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双-[4-(二甲基氨基)吡啶鎓]四-(硫氰酸根-κ)锰(II)和三-[4-(二甲基氨基)吡啶鎓]五-(硫氰酸根-κ)锰(II)的晶体结构

Crystal structures of bis-[4-(di-methyl-amino)-pyridinium] tetra-kis-(thio-cyanato-κ)manganate(II) and tris-[4-(di-methyl-amino)-pyridinium] penta-kis(thio-cyanato-κ)manganate(II).

作者信息

Neumann Tristan, Jess Inke, Näther Christian

机构信息

Institut für Anorganische Chemie, Christian-Albrechts-Universität Kiel, Max-Eyth Strasse 2, D-24118 Kiel, Germany.

出版信息

Acta Crystallogr E Crystallogr Commun. 2018 Jan 1;74(Pt 1):15-20. doi: 10.1107/S2056989017017510.

Abstract

The crystal structures of the title salts, (CHN)[Mn(NCS)] () and (CHN)[Mn(NCS)] (), consist of manganese(II) cations that are tetra-hedrally () or trigonal-bipyramidally () coordinated to four or five terminal N-bonded thio-cyanate ligands, respectively, into discrete anionic complexes. The negative charge is compensated by two () or three () 4-(di-methyl-amino)-pyridinium cations, which are protonated at the pyridine N atom. The asymmetric unit of compound consists of one anionic complex and two 4-(di-methyl-amino)-pyridinium cations, whereas that of compound consists of two anionic complexes and six 4-(di-methyl-amino)-pyridinium cations, all of them located in general positions. These complexes are linked by N-H⋯S, C-H⋯S and C-H⋯N hydrogen-bonding inter-actions between the 4-(di-methyl-amino)-pyridinium cations and the thio-cyanate ligands into three-dimensional network structures.

摘要

标题盐(CHN)[Mn(NCS)]()和(CHN)[Mn(NCS)]()的晶体结构由锰(II)阳离子组成,这些阳离子分别以四面体()或三角双锥()方式与四个或五个末端N键合的硫氰酸酯配体配位,形成离散的阴离子配合物。负电荷由两个()或三个()4-(二甲基氨基)吡啶鎓阳离子补偿,这些阳离子在吡啶N原子处质子化。化合物的不对称单元由一个阴离子配合物和两个4-(二甲基氨基)吡啶鎓阳离子组成,而化合物的不对称单元由两个阴离子配合物和六个4-(二甲基氨基)吡啶鎓阳离子组成,它们都位于一般位置。这些配合物通过4-(二甲基氨基)吡啶鎓阳离子与硫氰酸酯配体之间的N-H⋯S、C-H⋯S和C-H⋯N氢键相互作用连接成三维网络结构。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d770/5778477/c6d27acc8211/e-74-00015-fig1.jpg

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