Giant Vesicle Formation through Self-Assembly of Complementary Random Copolymers

2000 ◽  
Vol 122 (24) ◽  
pp. 5895-5896 ◽  
Author(s):  
Faysal Ilhan ◽  
Trent H. Galow ◽  
Mark Gray ◽  
Gilles Clavier ◽  
Vincent M. Rotello
Keyword(s):  
Self Assembly ◽  
Random Copolymers ◽  
Vesicle Formation ◽  
Giant Vesicle

Giant vesicle formation through self-assembly of chitooligosaccharide-based graft copolymers

2008 ◽  
pp. 1449 ◽  
Author(s):  
Ke-Jing Gao ◽  
Guangtao Li ◽  
Xinping Lu ◽  
Y. G. Wu ◽  
Bo-Qing Xu ◽  
...  
Keyword(s):  
Self Assembly ◽  
Graft Copolymers ◽  
Vesicle Formation ◽  
Giant Vesicle

Selective Vesicle Formation from Calixarenes by Self-Assembly

1999 ◽  
Vol 38 (4) ◽  
pp. 504-506 ◽  
Author(s):  
Yasutaka Tanaka ◽  
Masami Miyachi ◽  
Yoshiaki Kobuke
Keyword(s):  
Self Assembly ◽  
Vesicle Formation

Size-Defined Cracked Vesicle Formation via Self-Assembly of Gold Nanoparticles Covered with Carboxylic Acid-Terminated Surface Ligands

Langmuir ◽  
2018 ◽  
Vol 34 (41) ◽  
pp. 12445-12451 ◽  
Author(s):  
Jinjian Wei ◽  
Hideyuki Mitomo ◽  
Takeharu Tani ◽  
Yasutaka Matsuo ◽  
Kenichi Niikura ◽  
...  
Keyword(s):  
Gold Nanoparticles ◽  
Carboxylic Acid ◽  
Self Assembly ◽  
Vesicle Formation ◽  
Surface Ligands

Elementary approach to self-assembly in random copolymers

2000 ◽  
Vol 661 ◽  
Author(s):  
Shirish M. Chitanvis
Keyword(s):  
Self Assembly ◽  
Density Functional ◽  
Functional Integration ◽  
Time Dependent ◽  
Random Copolymers ◽  
Integration Time ◽  
Average Chain Length ◽  
Elementary Approach ◽  
Flexible Chain ◽  
Non Local

We have mapped the physics of a system of random copolymers onto a time-dependent density functional-type field theory using techniques of functional integration. Time in the theory is merely a label for the location of a given monomer along the extent of a flexible chain. We derive heuristically within this approach a non-local constraint which prevents segments on chains in the system from straying too far from each other, and leads to self-assembly. The structure factor is then computed in a straightforward fashion. The dependence of various calculated quantities on the average chain length are compared with experiments. The profile and size of spherulitic mesoscale domains is also computed.

Programmed Self-Assembly Systems of Amphiphilic Random Copolymers into Size-Controlled and Thermoresponsive Micelles in Water

2018 ◽  
Vol 51 (2) ◽  
pp. 398-409 ◽  
Author(s):  
Shota Imai ◽  
Yuji Hirai ◽  
Chitose Nagao ◽  
Mitsuo Sawamoto ◽  
Takaya Terashima
Keyword(s):  
Self Assembly ◽  
Random Copolymers ◽  
Assembly Systems ◽  
Size Controlled

Water dynamics and self-assembly of single-chain nanoparticles in concentrated solutions

Soft Matter ◽  
2020 ◽  
Vol 16 (42) ◽  
pp. 9738-9745
Author(s):  
Beatriz Robles-Hernández ◽  
Edurne González ◽  
José A. Pomposo ◽  
Juan Colmenero ◽  
Ángel Alegría
Keyword(s):  
Self Assembly ◽  
The Self ◽  
Water Dynamics ◽  
Nano Particles ◽  
Random Copolymers ◽  
Core Shell ◽  
Dielectric Studies ◽  
Single Chain ◽  
Concentrated Solutions ◽  
Overlap Concentration

Dielectric studies on water dynamics in aqueous solutions of amphiphilic random copolymers confirm the self-assembly into globular like core–shell single-chain nano-particles (SCNPs) at concentrations well above the overlap concentration.

Sign in / Sign up

Export Citation Format

Share Document