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三水合-(7-氧杂双环-[2.2.1]庚烷-2,3-二羧酸根-κO,O,O)钴(II)一水合物

Triaqua-(7-oxabicyclo-[2.2.1]heptane-2,3-dicarboxyl-ato-κO,O,O)cobalt(II) monohydrate.

作者信息

Zhang Fan, Jia Ai-Ping, Lin Qiu-Yue

出版信息

Acta Crystallogr Sect E Struct Rep Online. 2011 Aug 1;67(Pt 8):m1119-20. doi: 10.1107/S1600536811028431. Epub 2011 Jul 23.

DOI:10.1107/S1600536811028431
PMID:22090887
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3212185/
Abstract

The title complex, [Co(C(8)H(8)O(5))(H(2)O)(3)]·H(2)O, was synthesized by reaction of cobalt acetate with 7-oxabicyclo-[2.2.1]heptane-2,3-dicarb-oxy-lic anhydride (norcantharidin) in aqueous solution. In the mol-ecule, the Co(II) atom is six-coordinated in a distorted octa-hedral environment, binding to the bridging O atom of the bicyclo-heptane unit, to two O atoms from monodentate carboxyl-ate groups and to three water O atoms. The crystal structure is stabilized by several O-H⋯O hydrogen-bonding inter-actions involving both the coordinated and uncoordinated water mol-ecules as donors and the carboxyl-ate O atoms of neighbouring mol-ecules as acceptors.

摘要

标题配合物[Co(C₈H₈O₅)(H₂O)₃]·H₂O是通过醋酸钴与7-氧杂双环-[2.2.1]庚烷-2,3-二羧酸酐(去甲斑蝥素)在水溶液中反应合成的。在分子中,Co(II)原子在扭曲的八面体环境中呈六配位,与双环庚烷单元的桥连O原子、来自单齿羧酸根基团的两个O原子以及三个水分子的O原子配位。晶体结构通过几种O-H⋯O氢键相互作用得以稳定,其中配位和未配位的水分子作为供体,相邻分子的羧酸根O原子作为受体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b114/3212185/79740edc6656/e-67-m1119-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b114/3212185/79740edc6656/e-67-m1119-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b114/3212185/79740edc6656/e-67-m1119-fig1.jpg

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