Issue 9, 1969

A tripositive organic ion: anodic pyridination of tris-p-methoxyphenylethylene

Abstract

Anodic oxidation of tris-(p-methoxyphenyl)-ethylene in the presence of pyridine results in the intermediate formation of the monopyridinium salt of a trication, which undergoes quasi-reversible reduction under cyclic voltammetry conditions.

Article information

Article type
Paper

J. Chem. Soc. D, 1969, 451-452

A tripositive organic ion: anodic pyridination of tris-p-methoxyphenylethylene

V. D. Parker and L. Eberson, J. Chem. Soc. D, 1969, 451 DOI: 10.1039/C29690000451

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