Skip to main navigation Skip to search Skip to main content

Azobenzene Molecular Machine: Light-Induced Wringing Gel Fabricated from Asymmetric Macrogelator

  • Yu Jin Choi
  • , Ji Tae Kim
  • , Won Jin Yoon
  • , Dong Gue Kang
  • , Minwook Park
  • , Dae Yoon Kim
  • , Myong Hoon Lee
  • , Suk Kyun Ahn*
  • , Kwang Un Jeong
  • *Corresponding author for this work
  • Jeonbuk National University
  • Pusan National University

Research output: Contribution to journalJournal articlepeer-review

Abstract

To develop light-triggered wringing gels, an asymmetric macrogelator (1AZ3BP) was newly synthesized by the chemically bridging a photoisomerizable azobenzene (1AZ) molecular machine and a biphenyl-based (3BP) dendron with a 1,4-phenylenediformamide connector. 1AZ3BP was self-assembled into a layered superstructure in the bulk state, but 1AZ3BP formed a three-dimensional (3D) network organogel in solution. Upon irradiating UV light onto the 3D network organogel, the solvent of the organogel was squeezed and the 3D network was converted to the layered morphology. It was realized that the metastable 3D network organogels were fabricated mainly due to the nanophase separation in solution. UV isomerization of 1AZ3BP provided sufficient molecular mobility to form strong hydrogen bonds for the construction of the stable layered superstructure. The light-triggered wringing gels can be smartly applied in remote-controlled generators, liquid storages, and sensors.

Original languageEnglish
Pages (from-to)576-581
Number of pages6
JournalACS Macro Letters
Volume7
Issue number5
DOIs
StatePublished - 2018.05.15

Quacquarelli Symonds(QS) Subject Topics

  • Materials Science
  • Engineering - Petroleum
  • Chemistry

Fingerprint

Dive into the research topics of 'Azobenzene Molecular Machine: Light-Induced Wringing Gel Fabricated from Asymmetric Macrogelator'. Together they form a unique fingerprint.

Cite this