[60]- and [70]Fullerenes are trifluoromethylated across 5:6-bonds
Тип публикации: Journal Article
Дата публикации: 2003-05-30
scimago Q1
wos Q2
БС1
SJR: 1.037
CiteScore: 7.4
Impact factor: 4.2
ISSN: 13597345, 1364548X
PubMed ID:
12841248
Materials Chemistry
Metals and Alloys
Surfaces, Coatings and Films
General Chemistry
Ceramics and Composites
Electronic, Optical and Magnetic Materials
Catalysis
Краткое описание
Trifluoromethylation of [60]- and [70]fullerenes occurs across both 6:6- and 5:6-bonds giving unsymmetrical tetramethyl adducts having four contiguous CF3 groups; both fullerenes give bis adducts which do not involve 6:6-addition, and unsymmetrical hexa-adducts (with contiguous CF3 groups) are also obtained from [60]fullerene.
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ГОСТ
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Darwish A. D. et al. [60]- and [70]Fullerenes are trifluoromethylated across 5:6-bonds // Chemical Communications. 2003. Vol. 12. p. 1374.
ГОСТ со всеми авторами (до 50)
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Darwish A. D., Avent A. G., Abdul-Sada A. K., Taylor R. [60]- and [70]Fullerenes are trifluoromethylated across 5:6-bonds // Chemical Communications. 2003. Vol. 12. p. 1374.
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TY - JOUR
DO - 10.1039/b303496h
UR - https://doi.org/10.1039/b303496h
TI - [60]- and [70]Fullerenes are trifluoromethylated across 5:6-bonds
T2 - Chemical Communications
AU - Darwish, Adam D
AU - Avent, Anthony G.
AU - Abdul-Sada, Ala’a K.
AU - Taylor, Roger
PY - 2003
DA - 2003/05/30
PB - Royal Society of Chemistry (RSC)
SP - 1374
IS - 12
PMID - 12841248
SN - 1359-7345
SN - 1364-548X
ER -
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BibTex (до 50 авторов)
Скопировать
@article{2003_Darwish,
author = {Adam D Darwish and Anthony G. Avent and Ala’a K. Abdul-Sada and Roger Taylor},
title = {[60]- and [70]Fullerenes are trifluoromethylated across 5:6-bonds},
journal = {Chemical Communications},
year = {2003},
publisher = {Royal Society of Chemistry (RSC)},
month = {may},
url = {https://doi.org/10.1039/b303496h},
number = {12},
pages = {1374},
doi = {10.1039/b303496h}
}