On the relationship between the fullerene reactivity and degree of substitution


如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅存取

详细

The kinetics of radical polymerization of N-isopropylacrylamide (NIPA, initiator of AIBN) in the presence of some C60 derivatives was studied. It was established experimentally and by quantum chemical calculations that the ability of fullerene to add radicals decreased sharply after the destruction of six double bonds in the C60 molecule due to the addition of six free radicals or other particles. The calculations show that the energy of bond formation between the seventh initiator radical and C60 is by 20 times lower than that in the case of previous six radicals, and the further addition of radicals is impossible. It was experimentally found that the maximally possible number of added initiator radicals can be much higher. Moreover, during radical polymerization of NIPA a polymer layer grows around the C60 molecules with maximally possible number of already added initiator radicals. The layer consists of polymer NIPA chains chemically bound with C60. A possible mechanism explaining this fact is discussed.

作者简介

E. Atovmyan

Institute of Problems of Chemical Physics, Russian Academy of Sciences

编辑信件的主要联系方式.
Email: atovmyan@icp.ac.ru
俄罗斯联邦, 1 prosp. Akad. Semenova, Chernogolovka, Moscow Region, 142432

补充文件

附件文件
动作
1. JATS XML

版权所有 © Springer Science+Business Media, LLC, 2017