Electrochemically assisted grafting of asymmetric alkynyl(aryl)iodonium salts on glassy carbon with focus on the alkynyl/aryl grafting ratio

被引:7
作者
Florini, Nicola [1 ]
Michelazzi, Marco [1 ]
Parenti, Francesca [1 ]
Mucci, Adele [1 ]
Sola, Marco [1 ]
Baratti, Carla [2 ]
De Renzi, Valentina [2 ]
Daasbjerg, Kim [3 ]
Pedersen, Steen Uttrup [3 ]
Fontanesi, Claudio [1 ]
机构
[1] Univ Modena, Dept Chem, I-41100 Modena, Italy
[2] Univ Modena, Dept Phys, I-41100 Modena, Italy
[3] Aarhus Univ, Dept Chem, DK-8000 Aarhus, Denmark
关键词
Grafting; Iodonium salt; DFT; DIAZONIUM SALTS; COVALENT MODIFICATION; EPOXY COMPOSITES; ORGANIC LAYERS; FIBER SURFACES; REDUCTION; ARYL; ELECTRODES; RADICALS; DERIVATIZATION;
D O I
10.1016/j.jelechem.2013.01.023
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Glassy carbon (GC) surfaces are functionalized exploiting the electrochemical reduction of asymmetric iodonium salts of the general formula [4-Z-C6H4-I+-C=C(CH2)(4)Cl, Z = NO2, Br, F, H, or CH3]. The range of Z groups was selected aiming to examine the C-aryl-I bond energy as a function of the "electron withdrawing/electron donating" ability of the Z-group, with the ultimate purpose of controlling the alkynyl/aryl grafting ratio. The electroreduction mechanism and the characteristics of the grafted surface are studied by means of cyclic voltammetry and X-ray photoelectron spectroscopy. It is shown that the alkynyl/aryl grafting ratio decreases with the increasing electron withdrawing nature of Z, which induces a weakening of the C-aryl-I bond. Ab initio DFT vertical electron affinities (EA(v)) allowed to rationalize the electroreduction potentials of both the bulk and surface functionalised redox couples. Moreover, the alkynyl/aryl grafting ratio is assessed, at a molecular level, on the basis of ab initio DFT potential energy surfaces. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:41 / 47
页数:7
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