Trifunctional incompletely
condensed polyhedral oligomeric silsesquioxanes
(RSiMe
2
O)
3
R′
7
Si
7
O
9
(
IC-POSS
s) are considered as intriguing
building nanoblocks dedicated to constructing highly advanced organic–inorganic
molecules and polymers. Up to now, they have been mainly obtained
via
hydrosilylation of olefins, while the hydrosilylation
of the C≡C bonds has not been studied at all, despite the enormous
potential of this approach resulting from the possibility of introducing
3, 6, or even more functional groups into the
IC-POSS
structure. Therefore, in this work, we present a highly selective
and efficient synthesis of the first example of tripodal alkenyl-functionalized
IC-POSS
s, obtained
via
platinum-catalyzed
hydrosilylation of the terminal and internal alkynes, as well as symmetrically
and nonsymmetrically 1,4-disubstituted buta-1,3-diynes with silsesquioxanes
(HSiMe
2
O)
3
R′
7
Si
7
O
9
(R′ =
i
-C
4
H
9
(
1a
), (H
3
C)
3
CH
2
C(H
3
C)HCH
2
C (
1b
)). The resulting
products are synthetic intermediates that contain C=C bonds
and functional groups (e.g., OSiMe
3
, SiR
3
, Br,
F, B(O(C(CH
3
)
2
)
2
(Bpin)), thienyl),
which make them suitable for application in the synthesis of novel,
complex, hybrid materials with unique properties.