Synthesis and Solution-state Assembly or Bulk State Thiol-ene Crosslinking of Pyrrolidinone- and Alkene-functionalized Amphiphilic Block Fluorocopolymers: From Functional Nanoparticles to Anti-fouling Coatings

2010 ◽  
Vol 63 (8) ◽  
pp. 1159 ◽  
Author(s):  
Jun Ma ◽  
Jeremy W. Bartels ◽  
Zhou Li ◽  
Ke Zhang ◽  
Chong Cheng ◽  
...  

With an ever increasing interest in the combined functionality and versatility of materials, increasing demands are placed on synthetic methodologies by which to produce such materials. This work demonstrates the preparation of block copolymers having fluorocarbon content, pyrrolidinone units, and alkene groups as complex building blocks for the assembly of discrete nanoparticles in solution and, alternatively, transformation into sophisticated crosslinked networks. Reversible addition–fragmentation chain transfer (RAFT) polymerization is a facile tool for the synthesis of well-defined polymers containing imbedded side-chain functionalities. In this work, the synthesis of well-defined multifunctional fluorinated polymers bearing pendant pyrrolidinone groups, and block copolymers bearing both pyrrolidinone and alkenyl groups on different segments was achieved, by using RAFT polymerizations of unique bifunctional monomers. Upon micellization, the amphiphilic diblock copolymers were transformed into regioselectively-functionalized nanoparticles. Further transformations of pyrrolidinone- and alkene-dual functionalized-block copolymers into complex amphiphilic networks were accomplished by highly efficient UV-induced thiol-ene reactions. Whether as discrete nanoparticles or nanoscopically-segregated crosslinked networks, these materials have great potential for several diverse technologies, including as anti-fouling materials.

2021 ◽  
Author(s):  
Enrique Folgado ◽  
Matthias Mayor ◽  
Didier Cot ◽  
Michel Ramonda ◽  
Franck Godiard ◽  
...  

PNIPAM-b-PVDF amphiphilic block copolymers were synthesized via RAFT polymerization in dimethyl carbonate. These block copolymers were able to self-assemble into various morphologies such as spherical, crumpled, lamellar and lenticular 2D aggregates.


2021 ◽  
Author(s):  
Peter Černoch ◽  
Alessandro Jäger ◽  
Zulfia Cernochova ◽  
Vladimir Sincari ◽  
Lindomar Calumby Albuquerque ◽  
...  

A two-step synthetic approach via the combination of living cationic ring-opening (CROP) and reversible addition-fragmentation chain transfer (RAFT) polymerization techniques was used to produce novel amphiphilic block copolymers based on...


2019 ◽  
Vol 484 (4) ◽  
pp. 431-435
Author(s):  
K. E. Chekurov ◽  
A. I. Barabanova ◽  
I. V. Blagodatskikh ◽  
B. V. Lokshin ◽  
A. S. Peregudov ◽  
...  

Amphiphilic diblock-copolymers (DC) of (2,3,4,5,6)-pentafluorostyrene and 2-hydroxyethyl methacrylate were prepared for the first time by two-step reversible addition–fragmentation chain transfer (RAFT) polymerization. The morphology of films of diblock-copolymers that have a composition close to equimolar was studied by transmission electron microscopy. The observed microphase separation and formation of spherical nanodomains is not typical for equimolar diblock-copolymers and seems to result from hydrogen bonding between the hydroxyl and carbonyl groups (OH···OH and C=O···HO) in poly(2-hydroxyethyl methacrylate) blocks. Obviously, it is the ability of diblock-copolymers to self-organization is the cause of formation of fabric coatings with low surface energy (γ = 11.9 mJ/m2) and relatively large water contact angles (θН2О = 120±6°) and diiodmetane (θCH2I2 = 93±2°).


2021 ◽  
Author(s):  
Tingyu He ◽  
Atsushi Narumi ◽  
Yanqiu Wang ◽  
Liang Xu ◽  
Shin-ichiro Sato ◽  
...  

A synthetic method for a series of poly(glycidol) (PG)-based amphiphilic block copolymers is presented with an emphasis on the catalyst switch method from an organic superbase (t-Bu-P4) to another with...


2015 ◽  
Vol 6 (12) ◽  
pp. 2274-2282 ◽  
Author(s):  
Weiwei Zhang ◽  
Weiwei Jiang ◽  
Delong Zhang ◽  
Guangyue Bai ◽  
Pengxiao Lou ◽  
...  

Two new amphiphilic linear-dendritic block copolymers have been synthesized and characterized. And their association behaviors have also been studied.


Polymers ◽  
2020 ◽  
Vol 12 (2) ◽  
pp. 487
Author(s):  
Yusheng Liu ◽  
Yigang Liu ◽  
Qiuxia Wang ◽  
Yugui Han ◽  
Hao Chen ◽  
...  

The incorporation of double dynamic bonds into hydrogels provides an effective strategy to engineer their performance on demand. Herein, novel hydrogels were PREPARED by combining two kinetically distinct dynamic covalent bonds, boronate ester and acylhydrazone bonds, and the synergistic properties of the hydrogels were studied comprehensively. The functional diblock copolymers P(N-isopropyl acrylamide-co-N-acryloyl-3-aminophenylboronic acid)-b-(N-isopropyl acrylamide-co-diacetone acrylamide) (PAD) were prepared via reversible addition−fragmentation chain transfer (RAFT) polymerization. The hydrogel was constructed by exploiting dynamic reaction of phenyboronic acid moieties with polyvinyl alcohol (PVA) and ketone moieties with adipic dihydrazide (ADH) without any catalyst. The active boronate ester linkage endows the hydrogel with fast gelation kinetics and self-healing ability, and the stable acylhydrazone linkage can enhance the mechanical property of the hydrogel. The difference in kinetics endows that the contribution of each linkage to mechanical strength of the hydrogel can be accurately estimated. Moreover, the mechanical property of the hydrogel can be readily engineered by changing the composition and solid content, as well as by controlling the formation or dissociation of the dynamic linkages. Thus, we provide a promising strategy to design and prepare multi-responsive hydrogels with tunable properties.


Molecules ◽  
2020 ◽  
Vol 25 (21) ◽  
pp. 5147
Author(s):  
Wanting Hou ◽  
Ruiqi Liu ◽  
Siwei Bi ◽  
Qian He ◽  
Haibo Wang ◽  
...  

Due to a strong retardation effect of o-nitrobenzyl ester on polymerization, it is still a great challenge to prepare amphiphilic block copolymers for polymersomes with a o-nitrobenzyl ester-based hydrophobic block. Herein, we present one such solution to prepare amphiphilic block copolymers with pure poly (o-nitrobenzyl acrylate) (PNBA) as the hydrophobic block and poly (N,N’-dimethylacrylamide) (PDMA) as the hydrophilic block using bulk reversible addition-fragmentation chain transfer (RAFT) polymerization of o-nitrobenzyl acrylate using a PDMA macro-RAFT agent. The developed amphiphilic block copolymers have a suitable hydrophobic/hydrophilic ratio and can self-assemble into photoresponsive polymersomes for co-loading hydrophobic and hydrophilic cargos into hydrophobic membranes and aqueous compartments of the polymersomes. The polymersomes demonstrate a clear photo-responsive characteristic. Exposure to light irradiation at 365 nm can trigger a photocleavage reaction of o-nitrobenzyl groups, which results in dissociation of the polymersomes with simultaneous co-release of hydrophilic and hydrophobic cargoes on demand. Therefore, these polymersomes have great potential as a smart drug delivery nanocarrier for controllable loading and releasing of hydrophilic and hydrophobic drug molecules. Moreover, taking advantage of the conditional releasing of hydrophilic and hydrophobic drugs, the drug delivery system has potential use in medical applications such as cancer therapy.


2003 ◽  
Vol 36 (11) ◽  
pp. 4208-4215 ◽  
Author(s):  
Shin-ichi Yusa ◽  
Yoshihiko Shimada ◽  
Yoshiro Mitsukami ◽  
Tohei Yamamoto ◽  
Yotaro Morishima

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