Issue 90, 2014

Magnetic composite nanoparticles consisting of helical poly(n-hexyl isocyanate) and Fe3O4 prepared via click reaction

Abstract

A novel type of magnetic composite particles was constructed using helical poly(n-hexyl isocyanate) and Fe3O4. For this purpose, well-defined 4-ethynylbenzyloxy-terminal poly(n-hexyl isocyanate)s (PHIC–C[triple bond, length as m-dash]Cs) were synthesized via coordination polymerization by using an organotitanium catalyst. The PHIC–C[triple bond, length as m-dash]Cs were characterized by GPC, FT-IR and 1H NMR techniques. UV-vis absorption spectra demonstrated that the PHIC–C[triple bond, length as m-dash]Cs adopted dynamic helical structures in tetrahydrofuran. Azide-modified magnetic Fe3O4 nanoparticles (Fe3O4@N3 NPs) were prepared through the reaction between 3-azidopropyltrimethoxysilane and oleic acid-coated magnetic Fe3O4 NPs. The obtained clickable PHIC–C[triple bond, length as m-dash]C and Fe3O4@N3 NPs were subjected to the Cu-catalyzed azide/alkyne cycloaddition for synthesizing the anticipated Fe3O4@PHIC composite NPs. FT-IR, TGA and TEM techniques confirmed the formation of the magnetic composite nanoparticles. UV-vis absorption spectra demonstrated that the PHIC chains coated on the magnetic Fe3O4 NPs adopted dynamic helical structures. XRD measurements revealed that coating PHIC chains on Fe3O4 nanoparticles did not change the phase properties of Fe3O4 nanoparticles. The Fe3O4@PHIC composite NPs showed a saturation magnetization of 17.8 emu g−1 and the expected rapid magnetic responsivity.

Graphical abstract: Magnetic composite nanoparticles consisting of helical poly(n-hexyl isocyanate) and Fe3O4 prepared via click reaction

Supplementary files

Article information

Article type
Paper
Submitted
23 Jul 2014
Accepted
19 Sep 2014
First published
19 Sep 2014

RSC Adv., 2014,4, 48796-48803

Magnetic composite nanoparticles consisting of helical poly(n-hexyl isocyanate) and Fe3O4 prepared via click reaction

X. Liu, R. Cheng, J. Deng and Y. Wu, RSC Adv., 2014, 4, 48796 DOI: 10.1039/C4RA07476A

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