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Dissipative self-assembly of a dual-responsive block copolymer driven by a chemical oscillator.

Authors :
Li, Xuewei
Wang, Guangtong
Zhang, Qianqian
Liu, Yang
Sun, Tiedong
Liu, Shaoqin
Source :
Journal of Colloid & Interface Science. Jun2022, Vol. 615, p732-739. 8p.
Publication Year :
2022

Abstract

[Display omitted] Coupling stimuli-responsive building blocks with an oscillating reaction is an effective strategy to realize and investigate dissipative self-assembly. More importantly, since there is usually more than one component of which concentration periodically changes in a chemical oscillator, it can be expected that this strategy has the advantage of achieving dissipative self-assembly of the building blocks with dual- or even multi-responsiveness. We realized the dissipative self-assembly of a pH- and iodine-responsive block copolymer, poly(ethylene oxide)- b -poly(2-vinyl pyridine) (PEO-P2VP), by coupling it with the IO 3 --SO 3 2--Fe(CN) 6 2- (ISF) oscillator, and investigated its rhythmic self-assembly behavior. Furthermore, we proposed a mechanistic model to simulate the kinetics of the ISF oscillator coupling with different amounts of PEO-P2VP. Rhythmic core-shell reversal of the polymer micelles formed by PEO-P2VP was found in the ISF oscillator. The mechanistic model we proposed successfully reproduced the experimental oscillation and provided some data on the kinetics of the dual responsive self-assembly of PEO-P2VP. This line of research provided an example of realizing dissipative self-assembly of dual-responsive building blocks, which was seldom reported previously. It once again suggested that coupling with a suitable chemical oscillator is a promising strategy to have an insight into the kinetics of stimuli-responsive self-assembly. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00219797
Volume :
615
Database :
Academic Search Index
Journal :
Journal of Colloid & Interface Science
Publication Type :
Academic Journal
Accession number :
155655836
Full Text :
https://doi.org/10.1016/j.jcis.2022.01.183