The polymerisation of oligo(ethylene glycol methyl ether) methacrylate from a multifunctional poly(ethylene imine) derived amide: a stabiliser for the synthesis and dispersion of magnetite nanoparticlesElectronic supplementary information (ESI) available: Plots of Cu(ii) function with time; UV-vis absorption spectra of Cu(i)Cl, Cu(ii)Cl2 and Cu(ii)Br2 solutions with DiMePiVA; X-ray diffraction pattern of PEI-graft-POEGMA stabilised nanoparticles; high magnification TEM images of magnetite nanopa

A facile synthetic route to poly(ethylene imine)- graft -poly(oligo(ethylene glycol methyl ether)) (PEI- graft -POEGMA) functionalised superparamagnetic magnetite nanoparticles is described. The polymerisation of OEGMA from a model molecular amide demonstrated the feasibility of POEGMA synthesis und...

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Hauptverfasser: Kleine, Aaron, Altan, Cem L, Yarar, U. Ecem, Sommerdijk, Nico A. J. M, Bucak, Seyda, Holder, Simon J
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Bucak, Seyda
Holder, Simon J
description A facile synthetic route to poly(ethylene imine)- graft -poly(oligo(ethylene glycol methyl ether)) (PEI- graft -POEGMA) functionalised superparamagnetic magnetite nanoparticles is described. The polymerisation of OEGMA from a model molecular amide demonstrated the feasibility of POEGMA synthesis under mild ATRP conditions (20 °C in ethanol) albeit with low initiator efficiencies. DFT studies suggest that the amide functionality is intrinsically of lower activity than ester functional monomers and initiators for atom transfer polymerisation (ATRP) as a consequence of higher bond dissociation energies and bond dissociation free energies (BDFE). However these studies further highlighted that use of an appropriate solvent could reduce the free energy of dissociation thereby reducing the relative difference in BDFE between the ester and amide groups. A commercial branched PEI sample was functionalised by reaction with 2-bromo-2-methylpropanoyl bromide giving an amide macroinitiator suitable for the atom transfer radical polymerisation (ATRP) of oligo(ethylene glycol methyl ether) methacrylate. The resulting PEI- graft -POEGMA copolymers were characterised by SEC, FT-IR and 1 H and 13 C NMR spectroscopy. PEI- graft -POEGMA coated magnetite nanoparticles were synthesised by a basic aqueous co-precipitation method and were characterised by transmission electron microscopy, thermogravimetric analysis and vibrating sample magnetometry and dynamic light scattering. These copolymer coated magnetite nanoparticles were demonstrated to be effectively stabilised in an aqueous medium. Overall the particle sizes and magnetic and physical properties of the coated samples were similar to those of uncoated samples. A facile synthetic route to thermoresponsive PEI- graft -POEGMA functionalised superparamagnetic magnetite nanoparticles is described.
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However these studies further highlighted that use of an appropriate solvent could reduce the free energy of dissociation thereby reducing the relative difference in BDFE between the ester and amide groups. A commercial branched PEI sample was functionalised by reaction with 2-bromo-2-methylpropanoyl bromide giving an amide macroinitiator suitable for the atom transfer radical polymerisation (ATRP) of oligo(ethylene glycol methyl ether) methacrylate. The resulting PEI- graft -POEGMA copolymers were characterised by SEC, FT-IR and 1 H and 13 C NMR spectroscopy. PEI- graft -POEGMA coated magnetite nanoparticles were synthesised by a basic aqueous co-precipitation method and were characterised by transmission electron microscopy, thermogravimetric analysis and vibrating sample magnetometry and dynamic light scattering. These copolymer coated magnetite nanoparticles were demonstrated to be effectively stabilised in an aqueous medium. 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The polymerisation of OEGMA from a model molecular amide demonstrated the feasibility of POEGMA synthesis under mild ATRP conditions (20 °C in ethanol) albeit with low initiator efficiencies. DFT studies suggest that the amide functionality is intrinsically of lower activity than ester functional monomers and initiators for atom transfer polymerisation (ATRP) as a consequence of higher bond dissociation energies and bond dissociation free energies (BDFE). However these studies further highlighted that use of an appropriate solvent could reduce the free energy of dissociation thereby reducing the relative difference in BDFE between the ester and amide groups. A commercial branched PEI sample was functionalised by reaction with 2-bromo-2-methylpropanoyl bromide giving an amide macroinitiator suitable for the atom transfer radical polymerisation (ATRP) of oligo(ethylene glycol methyl ether) methacrylate. 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title The polymerisation of oligo(ethylene glycol methyl ether) methacrylate from a multifunctional poly(ethylene imine) derived amide: a stabiliser for the synthesis and dispersion of magnetite nanoparticlesElectronic supplementary information (ESI) available: Plots of Cu(ii) function with time; UV-vis absorption spectra of Cu(i)Cl, Cu(ii)Cl2 and Cu(ii)Br2 solutions with DiMePiVA; X-ray diffraction pattern of PEI-graft-POEGMA stabilised nanoparticles; high magnification TEM images of magnetite nanopa
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