TY - JOUR
T1 - Facile synthesis of multiblock copolymers composed of poly(tetramethylene oxide) and polystyrene using living free-radical polymerization macroinitiator
AU - Higaki, Yuji
AU - Otsuka, Hideyuki
AU - Takahara, Atsushi
N1 - Funding Information:
The authors gratefully acknowledge the financial support of Nissan Science Foundation, Shiseido Fund for Science and Technology, Research Foundation Materials Science, and a Grant-in-Aid for Scientific Research (14750699) from the Ministry of Education, Culture, Science, Sports and Technology of Japan. The present work is also supported by a Grant-in-Aid for the 21st Century COE Program, ‘Functional Innovation of Molecular Informatics’ from the Ministry of Education, Culture, Science, Sports and Technology of Japan. Y.H. acknowledges the financial support of Grant-in-Aid for JSPS Fellows.
PY - 2006/5/17
Y1 - 2006/5/17
N2 - A facile synthetic strategy for well-defined multiblock copolymers utilizing 'living' free-radical polymerization macroinitiator has been presented. Polyurethane composed of alkoxyamine initiating units and poly(tetramethylene oxide) (PTMO) segments was prepared by polyaddition of tolylene 2,4-diisocyanate terminated PTMO with an alkoxyamine-based diol. Polymerization of styrene with the polyurethane macroinitiator was carried out under nitroxide-mediated free-radical polymerization (NMRP) condition. GPC, NMR, and IR data revealed that the polymerization was accurately controlled and well-defined polystyrene chains were inserted in the main chain of macroinitiator to give the poly(tetramethylene oxide)-b-polystyrene multiblock copolymers. The synthesized multiblock copolymers were characterized by tensile test, differential scanning calorimetry, and dynamic mechanical analysis. Mechanical properties of the multiblock copolymers can be tuned by the sufficient molecular weight control of PS chains. Soft segment of PTMO and hard segment of PS were apparently compatible due to the multiblock structure of low molecular weight segments and polar urethane groups.
AB - A facile synthetic strategy for well-defined multiblock copolymers utilizing 'living' free-radical polymerization macroinitiator has been presented. Polyurethane composed of alkoxyamine initiating units and poly(tetramethylene oxide) (PTMO) segments was prepared by polyaddition of tolylene 2,4-diisocyanate terminated PTMO with an alkoxyamine-based diol. Polymerization of styrene with the polyurethane macroinitiator was carried out under nitroxide-mediated free-radical polymerization (NMRP) condition. GPC, NMR, and IR data revealed that the polymerization was accurately controlled and well-defined polystyrene chains were inserted in the main chain of macroinitiator to give the poly(tetramethylene oxide)-b-polystyrene multiblock copolymers. The synthesized multiblock copolymers were characterized by tensile test, differential scanning calorimetry, and dynamic mechanical analysis. Mechanical properties of the multiblock copolymers can be tuned by the sufficient molecular weight control of PS chains. Soft segment of PTMO and hard segment of PS were apparently compatible due to the multiblock structure of low molecular weight segments and polar urethane groups.
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U2 - 10.1016/j.polymer.2006.03.100
DO - 10.1016/j.polymer.2006.03.100
M3 - Article
AN - SCOPUS:33646807502
SN - 0032-3861
VL - 47
SP - 3784
EP - 3791
JO - Polymer
JF - Polymer
IS - 11
ER -