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Effects of Bentonite on p-Methoxybenzyl Acetate: A Theoretical Model for Oligomerization via an Electrophilic-Substitution Mechanism
Tonsil Actisil FF, a commercial bentonitic clay, promotes the formation of a series of electrophilic-aromatic-substitution products from para-methoxybenzyl acetate in carbon disulfide. The molecules obtained correspond to linear isomeric dimers, trimers, tetramers and a pentamer, according to their...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259743/ https://www.ncbi.nlm.nih.gov/pubmed/21339711 http://dx.doi.org/10.3390/molecules16021761 |
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author | Salmón, Manuel Miranda, Rene Nicolás-Vázquez, Ines Vargas-Rodriguez, Yolanda Marina Cruz-Borbolla, Julian Medrano, María Isabel Morales-Serna, José Antonio |
author_facet | Salmón, Manuel Miranda, Rene Nicolás-Vázquez, Ines Vargas-Rodriguez, Yolanda Marina Cruz-Borbolla, Julian Medrano, María Isabel Morales-Serna, José Antonio |
author_sort | Salmón, Manuel |
collection | PubMed |
description | Tonsil Actisil FF, a commercial bentonitic clay, promotes the formation of a series of electrophilic-aromatic-substitution products from para-methoxybenzyl acetate in carbon disulfide. The molecules obtained correspond to linear isomeric dimers, trimers, tetramers and a pentamer, according to their spectroscopic data. A clear indication of the title mechanistic pathway for the oligomerization growth was obtained from the analysis of a set of computational-chemistry calculations using the density-functional-theory level B3LYP/6-311++G(d,p). The corresponding conclusions were based on the computed dipole moments, the HOMO/LUMO distributions, and a natural-populations analysis of the studied molecules. |
format | Online Article Text |
id | pubmed-6259743 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62597432018-12-20 Effects of Bentonite on p-Methoxybenzyl Acetate: A Theoretical Model for Oligomerization via an Electrophilic-Substitution Mechanism Salmón, Manuel Miranda, Rene Nicolás-Vázquez, Ines Vargas-Rodriguez, Yolanda Marina Cruz-Borbolla, Julian Medrano, María Isabel Morales-Serna, José Antonio Molecules Article Tonsil Actisil FF, a commercial bentonitic clay, promotes the formation of a series of electrophilic-aromatic-substitution products from para-methoxybenzyl acetate in carbon disulfide. The molecules obtained correspond to linear isomeric dimers, trimers, tetramers and a pentamer, according to their spectroscopic data. A clear indication of the title mechanistic pathway for the oligomerization growth was obtained from the analysis of a set of computational-chemistry calculations using the density-functional-theory level B3LYP/6-311++G(d,p). The corresponding conclusions were based on the computed dipole moments, the HOMO/LUMO distributions, and a natural-populations analysis of the studied molecules. MDPI 2011-02-21 /pmc/articles/PMC6259743/ /pubmed/21339711 http://dx.doi.org/10.3390/molecules16021761 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Salmón, Manuel Miranda, Rene Nicolás-Vázquez, Ines Vargas-Rodriguez, Yolanda Marina Cruz-Borbolla, Julian Medrano, María Isabel Morales-Serna, José Antonio Effects of Bentonite on p-Methoxybenzyl Acetate: A Theoretical Model for Oligomerization via an Electrophilic-Substitution Mechanism |
title | Effects of Bentonite on p-Methoxybenzyl Acetate: A Theoretical Model for Oligomerization via an Electrophilic-Substitution Mechanism |
title_full | Effects of Bentonite on p-Methoxybenzyl Acetate: A Theoretical Model for Oligomerization via an Electrophilic-Substitution Mechanism |
title_fullStr | Effects of Bentonite on p-Methoxybenzyl Acetate: A Theoretical Model for Oligomerization via an Electrophilic-Substitution Mechanism |
title_full_unstemmed | Effects of Bentonite on p-Methoxybenzyl Acetate: A Theoretical Model for Oligomerization via an Electrophilic-Substitution Mechanism |
title_short | Effects of Bentonite on p-Methoxybenzyl Acetate: A Theoretical Model for Oligomerization via an Electrophilic-Substitution Mechanism |
title_sort | effects of bentonite on p-methoxybenzyl acetate: a theoretical model for oligomerization via an electrophilic-substitution mechanism |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259743/ https://www.ncbi.nlm.nih.gov/pubmed/21339711 http://dx.doi.org/10.3390/molecules16021761 |
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