4.8 Article

Self-Resetting Bistable Redox Molecular Machines for Fullerene Recognition

Journal

ORGANIC LETTERS
Volume 24, Issue 32, Pages 5879-5883

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.2c01856

Keywords

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Funding

  1. Spanish Ministry of Science, Innovation and Universities (MCIU) [PGC2018- 096880-A-I00, PGC2018-099470-B-I00]
  2. University of Valladolid (UVa)
  3. Junta de Castilla y Leon [EDU/574/2018]

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This article discusses the use of mimicking natural mechanisms to address control and output modulation of molecular machines. The reversible thiol/disulfide motifs in chemical systems are utilized with nonplanar corannulene moieties capable of recognizing fullerenes. Two redox-based machines have been devised: an ON/OFF switch activated by dimerization and a self-resetting host with an automated backward process that substantially modulates its affinity.
Addressing control over molecular machines resulting in variable output modulation by mimicking nature mechanisms is a current hot topic. The exploitation of reversibility in thiol/disulfide motifs in chemical systems flanked by nonplanar corannulene moieties capable to recognize fullerenes is presented herein. Two redox-based machines have been conceived for this purpose: an ON/OFF switch that activates its binding properties upon dimerization and a self-resetting (i.e., with an automated backward process) host that substantially modulates its affinity.

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