Direct Syntheses of Tetrathiafulvalene and Bis(ethylenedithio)tetrathiafulvalene By a Non-Coupling Route from 1,4,5,8-Tetrathianaphthalene
Ronald L. Meline, Ronald L. Elsenbaumer
Abstract
Ronald L. Meline, Ronald L. Elsenbaumer
Abstract
All articles of this category 1,3,5,8-Tetrathianaphthalene ( 2 , TTN; 1,4,5,8-tetrathiatetralin) has been synthesized in one step from 4,5-bis(benzoylthio)-1,3-dithiole-2-thione (1) and cis -dichloroethylene in high yield. TTN (2) is readily converted into tetrathiafulvalene ( 2 , TTF) upon tetralithiation or bis(ethylenedithio)tetrathiafulvalene ( 4 , BEDT-TTF) upon tetralithiation, sulfur insertion into the carbon-lithium bond pairs and subsequent capping of the reactive intermediate with 1,2-dibromoethane. The rearrangement of TTN allows for a facile synthesis of TTF and a novel non-coupling route to BEDT-TTF. superconductivity - tetrathianaphthalene - tetrathiafulvalene - bis(ehtylenedithio)tetrathiafulvalene - 13 C-NMR
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All articles of this category 1,3,5,8-Tetrathianaphthalene ( 2 , TTN; 1,4,5,8-tetrathiatetralin) has been synthesized in one step from 4,5-bis(benzoylthio)-1,3-dithiole-2-thione (1) and cis -dichloroethylene in high yield. TTN (2) is readily converted into tetrathiafulvalene ( 2 , TTF) upon tetralithiation or bis(ethylenedithio)tetrathiafulvalene ( 4 , BEDT-TTF) upon tetralithiation, sulfur insertion into the carbon-lithium bond pairs and subsequent capping of the reactive intermediate with 1,2-dibromoethane. The rearrangement of TTN allows for a facile synthesis of TTF and a novel non-coupling route to BEDT-TTF. superconductivity - tetrathianaphthalene - tetrathiafulvalene - bis(ehtylenedithio)tetrathiafulvalene - 13 C-NMR
Key concepts: Tetrathiafulvalene, Chemistry, Yield (engineering), Lithium (medication), Sulfur, Stereochemistry, Medicinal chemistry, Molecule