Redox and EPR spectral behaviour of radical cations of dibenzothiophene and some of its derivatives

被引:10
|
作者
Eberson, L [1 ]
Hartshorn, MP [1 ]
Persson, O [1 ]
Radner, F [1 ]
机构
[1] UNIV CANTERBURY,DEPT CHEM,CHRISTCHURCH 1,NEW ZEALAND
来源
ACTA CHEMICA SCANDINAVICA | 1997年 / 51卷 / 04期
关键词
D O I
10.3891/acta.chem.scand.51-0492
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The radical cations of dibenzothiophene 1 and its 2,8-[H-2(2)]-isotopomer (2), a series of methylated dibenzothiophenes, viz. 2,8- (3), 3,7- (4) and 4,6-dimethyldibenzothiophene (5), and 2,4,6,8-tetramethyldibenzothiophene (6), as well as 2,2'-(7) and 4,4'-bidibenzothiophene (8) have been generated in 1,1,1,3,3,3-hexafluoropropan-2-ol, mostly by Tl-III trifluoroacetate or 4-tolyl-Tl-III trifluoroacetate oxidation. From the hyperfine coupling constants obtained, it is concluded that the 2- and 4-positions of 1(.+) are the carbon atoms possessing the highest spin density. This assignment agrees with results of high-level quantum-chemical calculations, placing the B-2(1) state as the lowest energy level of 1(.+).
引用
收藏
页码:492 / 500
页数:9
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