ORIGINAL CONTRIBUTION Evolution of high-temperature molecular relaxations in poly(2-(2-methoxyethoxy)ethyl methacrylate)

rylate (poly(MEO2MA)) are regarded as bioinert replace-ments of poly(N-isopropylacrylamide) in some biomedical applications. Networks of poly(MEO2MA) of various archi-tecture form thermo-responsive hydrogels. Here, we present dielectric and mechanical spectroscopy studies on segmental motions and network relaxation processes in linear poly(MEO2MA) and its networks — bare network and the network grafted with short poly(MEO2MA) chains. We show that the α process assigned to the segmental motions of poly(MEO2MA) is independent on the polymer topology and the glass transition temperature, Tg, associated with this process equals 235–236 K for all investigated systems. The α′ relaxation observed above Tg by dynamical mechanical anal-ysis is assigned to the sub-Rouse process. It strongly depends on the polymer network architecture and slows down by four orders of magnitude upon network formation