journal article·2017-11

Stimulated Transitions of Directed Nonequilibrium Self‐Assemblies

Alexander A. Steinschulte, Andrea Scotti, Khosrow Rahimi, Oleksii Nevskyi, Alex Oppermann, Sabine Schneider, Steffen Bochenek, Marie F. Schulte, Karen Geisel, Felicitas Jansen, Andre Jung, Sabrina Mallmann, Roland Winter, Walter Richtering, Dominik Wöll, Ralf Schweins, Nicholas J. Warren, Felix A. Plamper

Advanced Materials· Volume 29· Issue 43
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Abstract

Abstract Near‐equilibrium stimulus‐responsive polymers have been used extensively to introduce morphological variations in dependence of adaptable conditions. Far‐less‐well studied are triggered transformations at constant conditions. These require the involvement of metastable states, which are either able to approach the equilibrium state after deviation from metastability or can be frozen on returning from nonequilibrium to equilibrium. Such functional nonequilibrium macromolecular systems hold great promise for on‐demand transformations, which result in substantial changes in their material properties, as seen for triggered gelations. Herein, a diblock copolymer system consisting of a hydrophilic block and a block that is responsive to both pressure and temperature, is introduced. This species demonstrates various micellar transformations upon leaving equilibrium/nonequilibrium states, which are triggered by a temperature deflection or a temporary application of hydrostatic pressure.
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Research context

OpenAlex topics: Advanced Polymer Synthesis and Characterization · Supramolecular Self-Assembly in Materials · Polymer Surface Interaction Studies

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Institute of Physical Chemistry RWTH Aachen University Landoltweg 2 D‐52056 Aachen Germany

DWI Leibniz Institute for Interactive Materials and Center for Chemical Polymer Technology (CPT) Forckenbeckstr. 50 D‐52074 Aachen Germany

Department of Chemistry and Chemical Biology Physical Chemistry I TU Dortmund University Otto‐Hahn Str. 6 D‐44227 Dortmund Germany

Institut Laue‐Langevin ILL DS/LSS 71 Avenue des Martyrs F‐38000 Grenoble France

School of Chemical and Process Engineering University of Leeds Leeds LS2 9JT UK

Funding

Deutsche Forschungsgemeinschaft

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