Gm. Stewart et Ma. Fox, CHROMOPHORE-LABELED DENDRONS AS LIGHT-HARVESTING ANTENNAE, Journal of the American Chemical Society, 118(18), 1996, pp. 4354-4360
A novel series of polyether dendrimer segments (dendrons) end-clipped
with pyrenyl, naphthyl, or methyl groups has been prepared by a conver
gent growth method. Steady-state fluorescence measurements indicate th
e absence of intramolecular naphthalene excimer in the naphthyl-capped
dendrons. However, in the pyrenyl-capped dendrons, excimer emission p
redominates. Fluorescence from both the naphthyl monomer and pyrenyl e
xcimer are quenched when a suitable electron donor (e.g., a 3-[dimethy
lamino]phenoxy group) is covalently attached at the dendron focal poin
t. No sensitized emission from the dendron backbone is observed in the
chromophore-labeled dendrons, although the control methyl-capped dend
ron fluoresces weakly at 310 nn when excited at 284 nm. Absorption and
fluorescence spectra, fluorescence quantum yields, and fluorescence l
ifetimes for the chromophore-labeled dendrons are reported.