首页> 外文期刊>Inorganica Chimica Acta >Synthesis, crystal structure and magnetic properties of the one-dimensional chain compound catena-poly[aquabis (4,4 '-bis-1,2,4-triazole-N1)( thiocyanato-N)-manganese-mu-[4,4 '-bis-1,2,4-triazole-N1,N1 ']thiocyanate]
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Synthesis, crystal structure and magnetic properties of the one-dimensional chain compound catena-poly[aquabis (4,4 '-bis-1,2,4-triazole-N1)( thiocyanato-N)-manganese-mu-[4,4 '-bis-1,2,4-triazole-N1,N1 ']thiocyanate]

机译:一维链状化合物链-聚[aquabis(4,4'-双-1,2,4-三唑-N1)(硫氰酸根-N)-锰-mu- [4,]的合成,晶体结构和磁性4'-双-1,2,4-三唑-N1,N1']硫氰酸酯]

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摘要

The structure of [ Mn(btr)(3)(NCS) (H2O)] (NCS) (btr = 4,4'-bis-1,2,4-triazole) was solved by the use of X-ray diffraction methods. The manganese(II) ion is six-coordinated and has both bridging and monodentate btr ligands. Two monodentate btr ligands are cis-oriented and two other btr ligands, also cis-oriented, are bridging between manganese ions, leading to a one-dimensional puckered chain structure running along the [100] direction. One thiocyanate ion and a water molecule complete the hexacoordination and are present in the trans mode. The second thiocyanate ion is not coordinated but is constrained to the complex by a strong hydrogen bond to the water molecule. The torsion angle of the central N-N bond of the btr ligand varies from approximately 90 degrees to as low as 51.6 degrees, caused by steric effects of the lattice NCS anion. Magnetic susceptibility and electron paramagnetic resonance measurements indicate a very weak antiferromagnetic coupling between the manganese(II) ions. Crystal data for [Mn(C4H4N6)(3)(NCS) (H2O)] (NCS): orthorhombic, space group P2(1)2(1)2(1) with a = 6.6946(15), b = 13.559(3), c= 26.607(7) Angstrom, Z=4, V= 2415.2(10) Angstrom(3), R-W = 0.046 on 1915 unique reflections. (C) 1998 Elsevier Science S.A. All rights reserved. [References: 16]
机译:[Mn(btr)(3)(NCS)(H2O)](NCS)(btr = 4,4'-bis-1,2,4-三唑)的结构通过X射线衍射法解决。锰(II)离子是六配位的,具有桥键和单齿btr配体。两个单齿btr配体是顺式的,另外两个btr配体也是顺式的,它们在锰离子之间架桥,导致沿[100]方向延伸的一维褶皱链结构。一个硫氰酸根离子和一个水分子完成六配位并以反式存在。第二硫氰酸根离子不配位,而是通过与水分子的强氢键约束在配合物中。由于晶格NCS阴离子的空间效应,btr配体的中心N-N键的扭转角在大约90度至低至51.6度之间变化。磁化率和电子顺磁共振测量表明,锰(II)离子之间的反铁磁耦合非常弱。 [Mn(C4H4N6)(3)(NCS)(H2O)](NCS)的晶体数据:正交晶系,空间群P2(1)2(1)2(1),a = 6.6946(15),b = 13.559( 3),在1915年唯一反射时,c = 26.607(7)埃,Z = 4,V = 2415.2(10)埃(3),RW = 0.046。 (C)1998 Elsevier Science S.A.保留所有权利。 [参考:16]

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