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Synthesis of Metallomacrocycle and Coordination Polymers with Pyridine‐Based Amidocarboxylate Ligands and Their Catalytic Activities towards the Henry and Knoevenagel Reactions
The reactions of 3,3′‐{(pyridine‐2,6‐dicarbonyl)bis(azanediyl)}dibenzoic acid (H(2)L) with zinc(II), cadmium(II), and samarium(III) nitrates were studied, and the obtained compounds, [Zn(1κO:2κO′‐L)(H(2)O)(2)](n) (1), [Cd(1κO (2):2κO (2)‐L)(H(2)O)(2)](2) ⋅6n H(2)O⋅ n C(4)H(8)O(2) ⋅1.5n DMF (2), and...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6217112/ https://www.ncbi.nlm.nih.gov/pubmed/30410851 http://dx.doi.org/10.1002/open.201800170 |
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author | Karmakar, Anirban Rúbio, Guilherme M. D. M. Guedes da Silva, M. Fátima C. Pombeiro, Armando J. L. |
author_facet | Karmakar, Anirban Rúbio, Guilherme M. D. M. Guedes da Silva, M. Fátima C. Pombeiro, Armando J. L. |
author_sort | Karmakar, Anirban |
collection | PubMed |
description | The reactions of 3,3′‐{(pyridine‐2,6‐dicarbonyl)bis(azanediyl)}dibenzoic acid (H(2)L) with zinc(II), cadmium(II), and samarium(III) nitrates were studied, and the obtained compounds, [Zn(1κO:2κO′‐L)(H(2)O)(2)](n) (1), [Cd(1κO (2):2κO (2)‐L)(H(2)O)(2)](2) ⋅6n H(2)O⋅ n C(4)H(8)O(2) ⋅1.5n DMF (2), and [Sm(1κO:2κO′O′′:3κO′′′‐L)(NO(3))(H(2)O)(dmf)](n) ⋅ n DMF (3), were characterized by elemental analysis, FTIR spectroscopy, thermogravimetric analysis, and X‐ray single‐crystal diffraction. Compounds 1 and 3 have 1D zigzag‐ and double‐chain‐type structures, respectively, whereas 2 features a dinuclear metallomacrocyclic complex. The ligand (L(2−)) orients in different conformations, that is, syn‐syn for 1 and anti‐anti for 2 and 3. Compound 1 is the first example in which the syn‐syn conformation for this ligand has been observed. These compounds act as heterogeneous catalysts for the nitroaldol (Henry; in water medium) and Knoevenagel condensation reactions of different aldehydes, and the most effective is zinc coordination polymer 1. Recyclability, heterogeneity, and size‐selectivity tests were performed, which showed that the catalyst was highly active over at least four recycling runs. |
format | Online Article Text |
id | pubmed-6217112 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62171122018-11-08 Synthesis of Metallomacrocycle and Coordination Polymers with Pyridine‐Based Amidocarboxylate Ligands and Their Catalytic Activities towards the Henry and Knoevenagel Reactions Karmakar, Anirban Rúbio, Guilherme M. D. M. Guedes da Silva, M. Fátima C. Pombeiro, Armando J. L. ChemistryOpen Full Papers The reactions of 3,3′‐{(pyridine‐2,6‐dicarbonyl)bis(azanediyl)}dibenzoic acid (H(2)L) with zinc(II), cadmium(II), and samarium(III) nitrates were studied, and the obtained compounds, [Zn(1κO:2κO′‐L)(H(2)O)(2)](n) (1), [Cd(1κO (2):2κO (2)‐L)(H(2)O)(2)](2) ⋅6n H(2)O⋅ n C(4)H(8)O(2) ⋅1.5n DMF (2), and [Sm(1κO:2κO′O′′:3κO′′′‐L)(NO(3))(H(2)O)(dmf)](n) ⋅ n DMF (3), were characterized by elemental analysis, FTIR spectroscopy, thermogravimetric analysis, and X‐ray single‐crystal diffraction. Compounds 1 and 3 have 1D zigzag‐ and double‐chain‐type structures, respectively, whereas 2 features a dinuclear metallomacrocyclic complex. The ligand (L(2−)) orients in different conformations, that is, syn‐syn for 1 and anti‐anti for 2 and 3. Compound 1 is the first example in which the syn‐syn conformation for this ligand has been observed. These compounds act as heterogeneous catalysts for the nitroaldol (Henry; in water medium) and Knoevenagel condensation reactions of different aldehydes, and the most effective is zinc coordination polymer 1. Recyclability, heterogeneity, and size‐selectivity tests were performed, which showed that the catalyst was highly active over at least four recycling runs. John Wiley and Sons Inc. 2018-11-05 /pmc/articles/PMC6217112/ /pubmed/30410851 http://dx.doi.org/10.1002/open.201800170 Text en © 2018 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Full Papers Karmakar, Anirban Rúbio, Guilherme M. D. M. Guedes da Silva, M. Fátima C. Pombeiro, Armando J. L. Synthesis of Metallomacrocycle and Coordination Polymers with Pyridine‐Based Amidocarboxylate Ligands and Their Catalytic Activities towards the Henry and Knoevenagel Reactions |
title | Synthesis of Metallomacrocycle and Coordination Polymers with Pyridine‐Based Amidocarboxylate Ligands and Their Catalytic Activities towards the Henry and Knoevenagel Reactions |
title_full | Synthesis of Metallomacrocycle and Coordination Polymers with Pyridine‐Based Amidocarboxylate Ligands and Their Catalytic Activities towards the Henry and Knoevenagel Reactions |
title_fullStr | Synthesis of Metallomacrocycle and Coordination Polymers with Pyridine‐Based Amidocarboxylate Ligands and Their Catalytic Activities towards the Henry and Knoevenagel Reactions |
title_full_unstemmed | Synthesis of Metallomacrocycle and Coordination Polymers with Pyridine‐Based Amidocarboxylate Ligands and Their Catalytic Activities towards the Henry and Knoevenagel Reactions |
title_short | Synthesis of Metallomacrocycle and Coordination Polymers with Pyridine‐Based Amidocarboxylate Ligands and Their Catalytic Activities towards the Henry and Knoevenagel Reactions |
title_sort | synthesis of metallomacrocycle and coordination polymers with pyridine‐based amidocarboxylate ligands and their catalytic activities towards the henry and knoevenagel reactions |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6217112/ https://www.ncbi.nlm.nih.gov/pubmed/30410851 http://dx.doi.org/10.1002/open.201800170 |
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