影像科学与光化学 ›› 1996, Vol. 14 ›› Issue (4): 351-354.DOI: 10.7517/j.issn.1674-0475.1996.04.351

• 研究简报 • 上一篇    下一篇

光氧化反应研究 Ⅸ.N-叔丁基苯甲叉亚胺的光氧化反应

吴树屏1, 江致勤1, 贾发瑞2   

  1. 1. 同济大学化学系, 上海200092;
    2. 兰州大学应用有机化学国家重点实验室, 兰州730000
  • 收稿日期:1996-03-13 修回日期:1996-07-02 出版日期:1996-11-20 发布日期:1996-11-20
  • 通讯作者: 江致勤
  • 基金资助:
    国家自然科学基金

STUDIES ON PHOTOOXIDATION Ⅸ.PHOTOOXIDATION OF N-BENZYLIDINE-N-TERT-BUTYLIMINE

WU Shuping1, JIANG Zhiqin1, JIA Farei2   

  1. 1. Department of Chemistry, Tongji University, Shanghai 200092, P. R. China;
    2. National Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, P. R. China
  • Received:1996-03-13 Revised:1996-07-02 Online:1996-11-20 Published:1996-11-20

摘要: 对于含C=C和N=N双键化合物的光化学与光物理迄今已进行了广泛的研究,而介于其间的C=N双键类亚胺(imines)的光化学与光物理的探讨,由于视黄醛等涉及亚胺C=N键光化学的进展,而于近来得到重视.已知的C=N双键的光化学大多涉及环加成、重排、异构化和还原反应等[1],而亚胺的光氧化反应则报道较少.

关键词: 亚胺, 光氧化, 产物分布

Abstract: The self and sensitized photooxidation of imines,N-benzylidine-N-tert-butylimine(BBI) and N- phenyl-N-diphenylmethyleneimine(PDPMI), were investigated. It was found that BBI underwent a facile photooxidation. The reaction product distribution of BBI was determined, indicating oxidation-clevage mechanism may be involved. In contrast,PDPMI showed low reactivity to photooxidation.

Key words: imines, photooxidation, product distribution