Polymerization-induced self-assembly of PVAc-b-PVDF block copolymers via RAFT dispersion polymerization of vinylidene fluoride in dimethyl carbonate

2017 ◽  
Vol 8 (9) ◽  
pp. 1477-1487 ◽  
Author(s):  
Marc Guerre ◽  
Mona Semsarilar ◽  
Franck Godiard ◽  
Bruno Améduri ◽  
Vincent Ladmiral

This article reports the results of the study of the RAFT dispersion polymerization of VDF in dimethyl carbonate using PVAc macroCTAs. The morphology of the resulting crystalline polymer aggregates is likely governed by crystallization of the PVDF.

2017 ◽  
Vol 8 (34) ◽  
pp. 5203-5211 ◽  
Author(s):  
Marc Guerre ◽  
Mona Semsarilar ◽  
Cedric Totée ◽  
Gilles Silly ◽  
Bruno Améduri ◽  
...  

Self-assembly of PDMAEMA-b-PVDF block copolymers.


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.


2002 ◽  
Vol 724 ◽  
Author(s):  
Elizabeth R. Wright ◽  
R. Andrew McMillan ◽  
Alan Cooper ◽  
Robert P. Apkarian ◽  
Vincent P. Conticello

AbstractTriblock copolymers have traditionally been synthesized with conventional organic components. However, triblock copolymers could be synthesized by the incorporation of two incompatible protein-based polymers. The polypeptides would differ in their hydrophobicity and confer unique physiochemical properties to the resultant materials. One protein-based polymer, based on a sequence of native elastin, that has been utilized in the synthesis of biomaterials is poly (Valine-Proline-Glycine-ValineGlycine) or poly(VPGVG) [1]. This polypeptide has been shown to have an inverse temperature transition that can be adjusted by non-conservative amino acid substitutions in the fourth position [2]. By combining polypeptide blocks with different inverse temperature transition values due to hydrophobicity differences, we expect to produce amphiphilic polypeptides capable of self-assembly into hydrogels. Our research examines the design, synthesis and characterization of elastin-mimetic block copolymers as functional biomaterials. The methods that are used for the characterization include variable temperature 1D and 2D High-Resolution-NMR, cryo-High Resolutions Scanning Electron Microscopy and Differential Scanning Calorimetry.


Author(s):  
Weihua Li ◽  
Xueying Gu

Since tremendous progress has been made, directed self-assembly (DSA) of block copolymers has been regarded as one of the most promising bottom-up lithography techniques. In particular, DSA has been successfully...


2020 ◽  
Vol 2 (11) ◽  
pp. 4893-4901
Author(s):  
Karthika Madathil ◽  
Kayla A. Lantz ◽  
Morgan Stefik ◽  
Gila E. Stein

2021 ◽  
Author(s):  
Wei Wen ◽  
Aihua Chen

Self-assembly of amphiphilic single chain Janus nanoparticles (SCJNPs) is a novel and promising approach to fabricate assemblies with diversified morphologies. However, the experimental research of the self-assembly behavior of SCJNPs...


Soft Matter ◽  
2021 ◽  
Author(s):  
Alexander Kantardjiev

We carried out a series of coarse-grained molecular dynamics liposome-copolymer simulations with varying extent of copolymer concentration in an attempt to understand the effect of copolymer structure and concentration on vesicle self-assembly and stability.


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