Issue 5, 1991

Monofunctionalized tridecachlorodiphenyl (2-pyridyl)methyl radicals. Synthesis and spectral analysis

Abstract

Highly chlorinated diphenyl(2-pyridyl)methyl radicals and their α-H precursors with a carboxy, chlorocarbonyl, or allyloxycarbonyl substituent in the 4-position of one phenyl ring have been synthesized. All of them are stable red solids, completely dissociated, (magnetic susceptibility), decomposing when melting (200–240 °C). Their ESR, UV–VIS and IR spectra are given.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1991, 1101-1105

Monofunctionalized tridecachlorodiphenyl (2-pyridyl)methyl radicals. Synthesis and spectral analysis

L. Julia, J. Riera and R. Teixidó, J. Chem. Soc., Perkin Trans. 1, 1991, 1101 DOI: 10.1039/P19910001101

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