Crystal structure of octa-kis-(4-meth-oxy-pyridinium) bis-(4-meth-oxy-pyridine-κ N)tetra-kis-(thio-cyanato-κ N)ferrate(III) bis-[(4-meth-oxypyri-dine-κ N)pentakis-(thio-cyanato-κ N)ferrate(III)] hexa-kis-(thio-cyanato-κ N)ferrate(III) with iron in three different octa-hedral coordination environments

八基斯-(4-甲氧基-吡啶鎓)双-(4-甲氧基-吡啶-κ N)四基斯-(硫代氰基-κ N)铁酸盐(III)双-[(4-甲氧基吡啶-κ N)五基-(硫代氰基-κ N)高铁酸盐(III)]六基斯-(硫代氰基-κ N)铁酸盐(III)]的晶体结构N)高铁酸盐(III)与铁在三种不同的八面体配位环境中

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作者:Aleksej Jochim, Inke Jess, Christian Näther

Abstract

The crystal structure of the title salt, (C6H8NO)8[Fe(NCS)4(C6H7NO)2][Fe(NCS)5(C6H7NO)]2[Fe(NCS)6], comprises three negatively charged octa-hedral FeIII complexes with different coordination environments in which the FeIII atoms are coordinated by a different number of thio-cyanate anions and 4-meth-oxy-pyridine ligands. Charge balance is achieved by 4-meth-oxy-pyridinium cations. The asymmetric unit consists of three FeIII cations, one of which is located on a centre of inversion, one on a twofold rotation axis and one in a general position, and ten thio-cyanate anions, two 4-meth-oxy-pyridine ligands and 4-meth-oxy-pyridinium cations (one of which is disordered over two sets of sites). Beside to Coulombic inter-actions between organic cations and the ferrate(III) anions, weak N-H⋯S hydrogen-bonding inter-actions involving the pyridinium N-H groups of the cations and the thio-cyanate S atoms of the complex anions are mainly responsible for the cohesion of the crystal structure.

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