Powered by OpenAIRE graph
Found an issue? Give us feedback
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Archivio istituziona...arrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
versions View all 2 versions
addClaim

Mechanochemical activation for sustainable oxidation of benzylic alcohols

Authors: Fabio Trigatti; Daniele Zuccaccia; Walter Baratta; Eleonora Aneggi;

Mechanochemical activation for sustainable oxidation of benzylic alcohols

Abstract

This study focuses on developing a new sustainable synthesis method for oxidizing alcohols into carbonyl compounds using a mechanochemical protocol. Oxidation reactions are widely employed in the chemical industry; however, they generate large amounts of waste and score poorly on green chemistry metrics.1 As reported in the literature, mechanochemistry has proven to be a valuable tool for chemists to achieve more sustainable reactions2 and to activate catalytic processes.3 Preliminary studies in this work have shown that the use of copper-supported catalysts in combination with TEMPO can effectively oxidize p-hydroxybenzyl alcohol into its corresponding carbonyl compound. After three hours of reaction a conversion about 80% is achieved (Figure 1). The solid reagents are placed in the mixing vial and then subjected to ball milling. The green assessment4,5,6 indicates that this method presents greener parameters compared to the equivalent solution synthesis. Additionally, it is less energy and time intensive and offer better selectivity.

Country
Italy
Related Organizations
Keywords

Organometallic chemistry

  • BIP!
    Impact byBIP!
    selected citations
    These citations are derived from selected sources.
    This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    0
    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Average
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    Average
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Average
Powered by OpenAIRE graph
Found an issue? Give us feedback
selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
0
Average
Average
Average
Upload OA version
Are you the author of this publication? Upload your Open Access version to Zenodo!
It’s fast and easy, just two clicks!