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首页> 外文期刊>Zeitschrift fur Anorganische und Allgemeine Chemie >Synthesis, Crystal Structures, and Properties of Mn(NCS)_2 Coordination Compounds with 4-Picoline as Coligand and Crystal Structure of Mn(NCS)_2
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Synthesis, Crystal Structures, and Properties of Mn(NCS)_2 Coordination Compounds with 4-Picoline as Coligand and Crystal Structure of Mn(NCS)_2

机译:用4-巯基的Mn(NCS)_2配位化合物的合成,晶体结构和性质与Mn(NCS)的COLIGAND和晶体结构_2

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摘要

Reaction of Mn(NCS)_2 with 4-picoline (4-methylpyridine) leads to the formation of [Mn(NCS)_2(4-picoline)4]·0.67·4-picoline· 0.33·H_2O (1-Mn) reported in literature, Mn(NCS)_2(4-picoline)2(H2O)2 (2-Mn/H2O), and of [Mn(NCS)_2(4-picoline)2]n (2-Mn/I). 1-Mn and 2-Mn/H_2O consist of discrete complexes, in which the metal cations are octahedrally coordinated, whereas in 2-Mn/I the metal cations are linked by pairs of μ-1,3-bridging thiocyanate anions into corrugated chains. Measurements using thermogravimetry and differential scanning calorimetry as well as temperature dependent X-ray powder diffraction on 1-Mn and 2-Mn/H_2O reveal that upon heating both compounds transform into [Mn(NCS)_2(4-picoline)]n (3-Mn) via 2-Mn/I as intermediate. 3-Mn shows a very rare chain topology in which the metal cations are linked by μ-1,3,3 (N,S,S) coordinating anionic ligands which was never observed before with MnII. From these investigations there is no hint that a further modification of 2-Mn can be prepared as recently observed for [M(NCS)_2(4-picoline)2]n (M = Fe, Cd) and such a form is also not available if the metastable forms of the FeII or CdII compounds were used as template during thermal decomposition. Magnetic investigations on 2-Mn/H_2O show only paramagnetic behavior, whereas for 2-Mn/I antiferromagnetic ordering is observed. Finally, the crystal structure of Mn(NCS)_2 was determined from XRPD data, which shows that it is strongly related to that of 3-Mn.
机译:Mn(NCS)_2与4-吡啶(4-甲基吡啶)的反应导致[Mn(NCS)_2(4-吡啶)4]·0.67·4-吡啶·0.33·H_2O(1-MN)的形成在文献中,Mn(NCS)_2(4-吡啶)2(H 2 O)2(2-Mn / H 2 O)和[Mn(NCS)_2(4-吡啶)2] N(2-Mn / I)。由离散复合物组成,其中金属阳离子是八面体配位的离散复合物组成,而在2-Mn / I中,金属阳离子通过对μ-1,3-桥接硫氰酸盐阴离子与瓦楞链连接。使用热重率和差示扫描量热法的测量以及1-Mn和2-Mn / h_2o上的温度依赖性X射线粉末衍射显示,在将两种化合物加热到[Mn(ncs)_2(4-吡啶)] n(3 -mn)通过2-mn / i作为中间体。 3-MN显示了一种非常稀有的链拓扑,其中金属阳离子通过μ-1,3,3(N,S,S)连接的阴离子配体连接,所述阴离子配体从未观察到以前没有观察到的MNII。从这些调查中,没有暗示可以制备2-Mn的进一步修饰,如最近观察到[m(ncs)_2(4-吡啶)2] n(m = Fe,Cd),这种形式也没有如果在热分解期间使用FeII或CDII化合物的亚硫化合物的亚硫或CDII化合物的形式可用。 2-Mn / H_2O上的磁性研究仅展示了顺磁性行为,而观察到2mN / I抗铁磁性排序。最后,从XRPD数据确定Mn(NCS)_2的晶体结构,表明它与3-Mn的强烈相关。

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