Modeling the morphology and mechanical behavior of shape memory polyurethanes based on solid-state NMR and synchrotron SAXS/WAXDThis paper is part of a Journal of Materials Chemistry themed issue on Actively Moving Polymers. Guest editor: Andreas Lendlein

A combination of solid-state proton Wide-line Nuclear Magnetic Resonance (NMR) relaxometry and synchrotron Small-angle (SAXS) and Wide-angle (WAXD) X-ray scattering was used to elucidate the microphase morphology of shape memory thermoplastic multi-block polyurethanes based on poly( -caprolactone), as switching segment and polyurethane based permanent or hard segments (HS). The polyurethanes are produced from the condensation of 1,4-butanediol (BDO) with hexamethylenediisocyanate (HDI). The morphology - induced by the hard-segment crystallization - converts from dispersed randomly placed hard-segment domains into progressively more periodic, but interconnected HS nanophases with increasing HS content. Irrespective of the actual morphology, the SAXS data could be described satisfactorily by using a clipped Gaussian random field (GRF) model. The NMR data demonstrate that the HS domain fraction corresponds to the chemical feed, pointing at a complete phase separation. The material mechanical behavior during repeated deformation cycles can be explained on morphological grounds and involves a spatially heterogeneous plastic deformation of the hard domains. The microphase morphology of shape memory thermoplastic multi-block polyurethanes and its response to mechanical loading were elucidated by a combination of solid-state NMR and synchrotron SAXS/WAXD.