Cyclohexane in nanotubes: Direct chair–chair interconversion
- Авторлар: Kuznetsov V.1,2
-
Мекемелер:
- Ufa State Aviation Technical University
- Ufa State Petroleum Technological University
- Шығарылым: Том 87, № 11 (2017)
- Беттер: 2558-2562
- Бөлім: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/221560
- DOI: https://doi.org/10.1134/S1070363217110081
- ID: 221560
Дәйексөз келтіру
Аннотация
DFT PBE/3ζ study of conformational transformations of cyclohexane inside nanotubes with chirality indices of (8,0) and (5,5) showed that the encapsulated molecule is characterized by shortened C–C bonds, some electric charge, and reduced barrier to chair–chair interconversion in comparison to the free molecule. Unlike free cyclohexane, no twist conformer as intermediate minimum on the potential energy surface was localized for the encapsulated molecule.
Негізгі сөздер
Авторлар туралы
V. Kuznetsov
Ufa State Aviation Technical University; Ufa State Petroleum Technological University
Хат алмасуға жауапты Автор.
Email: kuzmaggy@mail.ru
Ресей, ul. K. Marksa 12, Ufa, 450008; ul. Kosmonavtov 1, Ufa, 450062