Novel plant‐oil‐derived long‐chain (C19 and C23) α,ω‐diisocyanates, optionally in combination with the corresponding long‐chain diols, provide entirely aliphatic hard segments in segmented thermoplastic polyurethane elastomers (TPUs), with carbohydrate‐based poly(trimethylene glycol) soft segments. Compared to materials based on a mid‐chain monomer analog, phase separation is higher due to an increased flexibility of the aliphatic segments. Although melting points are slightly lower than for HDPE, the long‐chain TPU's solid‐state structure is still dominated by hydrogen‐bonding.

In this study we describe the green synthesis of temperature-switchable polymer-magnetite nanoparticles (PMNPs) in water at room temperature via an improved co-precipitation pathway for reversible switchable superstructures.