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l-Tyrosinatonickel(II) Complex: Synthesis and Structural, Spectroscopic, Magnetic, and Biological Properties of 2{[Ni(l-Tyr)2(b
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The complex 2{[Ni(l-Tyr)2(bpy)]}路3H2O路CH3OH [1, where l-Tyr = l-tyrosine; bpy = 2,2鈥?bipyridine (2,2鈥?bpy)] was obtained in crystalline form and characterized by X-ray and spectroscopic (FT-IR, NIR鈥搗is鈥揢V, and HFEPR) and magnetic methods. The complex crystallized in the hexagonal system with a = b = 12.8116(18) 脜, c = 30.035(6) 脜, and space group P3221. The six-coordination sphere around the Ni2+ ion is formed by two N and two O l-tyrosinato atoms and completed by two N atoms of the 2,2鈥?bpy molecule. Neighboring [Ni(l-Tyr)2(bpy)] units are joined via weak hydrogen bonds, which create a helical polymeric chain. The coordinated atoms form a strongly distorted cis-NiN2N2鈥睴2 octahedral chromophore. The solid-state electronic spectrum of complex 1 was analyzed assuming D2h symmetry, and the observed bands were assigned to 3B1g 鈫?3Ag, 3B1g 鈫?3B3g, 3B1g 鈫?3B2g, 3B1g 鈫?3B3g, 3B1g 鈫?3B1g, and 3B1g 鈫?3B2g transitions for the I and II d鈥揹 bands, respectively. The crystal-field parameters found for D2h symmetry are Dq = 1066 cm鈥?, Ds = 617 cm鈥?, Dt = 鈭?3 cm鈥?, B22 = 7000 cm鈥?, and Racah B = 812 cm鈥?. Magnetic studies revealed the occurrence of hydrogen-bonded metal pairs. The spin Hamiltonian parameters D = 鈭?.262 cm鈥? and E = 鈭?.1094 cm鈥?, determined from high-field, high-frequency electron paramagnetic resonance spectra, together with a weak antiferromagnetic exchange parameter J = 鈭?.477 cm鈥?, allowed us to reproduce the powder magnetic susceptibility and field-dependent magnetization of the complex. The biological activity of 1 has been tested by using the Fusarium solani, Penicillium verrucosum, and Aspergillus flavus fungi strains and Escherichia coli, Pseudomonas fluorescens, Serratia marcescens, and Bacillus subtilis bacterial strains.

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