BICYCLOPENTENE ADDEND ON [60]FULLERENE - EPOXIDATION AND CIS-BROMINE ADDITION

Citation
Mf. Meidine et al., BICYCLOPENTENE ADDEND ON [60]FULLERENE - EPOXIDATION AND CIS-BROMINE ADDITION, Perkin transactions. 2, (10), 1994, pp. 2125-2127
Citations number
10
Categorie Soggetti
Chemistry Physical","Chemistry Inorganic & Nuclear
Journal title
ISSN journal
03009580
Issue
10
Year of publication
1994
Pages
2125 - 2127
Database
ISI
SICI code
0300-9580(1994):10<2125:BAO[-E>2.0.ZU;2-9
Abstract
Bromine adds cis to the double bond in the addend of the [60]fullerene -cydopentadiene adduct, so that both bromines are directed away from t he cage. The epoxide,formed by peracetic acid oxidation of the double bond of the addend, also points away from the cage. These results are attributed to a combination of steric hindrance and polar repulsion by the fullerene cage, the first time such effects have been reported to control addition. The epoxide appears to extrude CO during mass spect rometry to give a cyclobutane derivative of [60]fullerene.