A phenol-fused tetrathiafulvalene: modulation of hydrogen-bond patterns and electrical conductivity in the charge-transfer salt. (26th January 2018)

• Record Type: Journal Article
• Authors: Ueda, Akira; Mori, Hatsumi
• Is Part Of: Materials chemistry frontiers. Volume 2:Number 3(2018)
• Page Start: 566
• Page End: 572
• Publication Date: 2018-01-26
• Subjects: Materials science -- Periodicals; Chemistry -- Periodicals; 540
• DOI: 10.1039/c7qm00574a
• Languages: English
• ISSNs: 2052-1529

Abstract

Abstract : Elimination of one hydroxy group from a tetrathiafulvalene derivative changed hydrogen-bond patterns in the charge-transfer salt, leading to improved conductivity. Abstract : A tetrathiafulvalene (TTF) derivative fused with a phenol moiety, PhOH-EDT-TTF, was designed and synthesized as a new electron-donor molecule with hydrogen-bonding (H-bonding) abilities. Electrochemical oxidation of this donor molecule in the presence of Bu4 NClO4 gave a charge-transfer salt, β-(PhOH-EDT-TTF)2 ClO4, that containsPhOH-EDT-TTF +0.5 and ClO4 − in a 2 : 1 ratio. In this salt, the donor and anion molecules are connected with three-centered H-bonds through the phenol hydroxy group, which is in contrast to the linear H-bonds observed in an analogue salt based on the catechol-fused TTF. This variation in the donor-anion H-bonds modulated the arrangement of the donor molecules in the conducting layer, leading to better conducting properties than those of the analogue salt.