Syntheses, Structure and Conducting Properties of Halogenated Ethylenedioxytetrathiafulvalenes
摘要:
4,5-Diiodo-, 4,5-dibromo-, and 4,5-dichloro-4',5'-ethylenedioxytetra-thiafulvalenes (EDO-TTFI2, EDO-TTFBr2, and EDO-TTFCl2) were synthesized in moderate to good yields by the two routes. The first route contains the reaction of EDO-TTF with LDA, followed by quenching with halogenated reagents, and the second route consists of the P(OR)(3)-mediated cross-coupling of 4,5-dihalogenated 1,3-dithiole-2-ones with 4,5-ethylenedioxy-1,3-dithiole-2-thione. The structures of EDO-TTFI2 and EDO-TTFCl2 were determined by X-Ray analysis. The radical-cation salts derived from EDO-TTFI2, EDO-TTFBr2, and EDO-TTFCl2 show high conductivities, although these compounds contain electron-withdrawing halogens as the substituent.
作者:Takehiko Mori、Hiroo Inokuchi、Aravinda M. Kini、Jack M. Williams
DOI:10.1246/cl.1990.1279
日期:1990.8
Seven new electron donors, 4,5-ethylenedioxytetrathiafulvalenes where 4′,5′-substituents are trimethylenedithio, ethylenedithio, methylenedithio, 2-oxatrimethylenedithio, methylthio, hydrogen and methyl carboxylate, are prepared, and their electrochemical properties are investigated.
An organic superconductor, (TEA)(HEDO-TTF-dc)<sub>2</sub>·2(H<sub>2</sub>C<sub>2</sub>O<sub>4</sub>), coupled with strong hydrogen-bonding interactions
organic superconductor (TEA)(HEDO-TTF-dc)2·2(H2C2O4) (H2EDO-TTF-dc = ethylenedioxy-tetrathiafulvalene dicarboxylic acids) with an onset TC of 4.0 K, was successfully obtained using oxalic acid and HEDO-TTF-dc anion donor. The crystal structure analysis indicated that strong π–π overlaps and very strong intra- and inter-molecular hydrogen-bonding interactions exist between the HEDO-TTF-dc anion donors