Multireactive Poly(2-oxazoline) Nanofibers through Electrospinning with Crosslinking on the Fly
Author(s) -
Ozlem Ipek Kalaoglu-Altan,
Bart Verbraeken,
Kathleen Lava,
Tuğçe Nihal Gevrek,
Rana Sanyal,
Tim R. Dargaville,
Karen De Clerck,
Richard Hoogenboom,
Amitav Sanyal
Publication year - 2016
Publication title -
acs macro letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.966
H-Index - 92
ISSN - 2161-1653
DOI - 10.1021/acsmacrolett.6b00188
Subject(s) - alkene , thiol , nanofiber , polymer chemistry , oxazoline , materials science , electrospinning , copolymer , ene reaction , maleimide , polymer , chemistry , organic chemistry , nanotechnology , catalysis , composite material
Crosslinked hydrophilic poly(2-oxazoline)-based nanofibers amenable to facile multi-functionalization are fabricated using alkene-containing poly(2-alkyl-2-oxazoline)s (PAOx) via in situ photo-initiated radical thiol-ene conjugation during electrospinning. The resulting crosslinked nanofibers are demonstrated to be multi-functionalizable using different chemistries as they contain two functional handles, being the alkene moieties from the parent copolymer and the residual thiol groups from the tetra-thiol based crosslinker. While the thiol groups in these nanofibers could be passivated or conjugated to install functional molecules through thiol-maleimide conjugation, the alkene groups could sequentially be modified with thiol-containing molecules using photo-initiated radical thiol-ene reactions. Utilization of the photochemically induced conjugation of thiol-bearing molecules to the alkene groups on the nanofibers is used to obtain functionalization in a spatially controlled manner
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