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Experimental and Theoretical Study on the Homodimerization Mechanism of 3-Acetylcoumarin
In the present study, the reaction conditions for homodimerization process of 3-acetylcoumarin were achieved under sonication using combination of zinc and metallic salt (ZnCl(2) or Zn(OAc)(2)). Appropriate frequency and sound amplitude have been identified as significant variables for the initiatio...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9655359/ https://www.ncbi.nlm.nih.gov/pubmed/36364063 http://dx.doi.org/10.3390/molecules27217228 |
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author | Simeonova, Kristina B. Koleva, Ana I. Zlatanova, Anna-Mariya R. Petkova-Yankova, Nevena I. Aleksandrov, Hristiyan A. Petkov, Petko St. Nikolova, Rositca D. |
author_facet | Simeonova, Kristina B. Koleva, Ana I. Zlatanova, Anna-Mariya R. Petkova-Yankova, Nevena I. Aleksandrov, Hristiyan A. Petkov, Petko St. Nikolova, Rositca D. |
author_sort | Simeonova, Kristina B. |
collection | PubMed |
description | In the present study, the reaction conditions for homodimerization process of 3-acetylcoumarin were achieved under sonication using combination of zinc and metallic salt (ZnCl(2) or Zn(OAc)(2)). Appropriate frequency and sound amplitude have been identified as significant variables for the initiation of the reaction. On the base of first principal calculations and experimental results, the mechanism of the reaction was investigated. The relative stability of the possible intermediates has been compared, including evaluation on the ionic and radical reaction pathways for the dimerization process. Theoretical results suggested that the radical mechanism is more favorable. The C-C bond formation between the calculated radical intermediates occurs spontaneously (∆G = −214 kJ/mol for ZnCl(2), −163 kJ/mol in the case of Zn(OAc)(2)), which proves the possibility for the homodimerization of 3-acetylcoumarin via formation of radical species. Both experimental and theoretical data clarified the activation role of the solvent on the reactivity of the Zn-salt. The formation of complexes of solvent molecules with Zn-atom from the ZnCl(2) reduces the energy barrier for the dissociation of Zn-Cl bond and facilitate the formation of the dimeric product. |
format | Online Article Text |
id | pubmed-9655359 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96553592022-11-15 Experimental and Theoretical Study on the Homodimerization Mechanism of 3-Acetylcoumarin Simeonova, Kristina B. Koleva, Ana I. Zlatanova, Anna-Mariya R. Petkova-Yankova, Nevena I. Aleksandrov, Hristiyan A. Petkov, Petko St. Nikolova, Rositca D. Molecules Article In the present study, the reaction conditions for homodimerization process of 3-acetylcoumarin were achieved under sonication using combination of zinc and metallic salt (ZnCl(2) or Zn(OAc)(2)). Appropriate frequency and sound amplitude have been identified as significant variables for the initiation of the reaction. On the base of first principal calculations and experimental results, the mechanism of the reaction was investigated. The relative stability of the possible intermediates has been compared, including evaluation on the ionic and radical reaction pathways for the dimerization process. Theoretical results suggested that the radical mechanism is more favorable. The C-C bond formation between the calculated radical intermediates occurs spontaneously (∆G = −214 kJ/mol for ZnCl(2), −163 kJ/mol in the case of Zn(OAc)(2)), which proves the possibility for the homodimerization of 3-acetylcoumarin via formation of radical species. Both experimental and theoretical data clarified the activation role of the solvent on the reactivity of the Zn-salt. The formation of complexes of solvent molecules with Zn-atom from the ZnCl(2) reduces the energy barrier for the dissociation of Zn-Cl bond and facilitate the formation of the dimeric product. MDPI 2022-10-25 /pmc/articles/PMC9655359/ /pubmed/36364063 http://dx.doi.org/10.3390/molecules27217228 Text en © 2022 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 | Article Simeonova, Kristina B. Koleva, Ana I. Zlatanova, Anna-Mariya R. Petkova-Yankova, Nevena I. Aleksandrov, Hristiyan A. Petkov, Petko St. Nikolova, Rositca D. Experimental and Theoretical Study on the Homodimerization Mechanism of 3-Acetylcoumarin |
title | Experimental and Theoretical Study on the Homodimerization Mechanism of 3-Acetylcoumarin |
title_full | Experimental and Theoretical Study on the Homodimerization Mechanism of 3-Acetylcoumarin |
title_fullStr | Experimental and Theoretical Study on the Homodimerization Mechanism of 3-Acetylcoumarin |
title_full_unstemmed | Experimental and Theoretical Study on the Homodimerization Mechanism of 3-Acetylcoumarin |
title_short | Experimental and Theoretical Study on the Homodimerization Mechanism of 3-Acetylcoumarin |
title_sort | experimental and theoretical study on the homodimerization mechanism of 3-acetylcoumarin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9655359/ https://www.ncbi.nlm.nih.gov/pubmed/36364063 http://dx.doi.org/10.3390/molecules27217228 |
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