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2008
DOI: 10.1016/j.colsurfa.2007.04.181
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An electrochemical study on charge-transfer phenomenon between 7,7,8,8-tetracyanoquinodimethane and a self-assembled monolayer containing tetrathiafulvalene moiety using an indium-tin oxide electrode

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Cited by 2 publications
(8 citation statements)
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“…8 It was confirmed and characterized by reflection-absorption FT-IR spectrum (Fig. 1), in which the normal alkyl chain peaks were observed at 2852 cm -1 for νsym(CH2) and 2920 cm -1 for νantisym(CH2).…”
Section: Resultsmentioning
confidence: 59%
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“…8 It was confirmed and characterized by reflection-absorption FT-IR spectrum (Fig. 1), in which the normal alkyl chain peaks were observed at 2852 cm -1 for νsym(CH2) and 2920 cm -1 for νantisym(CH2).…”
Section: Resultsmentioning
confidence: 59%
“…
Tetrathiafulvalene (TTF: C6H4S4) is a well-known two-electron donor molecule that is electrochemically active, showing two reversible redox cycles at E1/2 1 = 0.33 V and E1/2 2 = 0.71 V (vs SCE).1 It reacts with 7,7,8, to form an electrically conductive TTF-TCNQ chargetransfer (CT) complex with metallic conductivity at room temperature.2 Thereafter, many kinds of TTF-TCNQ-family CT complexes composed of, for example, ethylenedithio-tetrathiafulvalene (EDT-TTF) and 2, 3,5,7,8,, have followed. 3 In the early stage, the CT complexes in the form of a single crystal were investigated with respect to their bulk properties such as crystal structure, electrical conductivity, and optical properties.
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confidence: 99%
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