Photolysis of chloride precursors as a method to prepare and characterize the triplet state of fluorenyl-substituted m-xylylene diradicals

被引:4
作者
Gajewski, JJ [1 ]
Paul, GC [1 ]
机构
[1] Indiana Univ, Dept Chem, Bloomington, IN 47405 USA
关键词
D O I
10.1016/S0040-4039(97)10598-6
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Fluorenyl substituted m-xylylene tripler diradicals are conveniently generated from the corresponding dichloride precursors upon pbotolysis at <100 K in 2-MeTHF glass. Under similar conditions tert-butyl substituted Schlenk type m-xylylene could not be generated from the dichloride precursor 6. Compound 6, however could be dehalogenated with zinc dust in both toluene and 2-MeTHF to produce the tripler diradical. (C) 1997 Elsevier Science Ltd. All rights reserved.
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页码:351 / 354
页数:4
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