Reversible Morphological Evolution of Responsive Giant Vesicles to Nanospheres by the Self-Assembly of Crystalline-b -Coil Polyphosphazene Block Copolymers

2016 ◽  
Vol 22 (13) ◽  
pp. 4483-4491 ◽  
Author(s):  
Silvia Suárez-Suárez ◽  
Gabino A. Carriedo ◽  
Alejandro Presa Soto
Keyword(s):  
Block Copolymers ◽  
Self Assembly ◽  
Morphological Evolution ◽  
The Self ◽  
Giant Vesicles

Porous films by the self-assembly of inorganic rod-b-coil block copolymers: mechanistic insights into the vesicle-to-pore morphological evolution

Soft Matter ◽  
2016 ◽  
Vol 12 (12) ◽  
pp. 3084-3092 ◽  
Author(s):  
Silvia Suárez-Suárez ◽  
Gabino A. Carriedo ◽  
Alejandro Presa Soto
Keyword(s):  
Thin Films ◽  
Block Copolymers ◽  
Self Assembly ◽  
Morphological Evolution ◽  
The Self ◽  
Porous Films ◽  
Spontaneous Formation

The self-assembly in thin films of polyphosphazene block copolymers combining a rigid ([N = P(O2C12H8)], O2C12H8= 2,2′-dioxy-1,1′-biphenyl) and a flexible ([N = PMePh]) blocks, led to the spontaneous formation of porous films through a vesicle-to-pore morphological evolutions pathway.

Self-Assembly of Single Chain Janus Nanoparticles from Azobenzene-Containing Block Copolymers and Reversible Photoinduced Morphology Transition

2021 ◽  
Author(s):  
Wei Wen ◽  
Aihua Chen
Keyword(s):  
Block Copolymers ◽  
Experimental Research ◽  
Self Assembly ◽  
The Self ◽  
Single Chain ◽  
Morphology Transition ◽  
Janus Nanoparticles ◽  
Assembly Behavior

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...

Coarse-grained simulation of the self-assembly of lipid vesicles concomitantly with novel block copolymers with multiple tails

Soft Matter ◽  
2021 ◽  
Author(s):  
Alexander Kantardjiev
Keyword(s):  
Molecular Dynamics ◽  
Block Copolymers ◽  
Self Assembly ◽  
Lipid Vesicles ◽  
The Self ◽  
Coarse Grained ◽  
Copolymer Concentration ◽  
Copolymer Structure ◽  
Coarse Grained Molecular Dynamics

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.

Nanofiber micelles from the self-assembly of block copolymers

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

Large Pore Size Nanoporous Materials from the Self-Assembly of Asymmetric Bottlebrush Block Copolymers

Nano Letters ◽  
2011 ◽  
Vol 11 (3) ◽  
pp. 998-1001 ◽  
Author(s):  
Justin Bolton ◽  
Travis S. Bailey ◽  
Javid Rzayev
Keyword(s):  
Block Copolymers ◽  
Pore Size ◽  
Self Assembly ◽  
Nanoporous Materials ◽  
The Self ◽  
Large Pore ◽  
Large Pore Size

scholarly journals Cylindrical Micelles by the Self-Assembly of Crystalline-b-Coil Polyphosphazene-b-P2VP Block Copolymers. Stabilization of Gold Nanoparticles

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 ◽  
...  
Keyword(s):  
Gold Nanoparticles ◽  
Block Copolymers ◽  
Self Assembly ◽  
Cationic Polymerization ◽  
The Self ◽  
The Novel ◽  
Selective Solvent ◽  
The Core ◽  
Cylindrical Micelles ◽  
Main Factor

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).

Circular Nanopatterns over Large Areas from the Self-Assembly of Block Copolymers Guided by Shallow Trenches

ACS Nano ◽  
2011 ◽  
Vol 5 (4) ◽  
pp. 2855-2860 ◽  
Author(s):  
Sung Woo Hong ◽  
Xiaodan Gu ◽  
June Huh ◽  
Shuaigang Xiao ◽  
Thomas P. Russell
Keyword(s):  
Block Copolymers ◽  
Self Assembly ◽  
The Self
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