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High Conversion of Styrene, Ethylene, and Hydrogen to Linear Monoalkylbenzenes
1-Alkylbenzenes as a precursor of surfactants, can be produced from ethylene, styrene, and hydrogen. These intermediates, lacking tertiary carbons, are environmentally more benign than commercial ones that bear the aromatic ring linked to an internal carbon of the aliphatic chain. The one-pot synthe...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6100200/ https://www.ncbi.nlm.nih.gov/pubmed/29799449 http://dx.doi.org/10.3390/molecules23061260 |
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author | Lamparelli, David Hermann Ricca, Antonio Palma, Vincenzo Oliva, Leone |
author_facet | Lamparelli, David Hermann Ricca, Antonio Palma, Vincenzo Oliva, Leone |
author_sort | Lamparelli, David Hermann |
collection | PubMed |
description | 1-Alkylbenzenes as a precursor of surfactants, can be produced from ethylene, styrene, and hydrogen. These intermediates, lacking tertiary carbons, are environmentally more benign than commercial ones that bear the aromatic ring linked to an internal carbon of the aliphatic chain. The one-pot synthesis of highly linear 1-alkylbenzenes (LABs) through the homogeneous catalysis of olefin poly-insertion from cheap and largely available reagents can be carried out with a high turnover and selectivity. A purposely designed reactor that allows for the fine control of the three components feed, along with temperature, plays a key role in this achievement. A turnover of 194 g of LABs per mmol of catalyst per hour can be obtained with the simultaneous removal of polyethylene as a by-product. |
format | Online Article Text |
id | pubmed-6100200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61002002018-11-13 High Conversion of Styrene, Ethylene, and Hydrogen to Linear Monoalkylbenzenes Lamparelli, David Hermann Ricca, Antonio Palma, Vincenzo Oliva, Leone Molecules Article 1-Alkylbenzenes as a precursor of surfactants, can be produced from ethylene, styrene, and hydrogen. These intermediates, lacking tertiary carbons, are environmentally more benign than commercial ones that bear the aromatic ring linked to an internal carbon of the aliphatic chain. The one-pot synthesis of highly linear 1-alkylbenzenes (LABs) through the homogeneous catalysis of olefin poly-insertion from cheap and largely available reagents can be carried out with a high turnover and selectivity. A purposely designed reactor that allows for the fine control of the three components feed, along with temperature, plays a key role in this achievement. A turnover of 194 g of LABs per mmol of catalyst per hour can be obtained with the simultaneous removal of polyethylene as a by-product. MDPI 2018-05-25 /pmc/articles/PMC6100200/ /pubmed/29799449 http://dx.doi.org/10.3390/molecules23061260 Text en © 2018 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Lamparelli, David Hermann Ricca, Antonio Palma, Vincenzo Oliva, Leone High Conversion of Styrene, Ethylene, and Hydrogen to Linear Monoalkylbenzenes |
title | High Conversion of Styrene, Ethylene, and Hydrogen to Linear Monoalkylbenzenes |
title_full | High Conversion of Styrene, Ethylene, and Hydrogen to Linear Monoalkylbenzenes |
title_fullStr | High Conversion of Styrene, Ethylene, and Hydrogen to Linear Monoalkylbenzenes |
title_full_unstemmed | High Conversion of Styrene, Ethylene, and Hydrogen to Linear Monoalkylbenzenes |
title_short | High Conversion of Styrene, Ethylene, and Hydrogen to Linear Monoalkylbenzenes |
title_sort | high conversion of styrene, ethylene, and hydrogen to linear monoalkylbenzenes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6100200/ https://www.ncbi.nlm.nih.gov/pubmed/29799449 http://dx.doi.org/10.3390/molecules23061260 |
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