作者:Wafaa M Abdou、Yehia O Elkhoshnieh、Mahmoud M Sidky
DOI:10.1016/s0040-4020(01)87036-8
日期:1994.3
Photocleavage reactions of a wide range of ethylene compounds were investigated. Photosensitized oxygenation resulted in formation of their corresponding ketones. On the other hand, photoreaction of these substrates with elemental sulfur yielded the corresponding thioketones. Furthermore, photobehaviour of some ethylene episulfides also was studied. It could be concluded that UV-irradiation provides
研究了多种乙烯化合物的光解反应。光敏氧化导致形成它们相应的酮。另一方面,这些底物与元素硫的光反应产生了相应的硫代酮。此外,还研究了一些乙烯环硫化物的光行为。可以得出结论,紫外线辐射为此类化合物提供了快速有效的失活途径。