4.5 Article

Halogenated Benzene Cation Radicals

期刊

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2013, 期 15, 页码 3131-3136

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201201691

关键词

Cations; Radical ions; Benzene cations; Jahn-Teller distortion

资金

  1. Deutsche Forschungsgemeinschaft (DFG) (Graduiertenkolleg, Fluorine as a Key Element)

向作者/读者索取更多资源

The benzene cation radicals [C6F5-CF3](+), [1,4-C6F4(CF3)(2)](+), [1,2,4,5-C6H2Cl4](+), [C6F5-C6F5](+), and [C6Br6](+) have been obtained as salts with fluoroarsenic and fluoroantimony counterions. Their structures have been obtained by single-crystal structure determinations, and supported by ESR measurements and DFT calculations. [C6F5-CF3](+), [1,4-C6F4(CF3)(2)](+), and [1,2,4,5-C6H2Cl4](+) have the predicted bisallyl type structure. [C6F5-C6F5](+) can be described as having a quinoid form with a strengthened central C-C bond and a smaller dihedral angle as compared to the neutral C6F5-C6F5. [C6Br6](+) is the missing link between [C6F6](+), [C6Cl6](+), and [C6I6](+). It has a Jahn-Teller distortion, though weaker than [C6F6](+) and [C6Cl6](+), in contrast to [C6I6](+), which remains in a regular hexagon structure.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据