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Eight-coordinate chelate complexes of zirconium(IV) and niobium(IV): X-ray diffractometric and EPR investigations

机译:锆(IV)和铌(IV)的八配位螯合物:X射线衍射和EPR研究

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The N,N-diethylcarbamato derivative of zirconium(IV), Zr(O2CNEt2)(4) has been studied by X-ray crystallography, Crystal data: C20H40N4O8Zr, monoclinic, space group C2/c, a=14.057(1), b=12.168(1), c=16.746(2) Angstrom, beta=108.071(4)degrees, Z=4, D-c=1.356, F(000) = 1168, T = 213 K. The compound is isotypic with the corresponding niobium(IV) derivative with a dodecahedral coordination at the zirconium atom. By reaction of NbCl4(THF)(2) with Tl(hfacac), the hexafluoroacetylacetonato derivative of niobium(IV), Nb(hfacac)(4), has been prepared and structurally characterized. The compound crystallizes in the orthorhombic space group Pna2(1) with the following cell constants: a = 10.399(4), b = 15.852(9), c = 119.073(1) Angstrom. It is not isotypic with the corresponding zirconium(IV) derivative, Zr(hfacac)(4). Crystal data: C20H4F24O8Zr, monoclinic, space group P2(1), a=11.974(4), b =20.451(6), c=13.140(3) Angstrom, beta=104.487(11)degrees, Z=4, D-c = 1.960, F(000) = 1776, T = 223 K. Although in both compounds the central metal atom shows a square antiprismatic coordination, the coordination mode of the ligands is different and slight deviations from the D-4(llll) and C-2(llss) ideal geometries have been observed in the case of niobium and zirconium, respectively. An EPR study has been performed on the Nb(IV) derivatives as diluted solid solutions in frozen organic solvents or in the diamagnetic matrix of the corresponding zirconium(IV) compound. The EPR spectra have confirmed the presence of non-interacting paramagnets in the solid solutions and, in the case of Nb(O2CNEt2)(4), the point symmetry of the paramagnetic centre has been found to be in agreement with the results of the X-ray investigation. An EPR spectrum of rhombic symmetry has been observed for the hexafluoroacetylacetonato derivative of Nb(IV) when diluted in frozen THF solution or in Zr(hfacac)(4). (C) 1998 Elsevier Science S.A. [References: 51]
机译:锆(IV)的N,N-二乙基氨基甲酸酯衍生物Zr(O2CNEt2)(4)已通过X射线晶体学研究,晶体数据:C20H40N4O8Zr,单斜晶系,空间群C2 / c,a = 14.057(1),b = 12.168(1),c = 16.746(2)埃,beta = 108.071(4)度,Z = 4,Dc = 1.356,F(000)= 1168,T = 213 K.该化合物与相应的铌同型(IV)在锆原子上具有十二面体配位的衍生物。通过NbCl4(THF)(2)与Tl(hfacac)的反应,制备了铌(IV)的六氟乙酰丙酮衍生物Nb(hfacac)(4)并进行了结构表征。该化合物在正交晶空间群Pna2(1)中具有以下晶格常数结晶:a = 10.399(4),b = 15.852(9),c = 119.073(1)埃。它与相应的锆(IV)衍生物Zr(hfacac)(4)不是同型的。晶体数据:C20H4F24O8Zr,单斜晶,空间群P2(1)/ n,a = 11.974(4),b = 20.451(6),c = 13.140(3)埃,beta = 104.487(11)度,Z = 4, Dc = 1.960,F(000)= 1776,T = 223K。尽管在两种化合物中,中心金属原子均显示出方形的反棱镜配位,但配体的配位方式不同,与D-4(III)和在铌和锆的情况下,分别观察到C-2(llss)理想的几何形状。已对Nb(IV)衍生物在冷冻的有机溶剂或相应的锆(IV)化合物的抗磁性基质中的稀释固溶体进行了EPR研究。 EPR光谱已确认固溶体中存在不相互作用的顺磁体,对于Nb(O2CNEt2)(4),顺磁性中心的点对称性与X的结果一致射线调查。在冷冻的THF溶液或Zr(hfacac)(4)中稀释时,已观察到Nb(IV)的六氟乙酰丙酮衍生物的菱形对称EPR光谱。 (C)1998 Elsevier Science S.A. [参考:51]

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