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双(乙醇-κO)双-(吡啶-3-甲醛-κN硫代半卡巴腙)双-(硫氰酸根合-κN)铁(II)-吡啶-3-甲醛硫代半卡巴腙(1/2)

Bis(ethanol-κO)bis-(pyridine-3-carb-aldehyde-κN thio-semicarbazone)bis-(thio-cyanato-κN)iron(II)-pyridine-3-carbaldehyde thio-semicarbazone (1/2).

作者信息

Wang Shao-Mei

机构信息

College of Chemistry and Chemical Engineering, Anyang Normal University, Anyang, Henan 455000, People's Republic of China.

出版信息

Acta Crystallogr Sect E Struct Rep Online. 2009 Jul 1;65(Pt 8):m847. doi: 10.1107/S1600536809024076.

DOI:10.1107/S1600536809024076
PMID:21583317
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2977344/
Abstract

The crystal structure of the title Fe(II) complex, [Fe(NCS)(2)(C(7)H(8)N(4)S)(2)(CH(3)CH(2)OH)(2)]·2C(7)H(8)N(4)S, based on the Schiff base ligand pyridine-3-carbaldehyde thio-semicarbazone (pct), results from the cocrystallization of an Fe(II) coordination compound together with two of the pct ligands. The complex unit is mononuclear, with the central Fe(II) ion located on a crystallographic centre of inversion and coordinated by four N atoms from two pct ligands and two thio-cyanate anions. The slightly distorted octa-hedral coordination is completed by two O atoms from ethanol mol-ecules. The crystal packing is accomplished inter-molecular N-H⋯S hydrogen bonds.

摘要

标题为[Fe(NCS)(2)(C(7)H(8)N(4)S)(2)(CH(3)CH(2)OH)(2)]·2C(7)H(8)N(4)S的铁(II)配合物基于席夫碱配体吡啶-3-甲醛硫代半卡巴腙(pct),是由一种铁(II)配位化合物与两个pct配体共结晶得到的。配合物单元为单核,中心铁(II)离子位于一个晶体学反演中心,由来自两个pct配体的四个N原子和两个硫氰酸根阴离子配位。两个乙醇分子的O原子完成了略微扭曲的八面体配位。晶体堆积通过分子间的N-H⋯S氢键实现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbf2/2977344/ae8d8a3d31e9/e-65-0m847-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbf2/2977344/1f13be4bdcb3/e-65-0m847-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbf2/2977344/ae8d8a3d31e9/e-65-0m847-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbf2/2977344/1f13be4bdcb3/e-65-0m847-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbf2/2977344/ae8d8a3d31e9/e-65-0m847-fig2.jpg

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