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Is Micellar Catalysis Green Chemistry?

Many years ago, twelve principles were defined for carrying out chemical reactions and processes from a green chemistry perspective. It is everyone’s endeavor to take these points into account as far as possible when developing new processes or improving existing ones. Especially in the field of org...

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Autores principales: Fabris, Fabrizio, Illner, Markus, Repke, Jens-Uwe, Scarso, Alessandro, Schwarze, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10301937/
https://www.ncbi.nlm.nih.gov/pubmed/37375364
http://dx.doi.org/10.3390/molecules28124809
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author Fabris, Fabrizio
Illner, Markus
Repke, Jens-Uwe
Scarso, Alessandro
Schwarze, Michael
author_facet Fabris, Fabrizio
Illner, Markus
Repke, Jens-Uwe
Scarso, Alessandro
Schwarze, Michael
author_sort Fabris, Fabrizio
collection PubMed
description Many years ago, twelve principles were defined for carrying out chemical reactions and processes from a green chemistry perspective. It is everyone’s endeavor to take these points into account as far as possible when developing new processes or improving existing ones. Especially in the field of organic synthesis, a new area of research has thus been established: micellar catalysis. This review article addresses the question of whether micellar catalysis is green chemistry by applying the twelve principles to micellar reaction media. The review shows that many reactions can be transferred from an organic solvent to a micellar medium, but that the surfactant also has a crucial role as a solubilizer. Thus, the reactions can be carried out in a much more environmentally friendly manner and with less risk. Moreover, surfactants are being reformulated in their design, synthesis, and degradation to add extra advantages to micellar catalysis to match all the twelve principles of green chemistry.
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spelling pubmed-103019372023-06-29 Is Micellar Catalysis Green Chemistry? Fabris, Fabrizio Illner, Markus Repke, Jens-Uwe Scarso, Alessandro Schwarze, Michael Molecules Review Many years ago, twelve principles were defined for carrying out chemical reactions and processes from a green chemistry perspective. It is everyone’s endeavor to take these points into account as far as possible when developing new processes or improving existing ones. Especially in the field of organic synthesis, a new area of research has thus been established: micellar catalysis. This review article addresses the question of whether micellar catalysis is green chemistry by applying the twelve principles to micellar reaction media. The review shows that many reactions can be transferred from an organic solvent to a micellar medium, but that the surfactant also has a crucial role as a solubilizer. Thus, the reactions can be carried out in a much more environmentally friendly manner and with less risk. Moreover, surfactants are being reformulated in their design, synthesis, and degradation to add extra advantages to micellar catalysis to match all the twelve principles of green chemistry. MDPI 2023-06-16 /pmc/articles/PMC10301937/ /pubmed/37375364 http://dx.doi.org/10.3390/molecules28124809 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Fabris, Fabrizio
Illner, Markus
Repke, Jens-Uwe
Scarso, Alessandro
Schwarze, Michael
Is Micellar Catalysis Green Chemistry?
title Is Micellar Catalysis Green Chemistry?
title_full Is Micellar Catalysis Green Chemistry?
title_fullStr Is Micellar Catalysis Green Chemistry?
title_full_unstemmed Is Micellar Catalysis Green Chemistry?
title_short Is Micellar Catalysis Green Chemistry?
title_sort is micellar catalysis green chemistry?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10301937/
https://www.ncbi.nlm.nih.gov/pubmed/37375364
http://dx.doi.org/10.3390/molecules28124809
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