2005
DOI: 10.1039/b411380b
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A water-soluble derivative of tetrathiafulvalene exhibiting pH sensitive redox properties

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Cited by 19 publications
(7 citation statements)
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References 33 publications
(4 reference statements)
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“…The results can be assigned as the two-step one-electron oxidations, TTF + /TTF and TTF 2+ /TTF + , since the redox properties of TTF derivatives have been well characterized. Comparing with the data of 1 (0.280 and 0.556 V) measured in H 2 O-CH 3 CN (1:1 v/v) [18], a positive potential shift of the data was observed. The result is reasonable, since the redox active species is a dicarboxylate anion, which is more stable in higher polar solvent and hydrogen bonding solvent in redox view.…”
mentioning
confidence: 63%
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“…The results can be assigned as the two-step one-electron oxidations, TTF + /TTF and TTF 2+ /TTF + , since the redox properties of TTF derivatives have been well characterized. Comparing with the data of 1 (0.280 and 0.556 V) measured in H 2 O-CH 3 CN (1:1 v/v) [18], a positive potential shift of the data was observed. The result is reasonable, since the redox active species is a dicarboxylate anion, which is more stable in higher polar solvent and hydrogen bonding solvent in redox view.…”
mentioning
confidence: 63%
“…The result is reasonable, since the redox active species is a dicarboxylate anion, which is more stable in higher polar solvent and hydrogen bonding solvent in redox view. Because of the partial hydrolyzation of 1, a new peak ðE 0 ox ð1ÞÞ appears at 0.70 V in the first redox process, that is the oxidation of the protonated salt, HL À to HL [18]. In the second redox process, only one pair of peak appeared.…”
mentioning
confidence: 96%
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“…The precursor Yb(hfac) 3¨2 H 2 O (hfac´= 1,1,1,5,5,5-hexafluoroacetylacetonate anion) and the ligand Na 2 L were synthesized following previously reported methods [34,35]. All other reagents were commercially available and used without further purification.…”
Section: Synthesis General Procedures and Materialsmentioning
confidence: 99%
“…These ester moieties could also be hydrolysed into carboxylate functions acting as additional coordinating sites [60].…”
Section: Synthesismentioning
confidence: 99%