A DTA study of phenols |
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Authors: | N. G. Buckman J. O. Hill R. J. Magee |
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Affiliation: | 1. Materials Chemistry Section, Herman Research Laboratory, State Electricity Commission, 3121, Richmond, Victoria, Australia 2. Department of Chemistry, La Trobe University, 3083, Bundoora, Victoria, Australia
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Abstract: | A comprehensive DTA study is reported of 17 halophenols and of the corresponding p-nitrobenzoylchloride 3,5-dinitrobenzoylchloride and p-phenylazobenzoylchloride derivatives, prepared “in-situ”by heating intimate mixtures of phenol and acid chloride in the DTA system. The thermal analysis data, in particular, the derivative formation temperatures, are interpreted in terms of the inductive, mesomeric and steric effects associated with the ring substituents of the phenol and acid chloride and the extent of inter- and intramolecular hydrogen-bonding existing in these systems. The DTA data collectively provide a reference base for the identification and characterization of halophenols via thermal analysis. |
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