2012
DOI: 10.1002/adma.201103522
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Solution‐Processable Septithiophene Monolayer Transistor

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Cited by 56 publications
(78 citation statements)
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References 34 publications
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“…In our previous report, septithiophene-TTF 3 exhibited a complex series of redox processes dispersed across a wide potential range that was difficult to explain and interpret with a high degree of 40 confidence. This was in contrast to the corresponding half unit 18 that revealed a relatively discernible redox profile, with three sequential oxidation processes.…”
Section: Electrochemistrymentioning
confidence: 95%
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“…In our previous report, septithiophene-TTF 3 exhibited a complex series of redox processes dispersed across a wide potential range that was difficult to explain and interpret with a high degree of 40 confidence. This was in contrast to the corresponding half unit 18 that revealed a relatively discernible redox profile, with three sequential oxidation processes.…”
Section: Electrochemistrymentioning
confidence: 95%
“…0.6mT line width without any hyperfine splitting, as would be expected if delocalisation over the thiophene units was to take place. [28][29][30][31] The EPR spectra of the radical cation of TTF consist of five lines, originating from coupling with four 40 equivalent protons. 32 However, here the TTF unit is bereft of hydrogen, which would explain the absence of hyperfine features.…”
Section: Spectroelectrochemistrymentioning
confidence: 99%
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“…14,15 Among these methods, SAM formation is the most reliable and convenient way to fabricate uniform and densely packed monolayer. By forming a covalent chemical bond between the molecule and substrate, a monolayer can be formed without any vacuum/heating or tedious operation.…”
Section: Introductionmentioning
confidence: 99%