首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Electronic and photophysical properties of a novel phenol bound dinuclear ruthenium complex: evidence for a luminescent mixed valence state
【24h】

Electronic and photophysical properties of a novel phenol bound dinuclear ruthenium complex: evidence for a luminescent mixed valence state

机译:新型酚键合双核钌配合物的电子和光物理性质:发光混合价态的证据

获取原文
获取原文并翻译 | 示例
           

摘要

A novel dinuclear ruthenium(II) complex bridged by dianionic bridge 3-(2-phenol)-5-(pyridin-2-yl)-1,2,4-triazole in which the ruthenium metal atoms are bound through N,N coordination to the pyridine and triazole and O,N coordination to the triazole and phenolate is described. The electrochemical, spectroscopic and photophysical behaviour of the dimer is compared with its associated N,N- and O,N-coordinated mononuclear complexes. The mixed valence complex was prepared electrochemically and a weak inter-valence charge transfer transition is observed which from Hush theory provides an electronic coupling matrix element of 666 cm~(-1), suggesting the complex is weakly coupled and valence trapped. In its native state the dinuclear compound is essentially non-emissive but upon the oxidation of the O,N moiety luminescence from the complex is reversibly switched on at 0.3 V and reversibly switched off by application of 1.3 or 0 V. To our knowledge this is the first report of a luminescent mixed valence ruthenium complex.
机译:通过双阴离子桥3-(2-苯酚)-5-(吡啶-2-基)-1,2,4-三唑桥接的新型双核钌(II)络合物,其中钌金属原子通过N,N配位键结合描述了吡啶和三唑的O,N与三唑和酚盐的O,N配位。将二聚体的电化学,光谱和光物理行为与其相关的N,N和O,N配位的单核络合物进行了比较。用电化学方法制备了混合价态配合物,观察到弱的价间电荷转移跃迁,根据Hush理论,该电子提供了666 cm〜(-1)的电子耦合矩阵元素,表明该配合物弱耦合且能被捕获。在其天然状态下,双核化合物基本上是非发射性的,但在O,N部分被氧化后,复合物的发光在0.3 V时可逆地开启,而在施加1.3或0 V时可逆地关闭。发光混合价钌配合物的首次报道。

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