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Electrodes functionalized with the 2,2,6,6-tetramethylpiperidinyloxy radical for the waste-free oxidation of alcohols

  • Istituto Per Lo Studio Dei Materiali Nanostrutturati, Rome

Research output: Contribution to journalArticlepeer-review

48 Scopus citations

Abstract

Electrodes functionalised with the organocatalyst 2,2,6,6-tetramethylpiperidinyloxy (TEMPO) moiety hold great potential for the development of waste-free industrial synthesis of valuable carbonyl compounds using electrons and alcohols as the only reactants. Since the inception of the first active electrode in 1988, a number of different electrodes have been developed to the recent fastest TEMPO-mediated alcohol oxidation process ever reported. In addition to good activity and broad applicability to different substrates, the electrode stability is the crucial factor that will guide the adoption of this eminently clean technology by the fine chemical and pharmaceutical industry. Selective oxidation with electricity only: Electrodes functionalized with the organocatalyst 2,2,6,6-tetramethylpiperidinyloxy (TEMPO) hold great potential for the development of the entirely waste-free industrial synthesis of valuable carbonyl compounds in the fine chemical and pharmaceutical industries.

Original languageBritish English
Pages (from-to)552-558
Number of pages7
JournalChemCatChem
Volume7
Issue number4
DOIs
StatePublished - Feb 2015

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 12 - Responsible Consumption and Production
    SDG 12 Responsible Consumption and Production

Keywords

  • alcohols
  • electrochemistry
  • organocatalysis
  • oxidation
  • waste prevention

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