Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Tetrathiafulvalene crowns: redox-switchable ligands.

F Le Derf1, M Mazari, N Mercier

  • 1Laboratoire d'Ingénierie Moléculaire et Matériaux Organiques, UMR CNRS 6501, Université d'Angers, France.

Chemistry (Weinheim an Der Bergstrasse, Germany)
|March 29, 2001
PubMed
Summary

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Processus organisationnels et pratiques cliniques pour la gestion de la douleur chronique en soins primaires : une offre de service découlant du plan d'action en douleur chronique 2021-2026 ministériel du Québec, Canada.

Canadian journal of pain = Revue canadienne de la douleur·2026
Same author

Black Hole Spectroscopy and Tests of General Relativity with GW250114.

Physical review letters·2026
Same author

GW250114: Testing Hawking's Area Law and the Kerr Nature of Black Holes.

Physical review letters·2025
Same author

A new case of sodium-dependent multivitamin transporter defect occurring as a life-threatening condition responsive to early vitamin supplementation and literature review.

Molecular genetics & genomic medicine·2024
Same author

Successful removal of fluoride from aqueous environment using Al(OH)<sub>3</sub>@AC: column studies and breakthrough curve modeling.

RSC advances·2024
Same author

Frequency-Dependent Squeezed Vacuum Source for the Advanced Virgo Gravitational-Wave Detector.

Physical review letters·2023

New redox-responsive ligands combine tetrathiafulvalene (TTF) with polyethers. These switchable ligands show high metal cation recognition, with structures confirmed by X-ray crystallography.

Area of Science:

  • Supramolecular Chemistry
  • Organic Synthesis
  • Coordination Chemistry

Background:

  • Redox-responsive ligands offer tunable properties for molecular recognition.
  • Tetrathiafulvalene (TTF) is a versatile electroactive unit for developing functional materials.
  • Crown ethers are known for their ability to complex metal cations.

Purpose of the Study:

  • To synthesize novel redox-responsive ligands by associating the tetrathiafulvalene core with polyether subunits.
  • To investigate the metal cation recognition capabilities of these ligands as a function of their cavity size.
  • To characterize the structural and electronic properties of the synthesized ligands and their metal complexes.

Main Methods:

  • Ligand synthesis and purification.

Related Experiment Videos

  • X-ray crystallography for structural determination of free ligands and metal complexes.
  • Spectroscopic techniques including LSIMS, 1H NMR, and UV/Vis spectroscopy.
  • Electrochemical analysis using cyclic voltammetry.
  • Main Results:

    • Successful synthesis of redox-responsive ligands featuring TTF and polyether chains.
    • X-ray structures confirmed the planarity of the TTF pi system and suitable coordinating atoms for switchable ligation.
    • Demonstrated high coordination ability for various metal cations (Pb2+, Sr2+, Ba2+) with cavity size-dependent recognition.
    • Cyclic voltammetry confirmed switchable ligating properties.
    • X-ray structures of metal complexes revealed original packing modes with channel-like arrangements.

    Conclusions:

    • The synthesized TTF-polyether ligands exhibit excellent metal cation binding properties.
    • These ligands represent a new class of switchable receptors with potential applications in sensing and separation.
    • The structural diversity of the metal complexes highlights the versatility of these novel ligand systems.