Degradable dendrimers are prepared as a template to create utrasmall c
ells when they get embedded in a polymer resin and to obtain well-defi
ned cavities with particular chemical groups at their walls if the end
groups remain attached to the matrix. In a first approach cascade: (13
-oxa-1-methylsilaundecenylidene): undecene was synthesised by the poly
addition reaction of methyl-di-undecenoxysilane as basic repeat unit.
A multimodal weight distribution was found which appeared to be selfco
ntrolled to a limited molecular weight. Degradation was done with dry
methanol and methanol with aqueous hydrochloric acid. In the case of d
ry methanol the degradation products yielded only low molecular weight
compounds while siloxane bonds were formed in the case the degradatio
n was performed with methanol and aqueous hydrochloric acid. In order
to create films with nanocavities, the degradable dendritic macromolec
ules were embedded in a methacrylate resin. Hole formation was illustr
ated by transmission electron microscopy for the case of 0.5 wt.-%, 5
wt.-% and 30 wt.-% of dendrimer content, However, aggregation of the d
endritic molecules during the curing of the methacrylate resin could n
ot be avoided. In order to sup press aggregation, cascade: (1-methylsi
lapropylidene): propene with methacrylate endgroups have been prepared
which can be covalently linked to the embedding resin molecules. In a
first approach the compatibility with the methacrylate resin was indi
cated by the optical transparency, while microscopy techniques were no
t capable to resolve the fine structure.