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A Divergent Alkyne Diol Directs [2 + 2] Photoreactivity in the Solid State: Cocrystal, Supramolecular Catalysis, and Sublimation Effects
2-butyne-1,4-diol (1,4-bd) is used as a divergent ditopic template that directs trans-1,2-bis (n-pyridyl) ethylene (n,n′-bpe, where n = n′ = 3 or 4) to undergo an intermolecular [2 + 2] photodimerization in the solid state. The components of cocrystals [(1,4-bd)·(4,4′-bpe)](n) and [(1,4-bd)·(3,3′-bp...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6749457/ https://www.ncbi.nlm.nih.gov/pubmed/31443541 http://dx.doi.org/10.3390/molecules24173059 |
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author | Oburn, Shalisa M. Quentin, Jay MacGillivray, Leonard R. |
author_facet | Oburn, Shalisa M. Quentin, Jay MacGillivray, Leonard R. |
author_sort | Oburn, Shalisa M. |
collection | PubMed |
description | 2-butyne-1,4-diol (1,4-bd) is used as a divergent ditopic template that directs trans-1,2-bis (n-pyridyl) ethylene (n,n′-bpe, where n = n′ = 3 or 4) to undergo an intermolecular [2 + 2] photodimerization in the solid state. The components of cocrystals [(1,4-bd)·(4,4′-bpe)](n) and [(1,4-bd)·(3,3′-bpe)](n) form 1D hydrogen-bonded polymers with n,n′-bpe assembled as infinite parallel stacks. The alkenes undergo [2 + 2] photocycloadditions to form rctt-tetrakis (n-pyridyl) cyclobutane (where n = 3 or 4). We demonstrate that the reactive solid involving 4,4′-bpe exhibits supramolecular catalysis. |
format | Online Article Text |
id | pubmed-6749457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-67494572019-09-27 A Divergent Alkyne Diol Directs [2 + 2] Photoreactivity in the Solid State: Cocrystal, Supramolecular Catalysis, and Sublimation Effects Oburn, Shalisa M. Quentin, Jay MacGillivray, Leonard R. Molecules Article 2-butyne-1,4-diol (1,4-bd) is used as a divergent ditopic template that directs trans-1,2-bis (n-pyridyl) ethylene (n,n′-bpe, where n = n′ = 3 or 4) to undergo an intermolecular [2 + 2] photodimerization in the solid state. The components of cocrystals [(1,4-bd)·(4,4′-bpe)](n) and [(1,4-bd)·(3,3′-bpe)](n) form 1D hydrogen-bonded polymers with n,n′-bpe assembled as infinite parallel stacks. The alkenes undergo [2 + 2] photocycloadditions to form rctt-tetrakis (n-pyridyl) cyclobutane (where n = 3 or 4). We demonstrate that the reactive solid involving 4,4′-bpe exhibits supramolecular catalysis. MDPI 2019-08-22 /pmc/articles/PMC6749457/ /pubmed/31443541 http://dx.doi.org/10.3390/molecules24173059 Text en © 2019 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 Oburn, Shalisa M. Quentin, Jay MacGillivray, Leonard R. A Divergent Alkyne Diol Directs [2 + 2] Photoreactivity in the Solid State: Cocrystal, Supramolecular Catalysis, and Sublimation Effects |
title | A Divergent Alkyne Diol Directs [2 + 2] Photoreactivity in the Solid State: Cocrystal, Supramolecular Catalysis, and Sublimation Effects |
title_full | A Divergent Alkyne Diol Directs [2 + 2] Photoreactivity in the Solid State: Cocrystal, Supramolecular Catalysis, and Sublimation Effects |
title_fullStr | A Divergent Alkyne Diol Directs [2 + 2] Photoreactivity in the Solid State: Cocrystal, Supramolecular Catalysis, and Sublimation Effects |
title_full_unstemmed | A Divergent Alkyne Diol Directs [2 + 2] Photoreactivity in the Solid State: Cocrystal, Supramolecular Catalysis, and Sublimation Effects |
title_short | A Divergent Alkyne Diol Directs [2 + 2] Photoreactivity in the Solid State: Cocrystal, Supramolecular Catalysis, and Sublimation Effects |
title_sort | divergent alkyne diol directs [2 + 2] photoreactivity in the solid state: cocrystal, supramolecular catalysis, and sublimation effects |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6749457/ https://www.ncbi.nlm.nih.gov/pubmed/31443541 http://dx.doi.org/10.3390/molecules24173059 |
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