首页> 外文期刊>Inorganica Chimica Acta >Organoosmium complexes of imidazole-containing chelate acceptor ligands
【24h】

Organoosmium complexes of imidazole-containing chelate acceptor ligands

机译:含咪唑螯合物受体配体的有机oo配合物

获取原文
获取原文并翻译 | 示例
           

摘要

The complexes [(L)Os(η~6-Cym)Cl](PF_6), Cym = p-cymene and L = bis(1-methylimidazol-2-yl)ketone (bik) or bis(1-methylimidazol- 2-yl)glyoxal (big), were obtained and characterized with respect to spectroscopy, crystal structure (big complex) and (spectro)electrochemical behaviour at variable temperatures. DFT calculations confirm the structure of [(big)Os(η~6-Cym)Cl]~+ with imidazolyl-N-bonded Os ~(II) in a boat-shaped seven-membered chelate ring with small N-Os-N angles (<84°). Reduction of this compound proceeds reversibly to a neutral complex of the α-semidione radical anion ligand big~-; EPR and IR spectroelectrochemistry indicate very little participation from the heavy metal in the spin distribution. The analogous [(bik)Os(η~6- Cym)Cl]~+ could not be reduced reversibly to the ketyl radical complex but displayed a more reversible oxidation at high potential.
机译:配合物[(L)Os(η〜6-Cym)Cl](PF_6),Cym =对异丙基,L =双(1-甲基咪唑-2-基)酮(bik)或双(1-甲基咪唑-2)得到-(基)乙二醛(大),并在可变温度下的光谱,晶体结构(大配合物)和(光谱)电化学行为方面进行了表征。 DFT计算证实了在具有小N-Os-N的船形七元螯合环中具有咪唑基-N键合的Os〜(II)的[(大)Os(η〜6-Cym)Cl]〜+的结构。角度(<84°)。该化合物的还原可逆地进行至α-半二酮自由基阴离子配体big--的中性络合物。 EPR和IR光谱电化学表明,重金属很少参与自旋分布。相似的[(bik)Os(η〜6- Cym)Cl]〜+不能可逆地还原为酮基自由基络合物,但在高电势下表现出更可逆的氧化作用。

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