首页> 外文期刊>Journal of the Chemical Society, Dalton Transactions. Inorganic Chemistry >X-Ray diffraction and magnetic studies on a series of isostructural divalent metal chloranilates with zigzag polymeric chain structures and on a dinuclear iron(III) chloranilate
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X-Ray diffraction and magnetic studies on a series of isostructural divalent metal chloranilates with zigzag polymeric chain structures and on a dinuclear iron(III) chloranilate

机译:一系列具有锯齿形聚合物链结构的同构二价金属氯胺酸盐和双核氯胺铁的X射线衍射和磁性研究

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The reaction of iron(III) ion with chloranilic acid (2,5-dichloro-3,6-dihydroxycyclohexa-2,5-diene-1,4-dione) in hot aqueous solution in air generated a product in which the iron, surprisingly, is in the +II oxidation state as is indicated by structural, magnetic and Mossbauer spectral studies. Single crystal X-ray studies of the product of composition [Fe(C6Cl2O4)(H2O)(2)]. H2O reveal a 1-dimensional zigzag polymeric structure with iron(II) ions carrying two cis water ligands linked together by bridging chloranilate anions. Hydrogen bonding between lattice water and the chains, together with close stacking of C6Cl2 units from adjacent chains, leads to a very compact 3-dimensional network. The same product can be generated directly from iron(II) ion. Weak ferromagnetic coupling between high spin iron(II) centres with J=+0.47 cm(-1) is observed. Isostructural crystalline materials can be obtained in which Fe-II has been replaced by Mn-II, Zn-II and Cd-II, a complete structural refinement being carried out in the latter case. Very weak antiferromagnetic coupling between high spin metal centres is observed in the manganese case (J=-0.17 cm(-1)). The structure of a previously reported iron(III) chloranilate, [Fe-2(C6Cl2O4)(3)(H2O)(4)]. 4H(2)O, has been determined by single crystal X-ray diffraction, revealing a dinuclear structure with one bridging chloranilate, two cis water ligands and one chelating, "terminal" chloranilate per iron(III) centre. [References: 26]
机译:铁(III)离子与氯苯甲酸(2,5-二氯-3,6-二羟基环己-2,5-二烯-1,4-二酮)在空气中的热溶液中反应生成的产物中,令人惊讶地,如结构,磁性和莫斯鲍尔光谱研究所示,其处于+ II氧化态。组成[Fe(C6Cl2O4)(H2O)(2)]产物的单晶X射线研究。 H2O揭示了一维之字形聚合物结构,其中铁(II)离子带有两个顺式氯配体,它们通过桥接氯酸根阴离子连接在一起。晶格水和链之间的氢键结合以及相邻链中C6Cl2单元的紧密堆积,形成了非常紧凑的3维网络。相同的产物可以直接由铁离子生成。观察到J = + 0.47 cm(-1)的高自旋铁(II)中心之间的弱铁磁耦合。可以得到同构结晶材料,其中Fe-II被Mn-II,Zn-II和Cd-II取代,在后一种情况下进行了完整的结构改进。在锰的情况下(J = -0.17 cm(-1)),在高自旋金属中心之间观察到非常弱的反铁磁耦合。先前报道的三价氯苯甲酸铁([Fe-2(C6Cl2O4)(3)(H2O)(4)]的结构。通过单晶X射线衍射测定了4H(2)O,揭示了一种双核结构,每个铁(III)中心具有一个桥接的氯苯甲酸酯,两个顺式水配体和一个螯合的“末端”氯苯甲酸酯。 [参考:26]

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