首页> 外文期刊>Inorganica Chimica Acta >Synthesis, characterisation, crystal structures, and magnetic properties of one-dimensional oxalato-bridged metal(II) complexes with 3-hydroxypyridine and isoquinoline
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Synthesis, characterisation, crystal structures, and magnetic properties of one-dimensional oxalato-bridged metal(II) complexes with 3-hydroxypyridine and isoquinoline

机译:含3-羟基吡啶和异喹啉的一维草酸酯桥联金属(II)配合物的合成,表征,晶体结构和磁性

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one-dimensional oxalato-bridged metal(II) compounds of formula [M(mu -ox)(L)(2)](n) [L = 3-hydroxypyridine (pyOH) or isoquinoline (isq)] have been synthesised and characterised by FT-IR spectroscopy, TG-DTA techniques, variable-temperature magnetic measurements and X-ray diffraction methods. The complexes [M(mu -ox)(pyOH)(2)](n) [M = Co (1), Ni (2)] are isomorphous and crystallise in the orthorhombic space group Pnab. The compounds [M(mu -ox)(isq)(2)](n) [M = Co (3), Ni (4), Cu (5)] are also isomorphous and belong to the monoclinic space group C2/c. Crystal structures consist of zig-zag chains in which cis-[M-(L)(2)](2+) units are sequentially bridged by bis-bidentate oxalato ligands with intrachain M . . .M distances in the range 5.38-5.49 Angstrom. The divalent metal centres have a distorted octahedral coordination with four oxygen atoms from two symmetry-related bridging oxalato ligands and the pyridinic nitrogen atoms from two cis-oriented aromatic ligands. Magnetic susceptibility measurements in the temperature range 2.0-300 K show the occurrence of antiferromagnetic intrachain interactions for the compounds 1-4 and a weak ferromagnetic coupling for 5. (C) 2001 Elsevier Science B.V. All rights reserved. [References: 49]
机译:合成并表征了式[M(mu-ox)(L)(2)](n)[L = 3-羟基吡啶(pyOH)或异喹啉(isq)]的一维草酰桥接金属(II)化合物FT-IR光谱,TG-DTA技术,可变温度磁测量和X射线衍射方法。络合物[M(mu -ox)(pyOH)(2)](n)[M = Co(1),Ni(2)]是同构的,并且在正交空间群Pnab中结晶。化合物[M(mu -ox)(isq)(2)](n)[M = Co(3),Ni(4),Cu(5)]也是同构的,属于单斜空间群C2 / c 。晶体结构由之字形链组成,其中顺式[M-(L)(2)](2+)单元由双齿草酸酯配体与链内M顺序连接。 。 .M距离在5.38-5.49埃之间。二价金属中心具有扭曲的八面体配位,其具有来自两个对称相关桥联草酸根配体的四个氧原子和来自两个顺式取向芳族配体的吡啶氮原子。在2.0-300 K温度范围内的磁化率测量表明,化合物1-4发生了反铁磁性链内相互作用,而化合物5则发生了弱铁磁耦合。(C)2001 Elsevier Science B.V.保留所有权利。 [参考:49]

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