首页> 外文期刊>Radiation Physics and Chemistry >EPR STUDY OF CATION-RADICALS OF CYCLIC ALKENES IN CHLOROFLUOROCARBON MATRICES
【24h】

EPR STUDY OF CATION-RADICALS OF CYCLIC ALKENES IN CHLOROFLUOROCARBON MATRICES

机译:氯氟烃基中环烯烃的阳离子根基的EPR研究

获取原文
获取原文并翻译 | 示例
           

摘要

By gamma irradiation of cycloheptatriene, bicyclo(3.3.0)octene and dehydrodicyclopentadiene in chlorofluorocarbon matrices at 77 K the radical cations generated by electron loss from the parent molecules have been obtained and their electronic structure analyzed by EPR spectroscopy and by INDO and MNDO-PM3 molecular orbital calculations. On warming above 77 K these species undergo deprotonation to form neutral radicals. In the case of dicyclopentadiene the primary radical-cation is not stable at 77 K but decomposes probably by ring opening giving a bis-allylilic type cation-radical.
机译:通过在77 K的氯氟烃基质中对环庚三烯,双环(3.3.0)辛烯和脱氢二环戊二烯进行γ辐射,获得了由母体分子电子损失产生的自由基阳离子,并通过EPR光谱法,INDO和MNDO-PM3分析了它们的电子结构。分子轨道计算。在高于77 K的温度下,这些物质会发生去质子化反应,形成中性自由基。在二环戊二烯的情况下,伯自由基阳离子在77 K时不稳定,但可能通过开环分解而产生双烯丙基型阳离子自由基。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号