| Literature DB >> 25393204 |
Thomas Heuser1, Ann-Kathrin Steppert1, Catalina Molano Lopez1, Baolei Zhu1, Andreas Walther1.
Abstract
Nature regulates complex structures in space and time via feedback loops, kinetically controlled transformations, and under energy dissipation to allow non-equilibrium processes. Although man-made static self-assemblies realize excellent control over hierarchical structures via molecular programming, managing their temporal destiny by self-regulation is a largely unsolved challenge. Herein, we introduce a generic concept to control the time domain by programming the lifetimes of switchable self-assemblies in closed systems. We conceive dormant deactivators that, in combination with fast promoters, enable a unique kinetic balance to establish an autonomously self-regulating, transient pH-state, whose duration can be programmed over orders of magnitude-from minutes to days. Coupling this non-equilibrium state to pH-switchable self-assemblies allows predicting their assembly/disassembly fate in time, similar to a precise self-destruction mechanism. We demonstrate a platform approach by programming self-assembly lifetimes of block copolymers, nanoparticles, and peptides, enabling dynamic materials with a self-regulation functionality.Entities:
Keywords: Dynamic Properties; Non-Equilibrium Self-Assembly; Programmable Materials; Self-Regulation; Switchable Materials; Time Domain
Year: 2014 PMID: 25393204 DOI: 10.1021/nl5039506
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189