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首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >Mixed 3d/4d and 3d/4f metal clusters: Tetranuclear (Fe2M2III)-M-III (M-III = Ln, Y) and (Mn2M2III)-M-IV (M = Yb, Y) complexes, and the first Fe/4f single-molecule magnets
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Mixed 3d/4d and 3d/4f metal clusters: Tetranuclear (Fe2M2III)-M-III (M-III = Ln, Y) and (Mn2M2III)-M-IV (M = Yb, Y) complexes, and the first Fe/4f single-molecule magnets

机译:混合的3d / 4d和3d / 4f金属簇:四核(Fe2M2III)-M-III(M-III = Ln,Y)和(Mn2M2III)-M-IV(M = Yb,Y)配合物,以及第一个Fe / 4f单分子磁体

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The synthesis, structure and magnetic properties are reported of Fe(2)Ln(2), Fe2Y2, Mn2Yb2 and Mn2Y2 complexes. The compound [Fe2Ho2(OH)(2)(teaH)(2)(O2CPh)(4)(NO3)(2)] (1), where teaH(3) is triethanolamine, was obtained from the reaction of eight equivalents of teaH(3) with one equivalent each of Ho(NO3)(3) and [Fe3O(O2CPh)(6)(H2O)(3)](O2CPh) in MeCN/MeOH. The use instead of Dy(NO3)(3) or Tb(NO3)(3) leads to the structurally similar products [Fe2Dy2(OH)(2)(teaH)(2)(O2CPh)(6)] (2) and [Fe2Tb2(OH)(2)(teaH)(2)(O2CPh)(6)] (3). The compounds [Fe2Y2(pdmH)(6)Cl-4]Cl-2 (4) and isostructural [Fe2Ho2(pdmH)(6)Cl-4]Cl-2 (5), where pdmH(2) is pyridine-2,6-dimethanol, were prepared from the reaction of four equivalents of pdmH(2) with two equivalents of YCl3 or HoCl3, respectively, and FeCl2 in MeOH. The compounds [Mn2Y2O2(O2CPh)(6)(OMe)(4)(MeOH)(4)] (6) and [Mn2Yb2O2(O2CPh)(6)(OMe)(4)(MeOH)(4)] (7) were prepared by methanolysis of (NBu4n)-[Mn4O2(O2CPh)(9)(H2O)] in the presence of Yb(NO3)(3) or Y(NO3)(3), respectively. Complexes 1-3, 6 and 7 contain a 'defect dicubane' M-4 core (including the first mixed 3d/4f examples of this type to contain Fe-III or Mn-IV), whereas 4 and 5 have a U-shaped core. Variable-temperature solid-state magnetic susceptibility studies of 1-6 in the temperature range 5.00-300 K were carried out, and for all the complexes predominantly antiferromagnetic exchange interactions between the metal centers was observed. Magnetization versus applied field sweeps on single crystals of 1 and 2 at low temperature reveal hysteresis loops, confirming these species to be new examples of single-molecule magnets (SMMs). Thus, complexes I and 2 are the first examples of Fe/4f SMMS. (c) 2005 Elsevier Ltd. All rights reserved.
机译:报道了Fe(2)Ln(2),Fe2Y2,Mn2Yb2和Mn2Y2配合物的合成,结构和磁性。化合物[Fe2Ho2(OH)(2)(teaH)(2)(O2CPh)(4)(NO3)(2)](1)(其中teaH(3)为三乙醇胺)是由八当量的teaH(3),其中每当量的Ho(NO3)(3)和[Fe3O(O2CPh)(6)(H2O)(3)](O2CPh)均在MeCN / MeOH中。代替Dy(NO3)(3)或Tb(NO3)(3)的使用会导致结构相似的产品[Fe2Dy2(OH)(2)(teaH)(2)(O2CPh)(6)](2)和[Fe 2 Tb 2(OH)(2)(teaH)(2)(O 2 CPh)(6)](3)。化合物[Fe2Y2(pdmH)(6)Cl-4] Cl-2(4)和同结构的[Fe2Ho2(pdmH)(6)Cl-4] Cl-2(5),其中pdmH(2)为吡啶-2由四当量的pdmH(2)与两当量的YCl3或HoCl3以及FeCl2在MeOH中的反应制得1,6-二甲醇。化合物[Mn2Y2O2(O2CPh)(6)(OMe)(4)(MeOH)(4)](6)和[Mn2Yb2O2(O2CPh)(6)(OMe)(4)(MeOH)(4)](7 )是分别在Yb(NO3)(3)或Y(NO3)(3)存在下通过甲醇分解(NBu4n)-[Mn4O2(O2CPh)(9)(H2O)]制备的。配合物1-3、6和7包含一个“缺陷孵化器” M-4核(包括第一个混合的3d / 4f此类例子,其中包含Fe-III或Mn-IV),而4和5则呈U形核心。在5.00-300 K的温度范围内进行了1-6的可变温度固态磁化率研究,发现对于所有配合物,主要观察到金属中心之间的反铁磁交换相互作用。低温下在1和2的单晶上的磁化与施加的场扫描显示出磁滞回线,证实了这些物种是单分子磁体(SMM)的新实例。因此,配合物I和2是Fe / 4f SMMS的第一个例子。 (c)2005 Elsevier Ltd.保留所有权利。

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