...
首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Tetrapodal amidoxime ligands I. Coordination isomerism due to self-complementary dimerization of a pyramidal cobalt(iii) coordination module
【24h】

Tetrapodal amidoxime ligands I. Coordination isomerism due to self-complementary dimerization of a pyramidal cobalt(iii) coordination module

机译:四足型a胺肟配体I.金字塔形钴(iii)配位模块自互补二聚化导致的配位异构

获取原文
获取原文并翻译 | 示例
           

摘要

A bis-μ-amidoximato-bridged cobalt(iii) dimer obtained with a new tetrapodal ligand possesses interesting structural parameters as a consequence of intramolecular hydrogen bonding intentionally built into the complex. Its synthesis and properties are described. The new ligand type combines attributes of two previously described ligand classes: It binds a metal ion in a tetrapodal pentadentate fashion and forms a pseudomacrocycle through hydrogen bonds, characteristic of chelating oxime ligands. Coordination isomerism, which is a consequence of dimer formation, has been analyzed by means of X-ray crystallography and carbon-13 nuclear magnetic resonance spectroscopy.
机译:通过新的四足配体获得的双-μ-酰胺基桥接的钴(iii)二聚体具有有趣的结构参数,这是由于分子内氢键故意内置在配合物中。描述了其合成和性质。新的配体类型结合了先前描述的两种配体类型的属性:它以四足五极体的形式结合金属离子,并通过氢键形成螯合肟配体的特征的假大环。由于二聚体形成的结果,配位异构现象已经通过X射线晶体学和碳13核磁共振光谱法进行了分析。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号