School of Chemistry, University of Southampton, Southampton, SO17 1BJ, UK.
Chemistry. 2009 Nov 9;15(44):11928-36. doi: 10.1002/chem.200901135.
Glassy carbon electrodes functionalised with two redox centres have been prepared by using electrochemical and solid-phase synthetic methodologies. Initially the individual coupling of anthraquinone, nitrobenzene and dihydroxybenzene to a glassy carbon electrode bearing an ethylenediamine linker was optimised by using different coupling agents and conditions. Bifunctionalisation was then carried out, either simultaneously, with a mixture of nitrobenzene and dihydroxybenzene, or sequentially, with anthraquinone then nitrobenzene and with anthraquinone then dihydroxybenzene. Characterisation of these electrodes by cyclic voltammetry and differential pulse voltammetry clearly proved the attachment of the pairs of redox centres to the glassy carbon electrode. Their partial surface coverages can be controlled by varying the coupling agent or by controlling the substrate concentration during the solid-phase coupling process. Trifunctionalisation was also realised according to this methodology.
通过电化学和固相合成方法制备了两种氧化还原中心功能化的玻碳电极。首先,通过使用不同的偶联剂和条件,优化了蒽醌、硝基苯和二羟基苯分别偶联到带有乙二胺连接体的玻碳电极上的过程。然后进行了双官能化,或者同时使用硝基苯和二羟基苯的混合物进行,或者顺序进行,先将蒽醌与硝基苯偶联,然后再与二羟基苯偶联。通过循环伏安法和差分脉冲伏安法对这些电极进行的表征清楚地证明了氧化还原中心对玻碳电极的附着。通过改变偶联剂或控制固相偶联过程中的底物浓度,可以控制它们的部分表面覆盖率。根据该方法还实现了三官能化。