Issue 17, 1971

Radical-anions and dianions of methylphenylacetylene. The role of dianions in protonation and electron-transfer processes

Abstract

Kinetic and product studies show that electron transfer to methyl(phenyl)acetylene (MPA) gives its dianions (MPA2–,2Na+) which are protonated by MPA yielding Ph[C with combining macron][double bond, length as m-dash]CHMe,Na+ and Ph[C with combining macron][double bond, length as m-dash]C[double bond, length as m-dash]CH2,Na+ as the products.

Article information

Article type
Paper

J. Chem. Soc. D, 1971, 1029-1031

Radical-anions and dianions of methylphenylacetylene. The role of dianions in protonation and electron-transfer processes

G. Levin and M. Szwarc, J. Chem. Soc. D, 1971, 1029 DOI: 10.1039/C29710001029

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