Morphological Transitions of a Photoswitchable Aramid Amphiphile Nanostructure
- Authors
- Kim, Dae-Yoon; Christoff-Tempesta, Ty; Lamour, Guillaume; Zuo, Xiaobing; Ryu, Ki-Hyun; Ortony, Julia H.
- Issue Date
- 2021-04-14
- Publisher
- AMER CHEMICAL SOC
- Citation
- NANO LETTERS, v.21, no.7, pp.2912 - 2918
- 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.
- Keywords
- STILBENE; CRYSTAL; PHOTOISOMERIZATION; ISOMERIZATION; AZOBENZENE; MOLECULES; SPECTRA; TRANS; STILBENE; CRYSTAL; PHOTOISOMERIZATION; ISOMERIZATION; AZOBENZENE; MOLECULES; SPECTRA; TRANS; Small-molecule self-assembly; aramid amphiphile; photoisomerization; nanoribbon; nanotube
- ISSN
- 1530-6984
- URI
- https://pubs.kist.re.kr/handle/201004/117134
- DOI
- 10.1021/acs.nanolett.0c05048
- Appears in Collections:
- KIST Article > 2021
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