scholarly journals The influence of the end-group on the chiral self-assembly of all-conjugated block copolymers

2017 ◽  
Vol 8 (37) ◽  
pp. 5666-5672 ◽  
Author(s):  
M.-P. Van Den Eede ◽  
A. Bedi ◽  
J. Delabie ◽  
J. De Winter ◽  
P. Gerbaux ◽  
...  

This research demonstrates the influence of the end-group on the self-assembly of conjugated polymers.

Polymers ◽  
2020 ◽  
Vol 13 (1) ◽  
pp. 110
Author(s):  
Lin-Lin Xiao ◽  
Xu Zhou ◽  
Kan Yue ◽  
Zi-Hao Guo

In the past two decades, conjugated polymers (CPs) have drawn great attention due to their excellent conductivity and charge mobility, rendering them broad applications in organic electronics. Controlling over the morphologies and nanostructures of CPs is very important to improve the performance of CP-based devices, which is still a tremendously difficult task. Conjugated block copolymers (cBCPs), composed of different CP blocks or CP coupled with coiled polymeric blocks, not only maintain the advantages of high conductivity and mobility but also demonstrate features of morphological versatility and tunability. Due to the strong π–π interaction and crystallinity of the conjugated backbones, the self-assembly behaviors of cBCPs are very complicated and largely remain to be explored. In this tutorial review, we first summarize the general synthetic methods for different types of cBCPs. Then, recent studies on the self-assembly behaviors of cBCPs are discussed, with an emphasis on the structural factors that affect the morphologies of cBCPs both in bulk and thin film states. Finally, we briefly provide our outlook on the future research of the self-assembly of cBCPs.


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.


2010 ◽  
Vol 28 (2) ◽  
pp. 84-92 ◽  
Author(s):  
Jieshu Qian ◽  
Meng Zhang ◽  
Ian Manners ◽  
Mitchell A. Winnik

Nano Letters ◽  
2011 ◽  
Vol 11 (3) ◽  
pp. 998-1001 ◽  
Author(s):  
Justin Bolton ◽  
Travis S. Bailey ◽  
Javid Rzayev

Molecules ◽  
2019 ◽  
Vol 24 (9) ◽  
pp. 1772 ◽  
Author(s):  
Maria de los Angeles Cortes ◽  
Raquel de la Campa ◽  
Maria Luisa Valenzuela ◽  
Carlos Díaz ◽  
Gabino A. Carriedo ◽  
...  

During the last number of years a variety of crystallization-driven self-assembly (CDSA) processes based on semicrystalline block copolymers have been developed to prepare a number of different nanomorphologies in solution (micelles). We herein present a convenient synthetic methodology combining: (i) The anionic polymerization of 2-vinylpyridine initiated by organolithium functionalized phosphane initiators; (ii) the cationic polymerization of iminophosphoranes initiated by –PR2Cl2; and (iii) a macromolecular nucleophilic substitution step, to prepare the novel block copolymers poly(bistrifluoroethoxy phosphazene)-b-poly(2-vinylpyridine) (PTFEP-b-P2VP), having semicrystalline PTFEP core forming blocks. The self-assembly of these materials in mixtures of THF (tetrahydrofuran) and 2-propanol (selective solvent to P2VP), lead to a variety of cylindrical micelles of different lengths depending on the amount of 2-propanol added. We demonstrated that the crystallization of the PTFEP at the core of the micelles is the main factor controlling the self-assembly processes. The presence of pyridinyl moieties at the corona of the micelles was exploited to stabilize gold nanoparticles (AuNPs).


Langmuir ◽  
2003 ◽  
Vol 19 (21) ◽  
pp. 8625-8628 ◽  
Author(s):  
Maksudul M. Alam ◽  
Yan Zhu ◽  
Samson A. Jenekhe

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