Macromolecular Rapid Communications, Vol.22, No.15, 1272-1277, 2001
Synthesis of high-molar mass arborescent-branched polyglycidol via sequential grafting
Communication: A multiple grafting technique was used to synthesize arborescent-branched high-molecular mass poly(2,3-epoxypropan-1-ol). In the first step, linear polyglycidol ((M) over bar (n) = 10300) was obtained. Some of the hydroxyl groups were transformed into alcoholate anions in a reaction with potassium tert-butoxide, and the obtained polyanion was used to initiate the polymerization of 1-ethoxyethyl glycidyl ether, the glycidol having a protected hydroxyl group. Removing the protecting groups yielded polyglycidol-graft-polyglycidol. This procedure was repeated twice to give three generations of comb-burst branched polyglycidol chains with (M) over bar (n) of 8.2 x 10(4), 7.4 x 10(5) and 1.8 x 10(6).