The effects of adsorption conformation of intermediates on the kinetic parameters of an electrode process mechanism of the electroreduction of chloropyridines on the DME

Kashti, S.; Kirowa‐Eisner, E.

doi:10.1016/s0022-0728(79)80483-0

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Halogenated Heterocyclic Compounds1

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Cited by 13 publications

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“…Accordingly, at mercury in aqueous media, monohalogenated pyridines, in either their unprotonated or protonated forms, undergo a two-electron cleavage of the carbon-halogen bond, followed by protonation to yield pyridine [106]. Redox catalysis has been used to probe the reduction of 2-bromo-, 3-bromo-, 2-chloro-, and 3-chloropyridine at mercury [58].…”

Section: Halogenated Heterocyclic Compoundsmentioning

confidence: 99%

Oxidation and Reduction of Halogen‐containing Compounds

Peters

2004

Encyclopedia of Electrochemistry

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The sections in this article are Introduction Anodic Processes Halogenated Alkanes Alicyclic Halides Aryl Halides Cathodic Processes Halogenated Alkanes Halogenated Alkenes and Alkynes Benzyl Halides Alicyclic Halides Aryl Halides Acyl and Phenacyl Halides Aliphatic α‐Halocarbonyl Compounds Halogenated Heterocyclic Compounds Catalytic Reduction of Carbon–Halogen Bonds

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Section: Halogenated Heterocyclic Compoundsmentioning

confidence: 99%