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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Synthesis and characterization of nona- and trideca-nuclear manganese phosphonate clusters
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Synthesis and characterization of nona- and trideca-nuclear manganese phosphonate clusters

机译:九核和十三核磷酸膦酸锰团簇的合成与表征

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Two new Mn(III) complexes with unprecedented topologies containing the tert-butylphosphonate ligand (t-BuPO32-), [Mn9O6(t-BuPO3)(2)(O2CMe)(11)(MeCOOH)(H2O)] center dot 8H(2)O (1), and [NBu4n][Mn13O6(t-BuPO3)(10)(OH)(2)(N-3)(6)(MeCOOH)(2)(H2O)(2)] center dot 6H(2)O (2) have been prepared by treatment of Mn(O2CMe)(2) and (NBu4MnO4)-Mn-n with tert-butylphosphonic acid in the presence of different bases. The core of 1 consists of two [Mn3O] units connected to a near linear [Mn-3] unit by four mu(3)-O, while the core of 2 possesses a Mn centred disklike [Mn7O6] unit linked to six additional manganese atoms via six mu(4)-O. Compounds 1 and 2 are both homovalent manganese(III) cage clusters, of which the six-coordinated Mn centers are all Jahn-Teller distorted. Magnetic susceptibility measurements reveal that compounds 1 and 2 display overall ferromagnetic and antiferromagnetic interactions, respectively, between the adjacent Mn-III ions. Both the in-phase signal chi'T-M and out-of-phase signal chi ''(M) of the two complexes exhibit frequency-dependence below approximately 3 K.
机译:两个具有前所未有拓扑结构的新型Mn(III)配合物,其中包含叔丁基膦酸酯配体(t-BuPO32-),[Mn9O6(t-BuPO3)(2)(O2CMe)(11)(MeCOOH)(H2O)]中心点8H( 2)O(1)和[NBu4n] [Mn13O6(t-BuPO3)(10)(OH)(2)(N-3)(6)(MeCOOH)(2)(H2O)(2)]中心点在不同的碱存在下,用叔丁基膦酸处理Mn(O2CMe)(2)和(NBu4MnO4)-Mn-n可制得6H(2)O(2)。 1的核心由两个[Mn3O]单元组成,它们通过四个mu(3)-O连接到接近线性的[Mn-3]单元,而2的核心具有一个与六个附加锰连接的Mn中心盘状[Mn7O6]单元通过六个mu(4)-O原子。化合物1和2均为同价锰(III)笼形簇,其中六个配位的Mn中心均被Jahn-Teller扭曲。磁化率测量表明,化合物1和2在相邻的Mn-III离子之间分别显示总体铁磁和反铁磁相互作用。两个复合物的同相信号chi'T-M和异相信号chi''(M)都显示出大约3 K以下的频率相关性。

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