Amounts between 2.5 and 5.9% of HBr, HCl and Cl-2 were added to fuller
ene forming benzene/oxygen/argon flat-flames burning at 75 mbar in an
attempt to affect halogen substitutions in the carbon framework. The i
nhibition effect of HBr dramatically reduced the yield of fullerene, w
hile it stayed in the same order of magnitude after addition of HCl or
Cl-2. No formation of halogenated fullerenic compounds could be detec
ted by mass spectrometry using chemical ionization with CH4/N2O or MAL
DI. The measurement of bromine- and chlorine-precursor mass spectra sh
owed the formation of a great number of bromine or chlorine containing
compounds, essentially polycyclic aromatic hydrocarbons (PAH). In the
case of HBr addition, only relatively small molecules could be observ
ed because reactions with bromine atoms are thermodynamically less fav
ourable in regions far from the burner with relatively high temperatur
es.