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Self-Assembled Bimetallic Aluminum-Salen Catalyst for the Cyclic Carbonates Synthesis
Bimetallic bis-urea functionalized salen-aluminum catalysts have been developed for cyclic carbonate synthesis from epoxides and CO(2). The urea moiety provides a bimetallic scaffold through hydrogen bonding, which expedites the cyclic carbonate formation reaction under mild reaction conditions. The...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8271522/ https://www.ncbi.nlm.nih.gov/pubmed/34279436 http://dx.doi.org/10.3390/molecules26134097 |
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author | Seong, Wooyong Hahm, Hyungwoo Kim, Seyong Park, Jongwoo Abboud, Khalil A. Hong, Sukwon |
author_facet | Seong, Wooyong Hahm, Hyungwoo Kim, Seyong Park, Jongwoo Abboud, Khalil A. Hong, Sukwon |
author_sort | Seong, Wooyong |
collection | PubMed |
description | Bimetallic bis-urea functionalized salen-aluminum catalysts have been developed for cyclic carbonate synthesis from epoxides and CO(2). The urea moiety provides a bimetallic scaffold through hydrogen bonding, which expedites the cyclic carbonate formation reaction under mild reaction conditions. The turnover frequency (TOF) of the bis-urea salen Al catalyst is three times higher than that of a μ-oxo-bridged catalyst, and 13 times higher than that of a monomeric salen aluminum catalyst. The bimetallic reaction pathway is suggested based on urea additive studies and kinetic studies. Additionally, the X-ray crystal structure of a bis-urea salen Ni complex supports the self-assembly of the bis-urea salen metal complex through hydrogen bonding. |
format | Online Article Text |
id | pubmed-8271522 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-82715222021-07-11 Self-Assembled Bimetallic Aluminum-Salen Catalyst for the Cyclic Carbonates Synthesis Seong, Wooyong Hahm, Hyungwoo Kim, Seyong Park, Jongwoo Abboud, Khalil A. Hong, Sukwon Molecules Communication Bimetallic bis-urea functionalized salen-aluminum catalysts have been developed for cyclic carbonate synthesis from epoxides and CO(2). The urea moiety provides a bimetallic scaffold through hydrogen bonding, which expedites the cyclic carbonate formation reaction under mild reaction conditions. The turnover frequency (TOF) of the bis-urea salen Al catalyst is three times higher than that of a μ-oxo-bridged catalyst, and 13 times higher than that of a monomeric salen aluminum catalyst. The bimetallic reaction pathway is suggested based on urea additive studies and kinetic studies. Additionally, the X-ray crystal structure of a bis-urea salen Ni complex supports the self-assembly of the bis-urea salen metal complex through hydrogen bonding. MDPI 2021-07-05 /pmc/articles/PMC8271522/ /pubmed/34279436 http://dx.doi.org/10.3390/molecules26134097 Text en © 2021 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 | Communication Seong, Wooyong Hahm, Hyungwoo Kim, Seyong Park, Jongwoo Abboud, Khalil A. Hong, Sukwon Self-Assembled Bimetallic Aluminum-Salen Catalyst for the Cyclic Carbonates Synthesis |
title | Self-Assembled Bimetallic Aluminum-Salen Catalyst for the Cyclic Carbonates Synthesis |
title_full | Self-Assembled Bimetallic Aluminum-Salen Catalyst for the Cyclic Carbonates Synthesis |
title_fullStr | Self-Assembled Bimetallic Aluminum-Salen Catalyst for the Cyclic Carbonates Synthesis |
title_full_unstemmed | Self-Assembled Bimetallic Aluminum-Salen Catalyst for the Cyclic Carbonates Synthesis |
title_short | Self-Assembled Bimetallic Aluminum-Salen Catalyst for the Cyclic Carbonates Synthesis |
title_sort | self-assembled bimetallic aluminum-salen catalyst for the cyclic carbonates synthesis |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8271522/ https://www.ncbi.nlm.nih.gov/pubmed/34279436 http://dx.doi.org/10.3390/molecules26134097 |
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