Issue 0, 1973

Steric inhibition of resonance studied by molecular photoelectron spectroscopy. Part 3.—Anilines, phenols and related compounds

Abstract

Photoelectron spectroscopic data for amino- and oxy-benzenes are discussed in terms of a simple p-π interaction scheme. Steric hindrance is shown only to be important in ortho substituted NN-dialkylanilines and in 2,6-dimethylanisole. In the nitrogen series there is indication that the N atom is not planar.

Article information

Article type
Paper

J. Chem. Soc., Faraday Trans. 2, 1973,69, 521-531

Steric inhibition of resonance studied by molecular photoelectron spectroscopy. Part 3.—Anilines, phenols and related compounds

J. P. Maier and D. W. Turner, J. Chem. Soc., Faraday Trans. 2, 1973, 69, 521 DOI: 10.1039/F29736900521

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