SYNTHESIS OF pH-RESPONSIVE AMPHIPHILIC DIBLOCK COPOLYMERS CONTAINING POLYISOBUTYLENE via OXYANION-INITIATED POLYMERIZATION AND THEIR MULTIPLE SELF-ASSEMBLY MORPHOLOGIES
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SYNTHESIS OF pH-RESPONSIVE AMPHIPHILIC DIBLOCK COPOLYMERS CONTAINING POLYISOBUTYLENE via OXYANION-INITIATED POLYMERIZATION AND THEIR MULTIPLE SELF-ASSEMBLY MORPHOLOGIES
Chinese Journal of Polymer ScienceVol. 31, Issue 2, Pages: 218-231(2013)
Affiliations:
a.College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Jiangsu Key Laboratory of Advanced Functional Polymer Design and Application, Soochow University, Suzhou 215123, China
b.State Key Lab of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing 100029, China
Huai-chao Wang, Ming-zu Zhang, Pei-hong Ni, et al. SYNTHESIS OF pH-RESPONSIVE AMPHIPHILIC DIBLOCK COPOLYMERS CONTAINING POLYISOBUTYLENE via OXYANION-INITIATED POLYMERIZATION AND THEIR MULTIPLE SELF-ASSEMBLY MORPHOLOGIES[J]. Chinese Journal of Polymer Science, 2013, 31(2): 218-231. DOI: 10.1007/s10118-013-1208-9.
DOI:
Huai-chao Wang, Ming-zu Zhang, Pei-hong Ni, et al. SYNTHESIS OF pH-RESPONSIVE AMPHIPHILIC DIBLOCK COPOLYMERS CONTAINING POLYISOBUTYLENE via OXYANION-INITIATED POLYMERIZATION AND THEIR MULTIPLE SELF-ASSEMBLY MORPHOLOGIES[J]. Chinese Journal of Polymer Science, 2013, 31(2): 218-231. DOI: 10.1007/s10118-013-1208-9.DOI:
SYNTHESIS OF pH-RESPONSIVE AMPHIPHILIC DIBLOCK COPOLYMERS CONTAINING POLYISOBUTYLENE via OXYANION-INITIATED POLYMERIZATION AND THEIR MULTIPLE SELF-ASSEMBLY MORPHOLOGIES
and their multiple self-assembly behaviors have been studied. An exo-olefin-terminated highly reactive polyisobutylene (HRPIB) was first changed to hydroxyl-terminated PIB (PIB-OH)
via
hydroboration-oxidation of C=C double bond in the chain end
and then reacted with KH to yield a potassium alcoholate of PIB (PIB-O
−
K
+
). PIB-O
−
K
+
was immediately used as a macroinitiator to polymerize DMAEMA monomer
resulting in a cationic di
block
copolymer PIB-
b
-PDMAEMA. With the similar synthesis procedure
the anionic di
block
copolymer PIB-
b
- PMAA could be prepared
via
a combination of oxyanion-initiated polymerization of
tert
-butyl methacrylate (
t
BMA) and subsequent hydrolysis of
tert
-butyl ester groups in P
t
BMA
block
. The functional PIB and
block
copolymers have been fully characterized by
1
H-NMR
FT-IR spectroscopy
and gel permeation chromatography (GPC). These samples allowed us to systematically investigate the effects of
block
composition on the pH responsivity and various self-assembled morphologies of the copolymers in THF/water mixed solvent. Transmission electron microscopy (TEM) images revealed that these di
block
copolymers containing small amount of original PIB without exo-olefin-terminated group are able to self-assemble into micelles
vesicles with different particle sizes and cylindrical aggregates
depending on various factors including
block
copolymer composition
solvent polarity and pH value.
关键词
Keywords
references
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Sulfonated Poly(α-methyl styrene-b-isobutylene-b-α-methyl styrene) Copolymers for Advanced Proton Exchange Membranes
Phenols/Al(C6F5)3Initiation Systems for Cationic Polymerizations of Isobutylene
Biocompatible, Hemocompatible and Antibacterial Acylated Dextran-g-polyisobutylene Graft Copolymers with Silver Nanoparticles
Amphiphilic Graft Copolymers of Hydroxypropyl Cellulose Backbone with Nonpolar Polyisobutylene Branches
Special Topic: Chirality in Polymers
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Related Institution
State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology
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State Key Laboratory of Molecular Engineering of Polymers, Department of Macromolecular Science, Fudan University