首页> 外文期刊>International Journal of Quantum Chemistry >Syntheses, crystal structures and magnetic properties of two new bimetallic phosphates M(phen)(H2O)(VO)(H2O)(HPO4)(2) (M = Ni, Co; phen=1,10-phenanthroline)
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Syntheses, crystal structures and magnetic properties of two new bimetallic phosphates M(phen)(H2O)(VO)(H2O)(HPO4)(2) (M = Ni, Co; phen=1,10-phenanthroline)

机译:两种新型双金属磷酸盐M(phen)(H2O)(VO)(H2O)(HPO4)(2)的合成,晶体结构和磁性能(M = Ni,Co; phen = 1,10-phenothroline)

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Two novel layered organic-inorganic hybrid materials M(phen)(H2O)(VO)(H2O)(HPO4)(2) (M = Ni, Co) have been synthesized hydrothermally, their crystal structures and variable temperature magnetic susceptibilities were determined. Being characterized by single-crystal X-ray diffraction, the two compounds are isostructural and crystallize in the monoclinic system with P2(1)/c space group with a = 14.3903(7) Angstrom, b = 15.5232(6) Angstrom, c = 7.3943(3) Angstrom, beta = 90.577(2)degrees, Z = 4, V = 1651.7(2) Angstrom(3) and R-1 = 0.0358 for 1, and a = 14.3726(4) Angstrom, b = 15.5078(5) Angstrom, c = 7.3932(2) Angstrom, beta = 90.576(2)degrees, Z = 4, V = 1647.77(8) Angstrom(3) and R-1 = 0.0323 for 2. The structure exhibits an unusual 4,12-membered rings oxovanadium phosphate (V-P-O) layer capped by [M(phen)](2+) complexes with phen groups projecting above and below into the interlamellar regions. Therefore, the bimetallic phosphate undulating layers extend into three-dimensional supermolecular arrays through a strong pi-pi stacking interaction of the phen groups between adjacent layers. (C) 2004 Elsevier Inc. All rights reserved.
机译:水热合成了两种新型的层状有机-无机杂化材料M(phen)(H2O)(VO)(H2O)(HPO4)(2)(M = Ni,Co),确定了它们的晶体结构和可变磁化率。通过单晶X射线衍射表征,这两种化合物在单斜晶系系统中具有P2(1)/ c空间群,其a = 14.3903(7)埃,b = 15.5232(6)埃,c = 7.3943(3)埃,beta = 90.577(2)度,Z = 4,V = 1651.7(2)埃(3),R-1 = 0.0358(1),a = 14.3726(4)埃,b = 15.5078( 5)埃,c = 7.3932(2)埃,beta = 90.576(2)度,Z = 4,V = 1647.77(8)埃(3),R-1 = 0.0323(对于2)。该结构表现出不寻常的4,由[M(phen)](2+)配合物覆盖的12元环磷酸氧钒钠(VPO)层,其phen组上下突出进入层间区域。因此,双金属磷酸盐起伏层通过相邻层之间的phen基团的强烈的pi-pi堆积相互作用而延伸成三维超分子阵列。 (C)2004 Elsevier Inc.保留所有权利。

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