ABSTRACTInorganic-organic hybrid polymers were prepared by radical polymerization of
methacrylic acid or methyl methacrylate with the (meth) acrylate-substituted
oxozirconium and oxotitanium clusters
Zr6(OH)4O4(OMc)12(OMc =
methacrylate), Zr4O2(OMc)12,
Ti6O4(OEt)8(OMc)8 and
Ti4O2(OPri)6(OAcr)6(OAcr
= acrylate). A few mol% of cluster is sufficient for an efficient
cross-linking of the polymer chains. Small-angle X-ray scattering data
indicate that the cluster size is retained in the polymers and that the
microstructure of the cluster cross-linked samples can be described by a
dispersion of identical spherical or disk-shaped clusters in the polymer.
The obtained hybrid polymers exhibit a higher thermal stability because
depolymerization reactions are inhibited. Contrary to undoped poly (methyl
methacrylate), the cluster cross-linked polymers are insoluble but swell in
organic solvents. The solvent uptake upon swelling decreases with an
increasing amount of polymerized cluster.