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Substituted 1,3,5-Triazine Hexacarboxylates as Potential Linkers for MOFs
Hexacarboxylates are promising linkers for MOFs such as NU-109 or NU-110, which possess large values for surfaces and pore volumina. Starting from 2,4,6-tris(bromoaryl)-1,3,5-triazines, palladium-catalyzed cross coupling reactions (Suzuki-Miyaura, Sonogashira-Hagihara) form elongated hexacarboxylate...
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/PMC6804050/ https://www.ncbi.nlm.nih.gov/pubmed/31557929 http://dx.doi.org/10.3390/molecules24193480 |
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author | Klinkebiel, Arne Beyer, Ole Lüning, Ulrich |
author_facet | Klinkebiel, Arne Beyer, Ole Lüning, Ulrich |
author_sort | Klinkebiel, Arne |
collection | PubMed |
description | Hexacarboxylates are promising linkers for MOFs such as NU-109 or NU-110, which possess large values for surfaces and pore volumina. Starting from 2,4,6-tris(bromoaryl)-1,3,5-triazines, palladium-catalyzed cross coupling reactions (Suzuki-Miyaura, Sonogashira-Hagihara) form elongated hexacarboxylate linkers. Eight new 2,4,6-tris(biphenyl) and 2,4,6-tris(phenylethynylphenyl) 1,3,5-triazines have been prepared in quantities ranging from 40 mg to 1.1 g. In five cases, one of the arms of the linker carries an additional functionality (NO(2) or OMe). |
format | Online Article Text |
id | pubmed-6804050 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-68040502019-11-18 Substituted 1,3,5-Triazine Hexacarboxylates as Potential Linkers for MOFs Klinkebiel, Arne Beyer, Ole Lüning, Ulrich Molecules Article Hexacarboxylates are promising linkers for MOFs such as NU-109 or NU-110, which possess large values for surfaces and pore volumina. Starting from 2,4,6-tris(bromoaryl)-1,3,5-triazines, palladium-catalyzed cross coupling reactions (Suzuki-Miyaura, Sonogashira-Hagihara) form elongated hexacarboxylate linkers. Eight new 2,4,6-tris(biphenyl) and 2,4,6-tris(phenylethynylphenyl) 1,3,5-triazines have been prepared in quantities ranging from 40 mg to 1.1 g. In five cases, one of the arms of the linker carries an additional functionality (NO(2) or OMe). MDPI 2019-09-25 /pmc/articles/PMC6804050/ /pubmed/31557929 http://dx.doi.org/10.3390/molecules24193480 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 Klinkebiel, Arne Beyer, Ole Lüning, Ulrich Substituted 1,3,5-Triazine Hexacarboxylates as Potential Linkers for MOFs |
title | Substituted 1,3,5-Triazine Hexacarboxylates as Potential Linkers for MOFs |
title_full | Substituted 1,3,5-Triazine Hexacarboxylates as Potential Linkers for MOFs |
title_fullStr | Substituted 1,3,5-Triazine Hexacarboxylates as Potential Linkers for MOFs |
title_full_unstemmed | Substituted 1,3,5-Triazine Hexacarboxylates as Potential Linkers for MOFs |
title_short | Substituted 1,3,5-Triazine Hexacarboxylates as Potential Linkers for MOFs |
title_sort | substituted 1,3,5-triazine hexacarboxylates as potential linkers for mofs |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6804050/ https://www.ncbi.nlm.nih.gov/pubmed/31557929 http://dx.doi.org/10.3390/molecules24193480 |
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