Laboratoire de Catalyse en Chimie Organique, Equipe Electrocatalyse, UMR 6503 CNRS Université de Poitiers, 40 Avenue du Recteur Pineau, F-86022 Poitiers Cedex, France.
Langmuir. 2010 Sep 21;26(18):15002-9. doi: 10.1021/la1024313.
Different carbon materials were modified using iodonium ion reduction creating radicals, which after reaction with carbon surfaces formed grafted layers of molecules. Several molecules (4-bromophenyl, 4-fluorophenyl, 6-chlorohexyne, and 4-bromobutyne) were grafted on glassy carbon and Vulcan XC72 carbon substrates. Carbon substrates were shown to be free of halogen atoms; therefore, the quantification of the grafted groups containing halogen atoms was facilitated. The grafting of the different molecules was first electrochemically studied on glassy carbon electrodes using cyclic voltammetry, in order to determine the reduction potential of the corresponding iodonium ions. Voltammetric study using Fe(CN)(6)(4-) and Fe(CN)(6)(3-) probe molecules and XPS characterization were also used to evidence the effectiveness of grafting from iodonium ion reduction reaction. Reduction potentials were found in the range from -0.9 V vs SCE to -1.0 V vs SCE, lower than those for corresponding diazonium ion reduction reaction on glassy carbon (close to -0.3 V vs SCE). Therefore, grafted layers from iodonium ions were carried out on carbon Vulcan XC72 powder using NaBH(4) as reducing agent. Functionalized carbon powders were characterized by elemental analysis, thermogravimetric analysis, and X-ray photoelectron spectroscopy to evidence the presence of grafted molecules on the materials. However, low grafting yields were obtained. Then, several synthesis parameters were studied to optimize the grafting reactions, such as the control of the addition of reactants and their concentrations, leading to increase the surface concentration by a factor 2. At last, according to XPS measurements the grafting of alkinyliodonium ions led to very low surface concentrations (0.5 wt % for 6-chlorohexyne), whereas elemental analysis and TGA indicate ca. 2.4 wt % and ca. 5 wt %, respectively.
不同的碳材料经过碘翁离子还原生成自由基修饰后,与碳表面反应形成接枝分子层。几种分子(4-溴苯基、4-氟苯基、6-氯己炔和 4-溴丁炔)被接枝到玻璃碳和 Vulcan XC72 碳基底上。由于碳基底不含卤原子,因此可以方便地对含卤原子的接枝基团进行定量分析。首先通过循环伏安法在玻璃碳电极上电化学研究了不同分子的接枝,以确定相应的碘翁离子的还原电位。还使用 Fe(CN)(6)(4-)和 Fe(CN)(6)(3-)探针分子的伏安法研究和 XPS 表征来证明碘翁离子还原反应接枝的有效性。还原电位的范围为-0.9 V 至-1.0 V(相对于 SCE),低于相应的玻璃碳上的重氮离子还原反应(接近-0.3 V 相对于 SCE)。因此,使用硼氢化钠作为还原剂在 Vulcan XC72 碳粉末上进行碘翁离子接枝。通过元素分析、热重分析和 X 射线光电子能谱对功能化碳粉进行了表征,以证明材料上存在接枝分子。然而,接枝产率较低。然后,研究了几个合成参数来优化接枝反应,例如控制反应物的添加及其浓度,从而使表面浓度提高了 2 倍。最后,根据 XPS 测量结果,炔基碘翁离子的接枝导致表面浓度非常低(6-氯己炔为 0.5wt%),而元素分析和 TGA 分别表明约为 2.4wt%和 5wt%。