Issue 0, 1971

Tautomeric pyridines. Part XII. The stabilisation of hydroxy-forms by intramolecular hydrogen-bonding

Abstract

A series of 10-hydroxy-1,7-phenanthrolines are shown to prefer the hydroxy- to the pyridone-form for both polar and nonpolar media. This tendency results both from stabilisation of the hydroxy-form by intramolecular hydrogen-bonding, similar examples of which are discussed, and from destabilisation of the pyridone form by electron repulsion terms.

Article information

Article type
Paper

J. Chem. Soc. B, 1971, 2339-2344

Tautomeric pyridines. Part XII. The stabilisation of hydroxy-forms by intramolecular hydrogen-bonding

G. P. Bean, M. J. Cook, T. M. Dand, A. R. Katritzky and J. R. Lea, J. Chem. Soc. B, 1971, 2339 DOI: 10.1039/J29710002339

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