期刊文献+

Overwhelming decomposition of 4-bromo-4'-cyanomethylbiphenylyl radical anion without electron transfer to 4,4'-dibromobiphenyl

Overwhelming decomposition of 4-bromo-4'-cyanomethylbiphenylyl radical anion without electron transfer to 4,4'-dibromobiphenyl
原文传递
导出
摘要 Dibromobiphenyl reacted with cynomethyl anion in ammonia under irradiation to form nucleophilic bis-substituted product in high yield without substantial monosubstituted product. Quantum yields for the formations of bis- and monosubstituted products were found to be 85.6 and 2.3×10-6 respectively, while the corresponding pseudo-first-order rates were 6.9×10-3 and 5.2×10-10 mol.L-1.S-1. Block up the possible electron transfer of 4-brome-4'-cyanomethylbiphenylyl radical anion to 4-cyanometbyl-biphenylyl radical and bromine ion. Dibromobiphenyl reacted with cynomethyl anion in ammonia under irradiation to form nucleophilic bis-substituted product in high yield without substantial monosubstituted product. Quantum yields for the formations of bis- and monosubstituted products were found to be 85.6 and 2.3×10-6 respectively, while the corresponding pseudo-first-order rates were 6.9×10-3 and 5.2×10-10 mol.L-1.S-1. Block up the possible electron transfer of 4-brome-4'-cyanomethylbiphenylyl radical anion to 4-cyanometbyl-biphenylyl radical and bromine ion.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 1994年第2期148-157,共10页 中国化学(英文版)
基金 Project supported by the National Natural Science Foundation of China.
关键词 PHOTOCHEMISTRY SRN1 reaction electron transfer dibromobiphenyl. Photochemistry, SRN1 reaction, electron transfer, dibromobiphenyl.
  • 相关文献

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部