C60O3, a fullerene ozonide: Synthesis end dissociation to C60O and O-2

Citation
D. Heymann et al., C60O3, a fullerene ozonide: Synthesis end dissociation to C60O and O-2, J AM CHEM S, 122(46), 2000, pp. 11473-11479
Citations number
28
Categorie Soggetti
Chemistry & Analysis",Chemistry
Journal title
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
ISSN journal
00027863 → ACNP
Volume
122
Issue
46
Year of publication
2000
Pages
11473 - 11479
Database
ISI
SICI code
0002-7863(20001122)122:46<11473:CAFOSE>2.0.ZU;2-T
Abstract
An unstable intermediate has been detected and isolated in the reaction of ozone with C-60 in solution. On the basis of its UV-vis absorption spectrum , the measured release of O-2 in its decay to the epoxide C60O, and the fir st-order kinetics of this reaction, the intermediate has been identified as C60O3, a primary ozonide. This [6,6]-closed adduct of ozone with C-60 ther mally dissociates to C60O plus O-2 in toluene solution, octane solution, an d the solid phase with rate constants (at 23 degreesC) of 4.6 x 10(-2), 1.3 x 10(-3): and 3.0 x 10(-3) min(-1), respectively. The activation energy fo r dissociation in toluene solution is approximately 89 kJ mol(-1) Semiempir ical quantum calculations indicate that the formation and subsequent dissoc iation of C60O3 are both exothermic processes. These findings constitute th e first observation of a fullerene ozonide.