New methods for the accurate determination of extinction and diffusion coefficients of aromatic and heteroaromatic radical anions in N,N-dimethylformamide

被引:76
作者
Pedersen, SU [1 ]
Christensen, TB [1 ]
Thomasen, T [1 ]
Daasbjerg, K [1 ]
机构
[1] Aarhus Univ, Dept Chem, DK-8000 Aarhus, Denmark
来源
JOURNAL OF ELECTROANALYTICAL CHEMISTRY | 1998年 / 454卷 / 1-2期
关键词
extinction coefficients; diffusion coefficients; aromatic; heteroaromatic; radical anions;
D O I
10.1016/S0022-0728(98)00195-8
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Two electrochemical methods are presented that allow an easy access to highly accurate UV-visible spectra of aromatic and heteroaromatic radical anions with life times longer than 50 s in N,N-dimethylformamide. The uncertainty on the extinction coefficients obtained is estimated to be as low as 5% which is a significant improvement in accuracy compared with other methods. The study has involved the radical anions of benzophenone, fluorenone, 1,4-naphthoquinone, anthraquinone, 1,2-benzanthraquinone, (E)-stilbene, anthracene, 9,10-diphenylanthracene, fluoranthene, perylene, benzonitrile, p-tolunitrile, 1,4-diacetylbenzene, 1,4-dicyanobenzene, 9,10-dicyanoanthracene, (E)-azobenzene, (E)-4-methoxycarbonylazobenzene, quinoxaline and phenazine. The first method takes advantage of a galvanostatic generation of the radical anions from the parent compounds combined with the recording of the absorbance at specific wavelengths by means of a so-called dip probe. The second technique described is based on the continuous and complete electroreduction of the aromatic compounds in an efficient electrochemical flow cell placed just ahead of a quartz cuvette in a traditional diode-array spectrometer. The successful strategy of combining a galvanostatic generation of aromatic radical anions with the measurement of a characteristic physical property has also been employed in the determination of diffusion coefficients. The recording device is here a rotating disc electrode. (C) 1998 Elsevier Science S.A. All rights reserved.
引用
收藏
页码:123 / 143
页数:21
相关论文
共 57 条
[1]  
Albery W.J., 1971, Ring-disc electrodes
[2]   ELECTRONIC-STRUCTURE AND NEAR-INFRARED SPECTRA OF DIQUINONE ANION RADICALS [J].
ALMLOF, JE ;
FEYEREISEN, MW ;
JOZEFIAK, TH ;
MILLER, LL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (03) :1206-1214
[3]   ABSOLUTE DETERMINATION OF ELECTRON CONSUMPTION IN TRANSIENT OR STEADY-STATE ELECTROCHEMICAL TECHNIQUES [J].
AMATORE, C ;
AZZABI, M ;
CALAS, P ;
JUTAND, A ;
LEFROU, C ;
ROLLIN, Y .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1990, 288 (1-2) :45-63
[4]  
ANGEL SM, 1991, CHEM SENS TECHNOL, V3, P163
[5]   METAL HYDRIDE REDUCTIONS VIA SINGLE ELECTRON-TRANSFER .2. EVIDENCE FOR AN ELECTRON-TRANSFER PATHWAY IN THE REACTIONS OF SIMPLE AND COMPLEX METAL-HYDRIDES OF THE MAIN GROUP-METALS WITH POLYNUCLEAR HYDROCARBONS [J].
ASHBY, EC ;
GOEL, AB ;
DEPRIEST, RN ;
PRASAD, HS .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1981, 103 (04) :973-975
[6]   USE OF MICROELECTRODES FOR THE RAPID-DETERMINATION OF THE NUMBER OF ELECTRONS INVOLVED IN AN ELECTRODE-REACTION [J].
BARANSKI, AS ;
FAWCETT, WR ;
GILBERT, CM .
ANALYTICAL CHEMISTRY, 1985, 57 (01) :166-170
[7]   SCANNING ELECTROCHEMICAL MICROSCOPY - THEORY AND APPLICATION OF THE TRANSIENT (CHRONOAMPEROMETRIC) SECM RESPONSE [J].
BARD, AJ ;
DENAULT, G ;
FRIESNER, RA ;
DORNBLASER, BC ;
TUCKERMAN, LS .
ANALYTICAL CHEMISTRY, 1991, 63 (13) :1282-1288
[8]  
BARD AJ, 1980, ELECTROCHEMICAL METH
[9]  
BIONDI C, 1981, J ELECTROANAL CHEM, V117, P201
[10]   EXCITED-STATE BEHAVIOR OF THERMALLY STABLE RADICAL IONS [J].
BRESLIN, DT ;
FOX, MA .
JOURNAL OF PHYSICAL CHEMISTRY, 1994, 98 (02) :408-411