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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...

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Autores principales: Lamparelli, David Hermann, Ricca, Antonio, Palma, Vincenzo, Oliva, Leone
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
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.
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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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