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首页> 外文期刊>Electrochimica Acta >Electrochemistry of icosahedral cobalt bis(dicarbollide) ions and their carbon and boron substituted derivatives in aqueous phosphate buffers
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Electrochemistry of icosahedral cobalt bis(dicarbollide) ions and their carbon and boron substituted derivatives in aqueous phosphate buffers

机译:磷酸乙二圆体钴双(二碳丙酰基)离子和碳酸碳和硼取代衍生物在磷酸盐缓冲液中的电化学

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Herein we present investigations of electrochemical behavior over a series of selected bisicosahedral cobalt bis(heteroborane)(1-) derivatives in aqueous phosphate buffers. This pilot study is focused on distinct effects connected with either exo-skeletal substitutions at boron atoms with bridging and nonbridging groups or by influence of endo-hedral replacement of four cage CH groups present in the parent cobalt bis(dicarbollide) ion by two isolobal sulfur groups. The substitutions can thus be utilized for an easy tuning of the electrochemical properties of these boron polyhedral ions and for optimizing their responses in two quite broad electrochemical windows. The former is found in the negative potential corresponding to the redox process on the central metal atom; the latter, which was not considered in the literature, is located in the positive potential region and is connected with core cage oxidation process. Such properties seem to provide promising potential for electroanalytical sensing of this family of heterometallaboranes in tissues and their use for electrolabelling of biopolymers. (C) 2020 Elsevier Ltd. All rights reserved.
机译:在此,我们在磷酸水溶液中的一系列选定的双孢菌钴双(异硼烷)(1-)衍生物上的电化学行为的研究。该试点研究重点关注与硼原子的外骨骨级取代与桥接和非录制组连接的不同作用,或者通过两只孤立硫磺硫磺含有母钴双(二羰基团)离子中存在的四个笼子Ch组的肠海丘替代团体。因此,取代可以用于容易调整这些硼多面体离子的电化学性质,并优化其在两个相当宽的电化学窗口中的反应。前者在与中央金属原子上的氧化还原过程相对应的负电位中发现;在文献中未考虑的后者位于正电位区域,并与核心笼氧化过程连接。这种性质似乎为该杂种算子在组织中的杂种硅烷织物的电催化感测的有希望的潜力及其用于生物聚合物的电解的用途。 (c)2020 elestvier有限公司保留所有权利。

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