首页> 外文期刊>Journal of the Chemical Society. Dalton Transactions >Electrochemically generated chemiluminescence of tris (2,2 '-bipyridine) ruthenium(II), tris(1,10-phenathroline)ruthenium(II) and tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(II) complexes
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Electrochemically generated chemiluminescence of tris (2,2 '-bipyridine) ruthenium(II), tris(1,10-phenathroline)ruthenium(II) and tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(II) complexes

机译:三(2,2'-联吡啶)钌(II),三(1,10-菲咯啉)钌(II)和三(4,7-二苯基-1,10-菲咯啉)钌(II)络合物的电化学化学发光

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摘要

The electrochemically generated chemiluminescence (ECL) of the title complexes with four series of electroactive organic compounds Q in 0.1 M (C2H5)(4)NPF6 acetonitrile solutions has been studied using a triple-potential-step technique. The yields of the formation of the excited *RuL32+ ion produced by the electron transfer reaction of RuL3+ with aromatic amine or 2,3,7,8-tetramehoxythianthrene radical cations and by the reaction of RuL33+ with quinone or nitroaromatic radical anions as well as with N-methylpyridinium radicals have been determined. A reaction scheme describing generation of the excited *RuL32+ has been comparatively discussed with that for the quenching reactions with conclusion that spin conversion between two spin forms (3)[RuL33+/+...Q(-/+)] and (1)[RuL33+/+...Q(-/+)] of an activated complex play a crucial role in both electron transfer processes. [References: 50]
机译:使用三电位步骤技术研究了在0.1 M(C2H5)(4)NPF6乙腈溶液中具有四个系列电活性有机化合物Q的标题配合物的电化学生成化学发光(ECL)。通过RuL3 +与芳族胺或2,3,7,8-四甲氧基噻吨基阳离子的电子转移反应以及RuL33 +与醌或硝基芳族自由基阴离子以及与之反应生成的激发* RuL32 +离子已经确定了N-甲基吡啶鎓基团。已经比较讨论了描述激发* RuL32 +生成的反应方案和淬灭反应的方案,得出的结论是两种自旋形式(3)[RuL33 + / + ... Q(-/ +)]和(1)之间的自旋转化活化的配合物的[RuL33 + / + ... Q(-/ +)]在两个电子转移过程中都起着至关重要的作用。 [参考:50]

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