摘要
氮杂富勒烯是目前被重点关注的一类杂富勒烯,在化学合成方法中均需要经过开孔衍生物,然而对于氮杂富勒烯的前体开孔化合物—羰基内酰胺衍生物,人们的研究报道较少。本研究对其与富电子芳烃的亲电芳香取代反应进行了系统的研究。研究发现,反应除了生成单取代芳基氮杂[60]富勒烯,还有两个副产物。本论文对两个副产物进行了详细的表征和结构鉴定,这对后续开展氮杂富勒烯的深入研究提供了有利条件。
Azafullerene is one of the heterofullerenes which has been paid much attention.Open-cage fullerene derivatives are key intermediates to form aza[60]fullerene.However,the research of N-MEM-ketolactam derivative which is the precursor compound of azafullerene,is still quite rare.In this study,the electrophilic aromatic substitution reaction of N-MEM-ketolactam derivative with electron-rich aromatic hydrocarbons was extensively studied.The results indicate that the reaction afforded the monosubstituted aza[60]fullerene along with other two new by-products.Both of the by-products have been isolated and characterized.The research is very helpful in exploring their applications in materials science.
作者
周倩
朱琳
孙晃斌
陈思嫘
吴珮溪
许良
梁思思
Zhou Qian;Zhu Lin;Sun Huangbin;Chen Silei;Wu Peixi;Xu Liang;Liang Sisi(Department of Chemistry and Materials Science,Nanyue College of Hengyang Normal University,Hengyang 421008,China;College of Chemistry and Materials Science,Hengyang Normal University,Hengyang 421008,China)
出处
《山东化工》
CAS
2019年第9期50-51,共2页
Shandong Chemical Industry
基金
湖南省大学生研究性学习和创新实验计划(No.NYD201808
NYD201702)
衡阳师范学院科学基金(No.16D05
17D08)
国家自然科学基金项目(No.21602210)
关键词
氮杂单取代富勒烯
化学合成
条件优化
机理
N-MEM-ketolactam derivative
electrophilic aromatic substitution
Azafullerene
mechanism