Ly. Chiang et al., EVIDENCE OF HEMIKETALS INCORPORATED IN THE STRUCTURE OF FULLEROLS DERIVED FROM AQUEOUS ACID CHEMISTRY, Journal of the American Chemical Society, 115(13), 1993, pp. 5453-5457
We have characterized and elucidated the chemical structure of fullero
ls, prepared from the aqueous acid reaction of C60 in the presence of
sulfuric acid and nitric acid, consisting of hemiketal moieties in add
ition to tertiary hydroxy groups, In the aqueous reaction, a high yiel
d of fullerols was obtained utilizing potassium nitrate as an effectiv
e precursor for generating nitric acid in situ. Evidence for the hemik
etal structure is given by an observation of chemical shifts of vinyl
ether carbons and ketal carbons centered at delta 170.3 and 100.0, res
pectively, in the C-13 NMR spectrum of fullerols. This structure was a
lso substantiated by several spectroscopic methods including XPS, TGA-
MS, and TGA-FTIR. Interestingly, the reversible interconversion reacti
on of hemiketal moieties in fullerol to the corresponding ketone upon
variation of pH in aqueous solution provided conclusive results to ver
ify the presence of hemiketal functions. This is the first observation
of hemiketal functions incorporated onto the fullerene cage structure
.