Donor-Acceptor-Komplexe des 1.3-II.3 '-Tetrathiafulvalene 1 und des Selen-Analogen mit Tetracyanochinodimethan zeigen im Festzustand ungewijhnlich hohe anisotrope elektronische Leitflihigkeit ("Organiache Hetalle") 1) , das sugehijrige Tetrathiafulvaleniumchlorid Ralbleiter-Eigenschaften 213) . Vert
Tetrathiafulvalene; Naphthochinon-(1,2)-[(1,3)-dithiol-(2)-methid]-Tetracyano-chinodimethan-Komplexe
✍ Scribed by Egon Fanghänel; Wolfgang John; Helmut Fricke; Gottfried Kempe
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 2010
- Weight
- 276 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0044-2402
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
2-BUTYNE-1,4-DIYLIDENE-2,2'BIS (13DlTHIOLE) : ACETYLENIC ANALOGS OF TETRATHIAFULVALENE Abddlah KHANOUS, Alain GORGUES\* and Fanand TEXER. Laboratoi~ de Synth&se Organique et d'Electrochimie. ~niversit&d'hgers, 2, boulevard Lavoisier, 49045 Angers ,Prancc. w : The title compounds can be pmpared throu
The cycloaddition of hex-3-yn-2,5-dione onto a rc-CS2 Iron complex 3 and on 3-thioxo-1.2dithioles affords diietylated intermediates which can be readily converted into di or tetraacetylated derivatives of the 1,3-dithiole (5,6) and tetrathiafulvalene (2.8) series, some represemative electrochemical
Reacting 2-lithio-1,3-dithioles with 1,3-dithiolium salts results in formation of both symmetrical and unsymmetrical tetrathiafulvalenes. The symmetrical tetra-thiafulvalenes are probably formed via a carbene intermediate which is generated by loss of an hydride from the 2-lithio-1,3dithioles.