TY - JOUR
T1 - Synthesis of aromatic oxazolyl- and carboxyl-functionalized polymers: Atom transfer radical polymerization of styrene initiated by 2-[(4-bromomethyl) phenyl]-4,5-dihydro-4,4-dimethyloxazole
AU - Summers, Gabriel J.
AU - Maseko, Rejoice B.
AU - Beebeejaun, B. M.Parveen
AU - Summers, Carol A.
PY - 2011/6/15
Y1 - 2011/6/15
N2 - The synthesis of a new compound, 2-[(4-bromomethyl)phenyl]-4,5-dihydro-4,4- dimethyloxazole (1), and its utility in the synthesis of oxazoline- functionalized polystyrene by atom transfer radical polymerization (ATRP) methods are described. Aromatic oxazolyl-functionalized polymers were prepared by the ATRP of styrene, initiated by (1) in the presence of copper(I) bromide/2,2′-bipyridyl catalyst system, to afford the corresponding α-oxazolyl-functionalized polystyrene (2). The polymerization proceeded via a controlled free radical polymerization process to produce the corresponding α-oxazolyl-functionalized polymers with predictable number-average molecular weights, narrow molecular weight distributions in high-initiator efficiency reactions. Post-ATRP chain end modification of α-oxazolyl-functionalized polystyrene (2) to form the corresponding α-carboxyl-functionalized polystyrene (3) was achieved by successive acid-catalyzed hydrolysis and saponification reactions. The polymerization processes were monitored by gas chromatography analyses. The unimolecular-functionalized initiator and functionalized polymers were characterized by thin layer chromatography, spectroscopy, size exclusion chromatography, and nonaqueous titration analysis. © 2011 Wiley Periodicals, Inc.
AB - The synthesis of a new compound, 2-[(4-bromomethyl)phenyl]-4,5-dihydro-4,4- dimethyloxazole (1), and its utility in the synthesis of oxazoline- functionalized polystyrene by atom transfer radical polymerization (ATRP) methods are described. Aromatic oxazolyl-functionalized polymers were prepared by the ATRP of styrene, initiated by (1) in the presence of copper(I) bromide/2,2′-bipyridyl catalyst system, to afford the corresponding α-oxazolyl-functionalized polystyrene (2). The polymerization proceeded via a controlled free radical polymerization process to produce the corresponding α-oxazolyl-functionalized polymers with predictable number-average molecular weights, narrow molecular weight distributions in high-initiator efficiency reactions. Post-ATRP chain end modification of α-oxazolyl-functionalized polystyrene (2) to form the corresponding α-carboxyl-functionalized polystyrene (3) was achieved by successive acid-catalyzed hydrolysis and saponification reactions. The polymerization processes were monitored by gas chromatography analyses. The unimolecular-functionalized initiator and functionalized polymers were characterized by thin layer chromatography, spectroscopy, size exclusion chromatography, and nonaqueous titration analysis. © 2011 Wiley Periodicals, Inc.
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U2 - 10.1002/pola.24692
DO - 10.1002/pola.24692
M3 - Article
SN - 0887-624X
SP - 2601
EP - 2614
JO - Journal of Polymer Science, Part A: Polymer Chemistry
JF - Journal of Polymer Science, Part A: Polymer Chemistry
ER -