1972
DOI: 10.1016/s0022-328x(00)80445-3
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Exchange of organomercury compounds with mercury metal

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Cited by 25 publications
(13 citation statements)
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“…Charging curves of Et 2 Hg unexpectedly revealed a faradaic delay in addition to the adsorption ± desorption delay at ca. 71 V. 109,110 The faradaic delay potential coincided with E 2 1a2 of EtHgBr and the parameters of the corresponding Tafel plots also turned out to be close. 110 Moreover, it is known 1, 67 that many Alk 2 Hg compounds either reduced by the two-electron mechanism at very high cathodic potentials or were altogether polarographically inactive.…”
Section: Hoch2ch2hgmentioning
confidence: 70%
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“…Charging curves of Et 2 Hg unexpectedly revealed a faradaic delay in addition to the adsorption ± desorption delay at ca. 71 V. 109,110 The faradaic delay potential coincided with E 2 1a2 of EtHgBr and the parameters of the corresponding Tafel plots also turned out to be close. 110 Moreover, it is known 1, 67 that many Alk 2 Hg compounds either reduced by the two-electron mechanism at very high cathodic potentials or were altogether polarographically inactive.…”
Section: Hoch2ch2hgmentioning
confidence: 70%
“…71 V. 109,110 The faradaic delay potential coincided with E 2 1a2 of EtHgBr and the parameters of the corresponding Tafel plots also turned out to be close. 110 Moreover, it is known 1, 67 that many Alk 2 Hg compounds either reduced by the two-electron mechanism at very high cathodic potentials or were altogether polarographically inactive. Thus diethylmercury could not be reduced on a Hg electrode up to 72.8 V. 127 Hence, the following two conclusions can be inferred: Ð upon adsorption on mercury, Et 2 Hg was transformed into an electroactive substance [EtHg] analogous to the product of the first step of the EtHgBr electroreduction;…”
Section: Hoch2ch2hgmentioning
confidence: 70%
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