Å^3, Dx = 1.718 Mg m^(-3), Z=1, R[F^2 > 2σ(F^2)] = 0.0311, wR(F^2) = 0.0896. The title compound, the coordination sphere of the Co(Ⅱ) metal, is octahedral coordination with an approximate D2v symmetry. It is defined by four water molecular O atom and two N atoms from the two pya ligand. In addition, the intermolecular O-H・・・O hydrogen-bonding and π・・・π stacking interactions further extend the title complex to form a 3-D structure.

並列摘要


A metal complex, trans-[Co(pya)2(H2O)4] (1) (pya = pyridine-3-carboxylic acid), is hydrothermal synthesized from the reaction of CoBr2.xH2O, pyridine-3-carboxylic acid and ethylenediamine. Compound 1 is fully characterized by FT-infrared, elemental analysis and single crystal x-ray diffraction. Crystal data for this complex:Monoclinic, space group: C 1 2 1 (no. 5), a = 14.1623(6) Å, b = 6.8385(3) Å, c = 8.4951(4) Å, β= 118.18(0)∘, V =725.23(6) Å^3, Dx = 1.718 Mg m^(-3), Z=1, R[F^2 > 2σ(F^2)] = 0.0311, wR(F^2) = 0.0896. The title compound, the coordination sphere of the Co(Ⅱ) metal, is octahedral coordination with an approximate D2v symmetry. It is defined by four water molecular O atom and two N atoms from the two pya ligand. In addition, the intermolecular O-H・・・O hydrogen-bonding and π・・・π stacking interactions further extend the title complex to form a 3-D structure.

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