The electro-oxidation of water and alcohols at BDD in hexafluoroisopropanol

被引:19
作者
Ayata, Sevda [1 ,2 ]
Stefanova, Ana [1 ]
Ernst, Siegfried [1 ]
Baltruschat, Helmut [1 ]
机构
[1] Univ Bonn, Inst Phys & Theoret Chem, D-53117 Bonn, Germany
[2] Dokuz Eylul Univ, Fac Sci, Dept Chem, TR-35160 Izmir, Turkey
关键词
Boron doped diamond; Nonaqueous electrolyte; HFIP; Rotating ring disc electrode; DOPED DIAMOND ELECTRODES; FLUORINATED ALCOHOLS; HYDROGEN-PEROXIDE; OLEFIN EPOXIDATION; HYDROXYL RADICALS; COUPLING REACTION; AQUEOUS-SOLUTION; OXIDATION; SOLVENTS; ELECTROCHEMISTRY;
D O I
10.1016/j.jelechem.2013.03.024
中图分类号
O65 [分析化学];
学科分类号
070302 [分析化学];
摘要
Boron doped (BDD) diamond electrodes have a wide potential window and thus allow the formation of radicals and the investigation of their reactions. Hexafluoroisopropanol is able to extend greatly the lifetime of radical cations. Here, we investigated the oxidation of a series of the hydroxyl containing species at a BDD electrode in that solvent: water and the simplest primary, secondary, and tertiary alcohols, i.e. methanol, i-propanol, and t-butanol. The ease of their oxidation does not follow the hydrogen basicity but rather the bond dissociation energy. The radicals formed from water, methanol, and i-propanol are very short-lived and we can detect electrochemically only the second reaction product, i.e. the hydrogen ions. In contrast, t-butanol is oxidised to an intermediate, which is transformed much more slowly within some seconds to another species. This species can be further oxidised more easily than the first intermediate or the initial reactant. There is some evidence, that the reactant molecules play a dual role: on the one hand they undergo oxidative hydrogen abstraction. On the other hand, they stabilise the produced hydrogen ions. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 6
页数:6
相关论文
共 32 条
[1]
[Anonymous], 2001, ELECTROCHEMICAL METH
[2]
Asmus K.D., 1987, J CHEM SOC CHEM COMM, P208
[3]
PULSE RADIOLYTIC STUDY OF SITE OF OH RADICAL ATTACK ON ALIPHATIC ALCOHOLS IN AQUEOUS-SOLUTION [J].
ASMUS, KD ;
MOCKEL, H ;
HENGLEIN, A .
JOURNAL OF PHYSICAL CHEMISTRY, 1973, 77 (10) :1218-1221
[4]
Kinetic studies of olefin epoxidation with hydrogen peroxide in 1,1,1,3,3,3-hexafluoro-2-propanol reveal a crucial catalytic role for solvent clusters [J].
Berkessel, A ;
Adrio, JA .
ADVANCED SYNTHESIS & CATALYSIS, 2004, 346 (2-3) :275-280
[5]
Dramatic acceleration of olefin epoxidation in fluorinated alcohols: Activation of hydrogen peroxide by multiple H-bond networks [J].
Berkessel, Albrecht ;
Adrio, Jens A. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (41) :13412-13420
[6]
Unveiling the "booster effect" of fluorinated alcohol solvents:: Aggregation-induced conformational changes and cooperatively enhanced H-bonding [J].
Berkessel, Albrecht ;
Adrio, Jens A. ;
Huettenhain, Daniel ;
Neudoerfl, Jorg M. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (26) :8421-8426
[7]
Kinetic isotope effect for hydrogen abstraction by •OH radicals from normal and carbon-deuterated ethyl alcohol and methylamine in aqueous solutions [J].
Bonifacic, M ;
Armstrong, DA ;
Stefanic, I ;
Asmus, KD .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (30) :7268-7276
[8]
1,1,1,3,3,3-hexafluoropropan-2-ol (HFP) as a solvent for electrochemistry [J].
Eberson, L ;
Hartshorn, MP ;
McCullough, JJ ;
Persson, O ;
Radner, F .
ACTA CHEMICA SCANDINAVICA, 1998, 52 (08) :1024-1028
[9]
Eberson L., 1996, CHEM COMMUNICATIONS, V2105
[10]
Eberson L., 1995, J CHEM SOC P2, V2, P1735