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Well-defined polymethylene-based block co/terpolymers by combining anthracene/maleimide diels–alder reaction with polyhomologation
Author(s) -
Nazeeha S. Alkayal,
Nikos Hadjichristidis
Publication year - 2015
Publication title -
polymer chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.403
H-Index - 117
eISSN - 1759-9962
pISSN - 1759-9954
DOI - 10.1039/c5py00601e
Subject(s) - maleimide , diels–alder reaction , anthracene , polymer chemistry , polyethylene glycol , ring opening polymerization , polymerization , chemistry , polycaprolactone , organic chemistry , catalysis , polymer
A novel strategy towards well-defined polymethylene-based co/terpolymers, by combining anthracene/maleimide Diels-Alder reaction with polyhomologation, is presented. For the synthesis of diblock copolymers the following approach was applied: a) synthesis of α-anthracene-ω-hydroxy- polymethylene by polyhomologation using tri (9-anthracene-methyl propyl ether) borane as initiator, b) synthesis of furan-protected-maleimide-terminated poly (ε-caprolactone) or polyethylene glycol and c). Diels-Alder reaction between the anthracene and maleimide-terminated polymers. In the case of triblock terpolymers the α-anthracene-ω-hydroxy-polymethylene was used as macroinitiator for the ring-opening polymerization of D, L-lactide to afford an anthracene-terminated PM-b-PLA copolymer, followed by Diels-Alder reaction with furan-protected maleimide-terminated poly (ε-caprolactone) or polyethylene glycol to give the triblock terpolymers. All intermediate and final products were characterized by SEC, 1H NMR, UV-VIS spectroscopy and DSC

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