A series of highly compact globular dendrimers, 5, 21, and 22, involving a
C-60 core with a T-h symmetrical addition pattern was synthesized by way of
the fivefold cyclopropanation of the fullerene-porphyrin dyad 2 with dendr
itic malonates in the remaining octahedral positions. Whereas 5 contains cl
assical Frechet benzyl-ether-based systems, a new type of dendra containing
a flexible spacer between the branching units was developed for the synthe
sis of 21 and 22. The spectroscopic, electrochemical, and photophysical pro
perties of the tetraphenylporphyrin-zinc (Zn-TPP) chromophore within the fu
nctional dendrimers depend not only on the presence but also on the generat
ion number of the surrounding dendra and therefore on the nanoenvironment p
rovided by the neighboring addends. This is reflected, for example, in the
bathochromic shifts of the Soret and Q-bands of the porphyrin moiety and in
the shift of the first reduction potentials to more negative values for bo
th the fullerene and porphyrin moieties with increasing generation number.
Whereas in the dyad 2 a photsinduced electron transfer from the porphyrin t
o the fullerene can occur, dendrimers 21 and 22 show fluorescence propertie
s and singlet oxygen formation properties (Phi(Delta) = 0.66-0.67) reminisc
ent to those of the parent Zn-TPP.