1967
DOI: 10.1016/s0040-4039(00)90819-0
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Transformations of dodecyl pyridinium bromide I. Reaction with cyanide ion

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Cited by 14 publications
(7 citation statements)
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“…Further, we were able to record in situ spectra of the following intermediate species, i.e., BQH• and BQH", employing our spectrometer. The details of these observations and chemistries involved in BQ reduction are reported elsewhere (32) reduced chemically (33,34), photochemically (35)(36)(37), or electrochemically (38)(39)(40)(41)(42). When MV is electrochemically reduced, two reversible reduction reactions are observed MV2+ + e-= MV+-…”
Section: Resultsmentioning
confidence: 99%
“…Further, we were able to record in situ spectra of the following intermediate species, i.e., BQH• and BQH", employing our spectrometer. The details of these observations and chemistries involved in BQ reduction are reported elsewhere (32) reduced chemically (33,34), photochemically (35)(36)(37), or electrochemically (38)(39)(40)(41)(42). When MV is electrochemically reduced, two reversible reduction reactions are observed MV2+ + e-= MV+-…”
Section: Resultsmentioning
confidence: 99%
“…As the viologen compound, 1,1 -didodecyl-4,4 -bipyridinium (DDV 2+ ) dibromide [31][32][33] was employed. The DDV 2+ was prepared by refluxing a dimethylformamide solution containing 4,4 -bipyridine and n-dodecylbromide (1:6 mol ratio) for 6.5 h. The product was filtered after cooling and washed with acetone.…”
Section: Materials and Electrodeposition Of Viologen Filmsmentioning
confidence: 99%
“…It has been suggested that this difference in reactivity may be due to micelle formation in the case of the dodecyl derivative, which is known to occur in the concentrations used in these studies (206). It has been suggested that this difference in reactivity may be due to micelle formation in the case of the dodecyl derivative, which is known to occur in the concentrations used in these studies (206).…”
Section: Quaternary Pyridinium Compoundsmentioning
confidence: 99%
“…Dodecylpyridinium bromide forms the viologen cation radical 111-168 directly when treated with aqueous sodium cyanide at room temperature, possibly due to micelle formation (206) …”
Section: Biomolecular Reduction Productsmentioning
confidence: 99%