The presence of fullerenes up to C-116 was observed in condensable mat
erial from a benzene/oxygen flame. The flame material was Soxhlet-extr
acted with toluene for 363 h, fractionationed by means of a silica-bas
ed semipreparative HPLC column, and analyzed by HPLC coupled to a mass
spectrometer via a heated nebulizer interface using a 2-(1-pyrenyl)et
hylsilica stationary phase. UV-vis spectra were measured for C-60, C60
O, C-60. CH4, C-70, C70O, C-76, C-78, C-80, C-84, a C-84 adduct, C-86,
C-88, C-90, C-92, C-94, C-96, C-98, C-1OO, C-102, and C-108. Isomers
could be discerned for C-78, C-90, and C-94. A calibration using exter
nal standards was performed for C-60, C-70, C-76, C-78, and C-84. For
all other species the relative abundances were estimated based on HPLC
peak integration results. Electric are soot was extracted under simil
ar conditions and the quantification of fullerenes compared to the dat
a obtained with flame-generated condensable material. Except for C-60
and C-76, the abundances were significantly higher in the case of flam
e-generated condensable material. Also, striking differences between t
he two fullerene production methods are seen in the relative abundance
s of C-78 isomers. Considering the present results and the ease with w
hich the experimental setup could be scaled up, flame-generated conden
sable material represents an excellent starting material for the prepa
rative isolation of higher fullerenes.