全氟烷基化菲-9,10-邻醌制全氟烷基化二苯酐的清洁光化学转化

IF 1.9 4区 化学 Q3 CHEMISTRY, INORGANIC & NUCLEAR
Shankar Gairhe, Mason Ferrie, Haoran Sun
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引用次数: 0

摘要

在光照射下,羰基化合物与激发态猝灭剂分子氧相互作用,通过能量转移形成三重态氧加合物或单线态氧。对于菲-9,10-o-醌,分子氧通常加入到分子结构中形成三重态氧加合物,然后转化为不同的最终产物,通常是复杂的混合物。在这里,我们报道了全氟烷基化菲-9,10-o-醌只经过光介导转化为二苯酸酐衍生物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Clean photochemical conversion of perfluoroalkylated phenanthrene-9,10-o-quinones to perfluoroalkylated diphenic anhydrides

Clean photochemical conversion of perfluoroalkylated phenanthrene-9,10-o-quinones to perfluoroalkylated diphenic anhydrides
Under light irradiation, carbonyl compounds interact with molecular oxygen, a common excited state quencher, resulting in the formation of either triplet state-oxygen adducts or singlet oxygen via energy transfer. With phenanthrene-9,10-o-quinones, molecular oxygen usually adds on molecular structures forming triplet state-oxygen adducts which then convert to different final products, often complex mixtures. Here, we report that perfluoroalkylated phenanthrene-9,10-o-quinones exclusively undergo light mediated transformation into diphenic anhydride derivatives.
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来源期刊
Journal of Fluorine Chemistry
Journal of Fluorine Chemistry 化学-无机化学与核化学
CiteScore
3.80
自引率
10.50%
发文量
99
审稿时长
33 days
期刊介绍: The Journal of Fluorine Chemistry contains reviews, original papers and short communications. The journal covers all aspects of pure and applied research on the chemistry as well as on the applications of fluorine, and of compounds or materials where fluorine exercises significant effects. This can include all chemistry research areas (inorganic, organic, organometallic, macromolecular and physical chemistry) but also includes papers on biological/biochemical related aspects of Fluorine chemistry as well as medicinal, agrochemical and pharmacological research. The Journal of Fluorine Chemistry also publishes environmental and industrial papers dealing with aspects of Fluorine chemistry on energy and material sciences. Preparative and physico-chemical investigations as well as theoretical, structural and mechanistic aspects are covered. The Journal, however, does not accept work of purely routine nature. For reviews and special issues on particular topics of fluorine chemistry or from selected symposia, please contact the Regional Editors for further details.
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