New siloxane coupling agents have been prepared by the platinum-cataly
zed addition of C-H2=CHSi(OR)(3) silanes (R = CH3 or CH2CH2OCH3) to fo
ur different siloxanes, oly[(methylhydrogen)siloxane-co-dimethylsiloxa
ne], poly[(methylhydrogen)siloxane] (dp = 33), tetramethyldisiloxane,
and tetramethylcyclotetrasiloxane. These new hydrophobic materials off
er a distinct alternative to conventional silane coupling agents, prev
alent in many industrial applications. The new preparations allow for
control of molecular weight, the extent of coupling functionality, and
the distribution of coupling groups on the siloxane backbone. The use
of 2D NMR experiments, COSY, and HETCOR indicated two modes of additi
on to the Si-H groups had occurred, Markovnikov and anti-Markovnikov.
GPC, FTIR, and H-1 and C-13 NMR were used to thoroughly characterize a
ll the reaction products.