Ion‐radical mechanism of the polymerization of 2,6‐dimethylphenol by oxidative coupling catalysed by CuCl<sub>2</sub>‐amine complex

書誌事項

公開日
1975-01
権利情報
  • http://onlinelibrary.wiley.com/termsAndConditions#vor
DOI
  • 10.1002/macp.1975.021760111
公開者
Wiley

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説明

<jats:title>Abstract</jats:title><jats:p>The preparation of poly[oxy‐(2,6‐dimethyl)‐1,4‐phenylene] (<jats:bold>2</jats:bold>) via polymerization of 2,6‐dimethylphenol (<jats:bold>1</jats:bold>) by oxidative coupling with CuCl<jats:sub>2</jats:sub>‐amine complexes is described. The reaction mechanism was studied by means of ESR, NMR spectroscopy, and conductivity measurements. It was established that the CC coupling products (dipheno‐quinones) are formed by recombination of phenoxyl radicals and that the very high selectivity of the CuCl<jats:sub>2</jats:sub>‐amine complex catalysts in the formation of <jats:bold>2</jats:bold> (CO coupling) is due to the cationic mechanism based on the consecutive reaction of the phenoxyl radicals with Cu(II) complexes. This consecutive reaction of the phenoxyl radicals with Cu(II) complexes is responsible for the non‐measurable level of polymeric radicals <jats:bold>5</jats:bold> by ESR, previously reported.</jats:p>

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