Self‐Assembly of Photoresponsive Molecular Amphiphiles in Aqueous Media

Amphiphilic molecules, comprising hydrophobic and hydrophilic moieties and the intrinsic propensity to self‐assemble in aqueous environment, sustain a fascinating spectrum of structures and functions ranging from biological membranes to ordinary soap. Facing the challenge to design responsive, adapt...

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Veröffentlicht in:Angewandte Chemie 2021-05, Vol.133 (21), p.11708-11731
Hauptverfasser: Chen, Shaoyu, Costil, Romain, Leung, Franco King‐Chi, Feringa, Ben L.
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Sprache:eng
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Zusammenfassung:Amphiphilic molecules, comprising hydrophobic and hydrophilic moieties and the intrinsic propensity to self‐assemble in aqueous environment, sustain a fascinating spectrum of structures and functions ranging from biological membranes to ordinary soap. Facing the challenge to design responsive, adaptive, and out‐of‐equilibrium systems in water, the incorporation of photoresponsive motifs in amphiphilic molecular structures offers ample opportunity to design supramolecular systems that enables functional responses in water in a non‐invasive way using light. Here, we discuss the design of photoresponsive molecular amphiphiles, their self‐assembled structures in aqueous media and at air–water interfaces, and various approaches to arrive at adaptive and dynamic functions in isotropic and anisotropic systems, including motion at the air–water interface, foam formation, reversible nanoscale assembly, and artificial muscle function. Controlling the delicate interplay of structural design, self‐assembling conditions and external stimuli, these responsive amphiphiles open several avenues towards application such as soft adaptive materials, controlled delivery or soft actuators, bridging a gap between artificial and natural dynamic systems. Dynamic self‐assembly of photoresponsive molecular amphiphiles at Gibbs monolayers, i.e., air–water interfaces, and in solutions, ranging from isotropic assembly transformations to anisotropic three‐dimensional structures, provides the amplification of molecular motion to macroscopic functions.
ISSN:0044-8249
1521-3757
DOI:10.1002/ange.202007693