Isolation and characterization of unsymmetrical C60Me5O3H, a cage-opened bisepoxide ketone: Tautomerism involving a fullerene cage bond

Citation
H. Al-matar et al., Isolation and characterization of unsymmetrical C60Me5O3H, a cage-opened bisepoxide ketone: Tautomerism involving a fullerene cage bond, ORG LETT, 3(11), 2001, pp. 1669-1671
Citations number
8
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
ORGANIC LETTERS
ISSN journal
15237060 → ACNP
Volume
3
Issue
11
Year of publication
2001
Pages
1669 - 1671
Database
ISI
SICI code
1523-7060(20010531)3:11<1669:IACOUC>2.0.ZU;2-V
Abstract
[GRAPHICS] Bisepoxide ketone C60Me5O3H, possessing a nine-membered hole in the cage, h as been isolated from the reaction of C60Cl6 with methyllithium followed by hydrolysis, It is a tautomer of the recently isolated bisepoxide fullereno l, this tautomerism being the first example. involving a cage C-C bond, and may be driven by cage strain. Like the fullerenol, the ketone gives a high C-58(+) fragmentation ion intensity during El mass spectrometry.