A sodium ion-sensitive tetrathiafulvalene: preparation and redox properties
- 1 January 1992
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 21,p. 1550-1552
- https://doi.org/10.1039/c39920001550
Abstract
The new tetrathiafulvalene derivative 4 has been synthesized in good yield, two crown ether moieties being annelated to the tetrathiafulvalene skeleton in the 2,3 and 6,7-positions; the redox potential of this compound has been shown to be sensitive to the presence of sodium ions.Keywords
This publication has 13 references indexed in Scilit:
- Crown-type compounds — An introductory overviewPublished by Springer Nature ,2007
- Lariat ethers: from simple sidearms to supramolecular systemsChemical Society Reviews, 1992
- Ferrocenyldimethyl-[2.2]-cryptand: solid state structure of the external hydrate and alkali and alkaline-earth-dependent electrochemical behaviourJournal of the Chemical Society, Chemical Communications, 1991
- Supramolekulare ChemiePublished by Springer Nature ,1989
- Synthesis, Reactions, and Selected Physico-Chemical Properties of 1,3-and 1,2-TetrachalcogenafulvalenesSulfur reports, 1987
- Crowned Tetrathiafulvalene DerivativesBulletin of the Chemical Society of Japan, 1985
- Superconductivity in a synthetic organic conductor (TMTSF)2PF 6Journal de Physique Lettres, 1980
- Principles and Synthetic Applications in Crown Ether ChemistrySynthesis, 1976
- Preparation of Tetrathiafulvalenes (TTF) and their Selenium Analogs -Tetraselenafulvalenes (TSeF)Synthesis, 1976
- Superconducting fluctuations and the peierls instability in an organic solidSolid State Communications, 1973