Room temperature solution studies of complexation between o-chloranil and a series of anilines by spectrophotometric method

被引:35
作者
Bhattacharya, S [1 ]
Banerjee, M [1 ]
Mukherjee, AK [1 ]
机构
[1] Univ Burdwan Golapbag, Dept Chem, Burdwan 713104, W Bengal, India
关键词
o-chloranil; EDA complex; electron affinity; formation constant; kinetic study;
D O I
10.1016/S1386-1425(01)00427-9
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Electron donor-acceptor (EDA) complex formation between o-chloranil and a series of anilines has been studied in CCl4 medium. In all the cases, EDA complexes are formed instantaneously on mixing the donor and acceptor solutions. N,N-dimethylaniline and NN-dimethyl-p-toluidine form stable EDA complexes with o-chloranil while the other complexes decay slowly into secondary products. The kinetics of all these reactions has been studied by UV-VIS absorption spectrophotometric method and the rate constants of the reactions and formation constants of the EDA complexes have been determined. The charge transfer (CT) transition energies of the complexes are found to change systematically with change in the number and position of the methyl groups in the donor molecules (methylanilines). From an analysis of this variation, the electron affinity of o-chloranil has been found to be 2.54 eV. A perturbational inductive effect Huckel parameter h(Me) has been found from this trend and the value obtained (-0.27) is very close to that (-0.3) obtained by Lepley (J. Am. Chem. Soc., 86 (1964) 2545) from a study of tetracyano ethylene (TCNE)-methylbenzene complexes. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:2409 / 2416
页数:8
相关论文
共 32 条
[1]   Structural changes in W/O Triton X-100/cyclohexane-hexanol/water microemulsions probed by a fluorescent drug Piroxicam [J].
Andrade, SM ;
Costa, SMB ;
Pansu, R .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2000, 226 (02) :260-268
[2]  
[Anonymous], 1964, ANGEW CHEM-GER EDIT
[3]   A SPECTROPHOTOMETRIC INVESTIGATION OF THE INTERACTION OF IODINE WITH AROMATIC HYDROCARBONS [J].
BENESI, HA ;
HILDEBRAND, JH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1949, 71 (08) :2703-2707
[4]  
BRIEGLEB G, 1959, Z ELEKTROCHEM, V63, P6
[5]  
BRUEGGERMANN K, 1992, J PHYS CHEM-US, V96, P4405
[6]   Charge-transfer complex formation between o-chloranil and a series of polynuclear aromatic hydrocarbons [J].
Chakraborty, B ;
Mukherjee, AK ;
Seal, BK .
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 2001, 57 (02) :223-229
[7]  
Chakravarty B, 1998, INDIAN J CHEM A, V37, P865
[8]   Photophysics of 1-dimethylaminonaphthalene in aqueous-organic binary solvents [J].
Chen, H ;
Jiang, YB .
CHEMICAL PHYSICS LETTERS, 2000, 325 (5-6) :605-609
[9]   THE ELECTRONIC STRUCTURE OF CONJUGATED SYSTEMS .1. GENERAL THEORY [J].
COULSON, CA ;
LONGUETHIGGINS, HC .
PROCEEDINGS OF THE ROYAL SOCIETY OF LONDON SERIES A-MATHEMATICAL AND PHYSICAL SCIENCES, 1947, 191 (1024) :39-60
[10]   Surface catalyzed electron transfer from polycyclic aromatic hydrocarbons (PAH) to methyl viologen dication: evidence for ground-state charge transfer complex formation on silica gel [J].
Dabestani, R ;
Reszka, KJ ;
Sigman, ME .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 1998, 117 (03) :223-233