This work focused on surface modification of magnetite nanoparticle (MNP) with poly(poly(ethylene glycol) monomethyl ether methacylate)-b-(poly(N-isopropylacrylamide)-st-poly(thiolactone acrylamide)), PPEGMA-b-(PNIPAAm-st-PTlaAm), diblock copolymer, synthesized via reversible addition-fragmentation chain transfer (RAFT) polymerization to obtain the particles having good water dispersible PPEGMA brushes, thermo-responsive PNIPAAm, and reactive thiolactone groups of PTlaAm.The thiolactone moiety in the copolymer can readily react with amino groups grafted on MNP surface and essentially induced the formation of MNP nanocluster.According to transmission electron microscopy (TEM), the size of the nanocluster ranged between 200 and 500 nm per cluster with 8 to 10 nm in diameter for each particle. Hydrodynamic diameter of the nanocluster significantly decreased as the dispersion temperature increased from 25 C to 45 C due to the shrinkage of thermo-responsive PNIPAAm when crossing its lower critical solution temperature (LCST). This stable nanocluster might be potentially used as a magnetic carrier for control release of entrapped entities with a thermally triggering mechanism. K E Y W O R D S magnetite, nanocluster, thermo-responsive, thiolactone, water dispersible
A thermoresponsive and recyclable nanomaterial was synthesized by surface modification of magnetite nanoparticles (MNPs) with poly(N-isopropylacrylamide-co-diethylaminoethyl methacrylate) (P(NIPAAm-co-DEAEMA)), having PNIPAAm as a thermoresponsive moiety and PDEAEMA for catalyst binding. Palladium (Pd) nanoparticles were incorporated into this material, and the resulting nanocatalyst was efficient in the hydrogenation of olefins and nitro compounds with turnover frequencies (TOFs) up to 750 h −1 . Consistent catalytic activity in 10 consecutive runs was observed when performing the hydrogenation at 45 °C, i.e., above the lower critical solution temperature (LCST) of the copolymer (37 °C), followed by cooling to 15 °C, i.e., below the LCST of the copolymer.
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