Synthesis of Homopolymers, Diblock Copolymers, and Multiblock Polymers by Organocatalyzed Group Transfer Polymerization of Various Acrylate Monomers

2015 ◽  
Vol 48 (3) ◽  
pp. 511-519 ◽  
Author(s):  
Kenji Takada ◽  
Takahiro Ito ◽  
Kodai Kitano ◽  
Shinji Tsuchida ◽  
Yu Takagi ◽  
...  
Keyword(s):  
Diblock Copolymers ◽  
Group Transfer ◽  
Acrylate Monomers

Synthesis and Characterization of Branched Water-Soluble Homopolymers and Diblock Copolymers Using Group Transfer Polymerization

2005 ◽  
Vol 38 (12) ◽  
pp. 4977-4982 ◽  
Author(s):  
V. Bütün ◽  
I. Bannister ◽  
N. C. Billingham ◽  
D. C. Sherrington ◽  
S. P. Armes
Keyword(s):  
Diblock Copolymers ◽  
Water Soluble ◽  
Synthesis And Characterization ◽  
Group Transfer

Controlled Thioacyl Group Transfer (TAGT) Polymerization of Cyclic Sulfide:  Novel Approach to AB Diblock Copolymers by the Combination of RAFT and TAGT Polymerizations

2007 ◽  
Vol 40 (23) ◽  
pp. 8129-8131 ◽  
Author(s):  
Atsushi Nagai ◽  
Naoyuki Koike ◽  
Hiroto Kudo ◽  
Tadatomi Nishikubo
Keyword(s):  
Diblock Copolymers ◽  
Group Transfer ◽  
Novel Approach ◽  
Cyclic Sulfide

scholarly journals Organic acids as efficient catalysts for group transfer polymerization of N,N-disubstituted acrylamide with silyl ketene acetal: polymerization mechanism and synthesis of diblock copolymers

2015 ◽  
Vol 6 (38) ◽  
pp. 6845-6856 ◽  
Author(s):  
Seiya Kikuchi ◽  
Yougen Chen ◽  
Kodai Kitano ◽  
Kenji Takada ◽  
Toshifumi Satoh ◽  
...  
Keyword(s):  
Organic Acids ◽  
Organic Acid ◽  
Diblock Copolymers ◽  
Polymerization Mechanism ◽  
Group Transfer ◽  
Ketene Acetal

The GTP of N,N-disubstituted acrylamide using organic acid and silyl ketene acetal was intensively investigated.

Surface active semifluorinated diblock copolymers prepared by group transfer polymerization

1996 ◽  
Vol 102 (1) ◽  
pp. 99-106 ◽  
Author(s):  
Maarten J. Krupers ◽  
Fernando M. E. Cabelo ◽  
Martin Möller
Keyword(s):  
Diblock Copolymers ◽  
Group Transfer ◽  
Surface Active

Morphological behavior of compatibilized ternary blends prepared by mechanical mixing

1993 ◽  
Vol 51 ◽  
pp. 1200-1201
Author(s):  
S.D. Smith ◽  
R.J. Spontak ◽  
D.H. Melik ◽  
S.M. Buehler ◽  
K.M. Kerr ◽  
...  
Keyword(s):  
Interfacial Adhesion ◽  
Diblock Copolymers ◽  
Ternary Blends ◽  
Mechanical Mixing ◽  
Design Considerations ◽  
Covalently Bonded ◽  
Homopolymer Blends ◽  
Emulsifying Agent ◽  
Surface Active ◽  
Low Entropy

When blended together, homopolymers A and B will normally macrophase-separate into relatively large (≫1 μm) A-rich and B-rich phases, between which exists poor interfacial adhesion, due to a low entropy of mixing. The size scale of phase separation in such a blend can be reduced, and the extent of interfacial A-B contact and entanglement enhanced, via addition of an emulsifying agent such as an AB diblock copolymer. Diblock copolymers consist of a long sequence of A monomers covalently bonded to a long sequence of B monomers. These materials are surface-active and decrease interfacial tension between immiscible phases much in the same way as do small-molecule surfactants. Previous studies have clearly demonstrated the utility of block copolymers in compatibilizing homopolymer blends and enhancing blend properties such as fracture toughness. It is now recognized that optimization of emulsified ternary blends relies upon design considerations such as sufficient block penetration into a macrophase (to avoid block slip) and prevention of a copolymer multilayer at the A-B interface (to avoid intralayer failure).

Triply-periodic nanostructures in surfactant, block copolymer, and biomembrane systems, and simulation of TEMs

1993 ◽  
Vol 51 ◽  
pp. 884-885
Author(s):  
David M. Anderson ◽  
Tomas Landh
Keyword(s):  
Liquid Crystalline ◽  
Diblock Copolymers ◽  
Cubic Phase ◽  
List Type ◽  
Interpenetrating Networks ◽  
Triply Periodic ◽  
Wide Range ◽  
Bicontinuous Cubic ◽  
Phase Liquid ◽  
Dividing Surface

First discovered in surfactant-water liquid crystalline systems, so-called ‘bicontinuous cubic phases’ have the property that hydropnilic and lipophilic microdomains form interpenetrating networks conforming to cubic lattices on the scale of nanometers. Later these same structures were found in star diblock copolymers, where the simultaneous continuity of elastomeric and glassy domains gives rise to unique physical properties. Today it is well-established that the symmetry and topology of such a morphology are accurately described by one of several triply-periodic minimal surfaces, and that the interface between hydrophilic and hydrophobic, or immiscible polymer, domains is described by a triply-periodic surface of constant, nonzero mean curvature. One example of such a dividing surface is shown in figure 5.The study of these structures has become of increasing importance in the past five years for two reasons:1)Bicontinuous cubic phase liquid crystals are now being polymerized to create microporous materials with monodispersed pores and readily functionalizable porewalls; figure 3 shows a TEM from a polymerized surfactant / methylmethacrylate / water cubic phase; and2)Compelling evidence has been found that these same morphologies describe biomembrane systems in a wide range of cells.

Equilibrium emulsification of polymer blends by diblock copolymers

1990 ◽  
Vol 51 (2) ◽  
pp. 185-200 ◽  
Author(s):  
Zhen-Gang Wang ◽  
S.A. Safran
Keyword(s):  
Polymer Blends ◽  
Diblock Copolymers

Mechanical and Structural Consequences of Associative Dynamic Cross-Linking in Acrylic Diblock Copolymers

2019 ◽  
Author(s):  
Jacob Ishibashi ◽  
Yan Fang ◽  
Julia Kalow
Keyword(s):  
Block Copolymers ◽  
Rheological Properties ◽  
Diblock Copolymers ◽  
Cross Linking ◽  
Statistical Copolymer

<p>Block copolymers are used to construct covalent adaptable networks that employ associative exchange chemistry (vitrimers). The resulting vitrimers display markedly different nanostructural, thermal and rheological properties relative to those of their statistical copolymer-derived counterparts. This study demonstrates that prepolymer sequence is a versatile strategy to modify the properties of vitrimers.</p>

Multi-Stimuli-Responsive Mesoporous Membranes and Effect of Molecular Architecture on Thermo- and pH-Responsive Behavior of the grafted Block Copolymer brushes

2019 ◽  
Author(s):  
Yanchun Tang ◽  
Kohzo Ito ◽  
Hideaki Yokoyama
Keyword(s):  
Polymer Brushes ◽  
Diblock Copolymers ◽  
Neutron Reflectivity ◽  
Molecular Architecture ◽  
Stimuli Responsive ◽  
Responsive Polymer ◽  
The Matrix ◽  
Stable Part ◽  
Copolymer Brushes ◽  
Mesoporous Membranes

In this study, we prepared ultrafiltration membranes with a decoupled responses of filtration property to temperature and pH. The membrane preparation method was developed based on our previous work. We utilized methanol-supercritical carbon dioxide (methanol-scCO<sub>2</sub>) selective swelling method to introduce nanopores to block copolymers containing poly(diethylene glycol) methyl ether methacrylate (PMEO<sub>2</sub>MA), poly(N,N-dimethylaminoethyl methacrylate) (PDMAEMA) and polystyrene (PS) blocks. Formation of the mesoporous barrier layer with PS being the mechanically stable part of the matrix was driven by selective swelling of the PMEO<sub>2</sub>MA-b-PDMAEMA domains. Due to the selective swelling of PMEO<sub>2</sub>MA or PDMAEMA domains to introduce pores, the interior of the pores are covered with PMEO<sub>2</sub>MA or PDMAEMA blocks after pore formation. The PMEO<sub>2</sub>MA-b-PDMAEMA polymer brushes are naturally attached on the pore walls and worked as functional gates. PMEO<sub>2</sub>MA is a non-toxic, neutral thermo-responsive polymer with LCST at 26 ᴼC. PDMAEMA is a typical weak polyelectrolyte with pK<sub>a</sub> value at 7.0-7.5 and also a thermo-responsive polymer revealed a LCST of 20-80 °C in aqueous solution. Therefore, these membranes were expected to have multi dimensions as function of the combination of temperature and pH. Moreover, to understand the detail of the temperature and pH depended conformation transitions of PMEO<sub>2</sub>MA-b-PDMAEMA brushes, those diblock copolymers were end-tethered on flat substrates and analyzed via neutron reflectivity (NR).

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