This work reports the use of benzophenone, a very
well characterized probe, to study new hosts (i.e., modified
celluloses grafted with alkyl chains bearing 12 carbon atoms)
by surface esterification. Laser-induced room temperature
luminescence of air-equilibrated or argon-purged solid
powdered samples of benzophenone adsorbed onto the two
modified celluloses, which will be named C12-1500 and
C12-1700, revealed the existence of a vibrationally structured
phosphorescence emission of benzophenone in the case where
ethanol was used for sample preparation, while a nonstructured
emission of benzophenone exists when water was used instead of
ethanol. The decay times of the benzophenone emission vary
greatly with the solvent used for sample preparation and do
not change with the alkylation degree in the range of
1500–1700 micromoles of alkyl chains per gram of cellulose.
When water was used as a solvent for sample preparation, the
shortest lifetime for the benzophenone emission was observed;
this result is similar to the case of benzophenone adsorbed
onto the “normal” microcrystalline cellulose
surface, with this latter case previously reported by Vieira
Ferreira et al. in 1995. This is due to the more efficient
hydrogen abstraction reaction from the glycoside rings of
cellulose when compared with hydrogen abstraction from the
alkyl chains of the modified celluloses. Triplet-triplet
transient absorption of benzophenone was obtained in both
cases and is the predominant absorption immediately after
laser pulse, while benzophenone ketyl radical formation occurs
in a microsecond time scale both for normal and modified
celluloses.