| Literature DB >> 33733794 |
Dae-Yoon Kim1,2, Ty Christoff-Tempesta1, Guillaume Lamour3, Xiaobing Zuo4, Ki-Hyun Ryu2, Julia H Ortony1.
Abstract
Self-assembly of small amphiphilic molecules in water can lead to nanostructures of varying geometries with pristine internal molecular organization. Here we introduce a photoswitchable aramid amphiphile (AA), designed to exhibit extensive hydrogen bonding and robust mechanical properties upon self-assembly, while containing a vinylnitrile group for photoinduced cis-trans isomerization. We demonstrate spontaneous self-assembly of the vinylnitrile-containing AA in water to form nanoribbons. Upon UV irradiation, trans-to-cis isomerizations occur concomitantly with a morphological transition from nanoribbons to nanotubes. The nanotube structure persists in water for over six months, stabilized by strong and collective intermolecular interactions. We demonstrate that the nanoribbon-to-nanotube transition is reversible upon heating and that switching between states can be achieved repeatedly. Finally, we use electron microscopy to capture the transition and propose mechanisms for nanoribbon-to-nanotube rearrangement and vice versa. The stability and switchability of photoresponsive AA nanostructures make them viable for a range of future applications.Entities:
Keywords: Small-molecule self-assembly; aramid amphiphile; nanoribbon; nanotube; photoisomerization
Year: 2021 PMID: 33733794 DOI: 10.1021/acs.nanolett.0c05048
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189