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Cooperative assembly of H-bonded rosettes inside a porphyrin nanoring
The melamine·barbiturate H-bonded rosette motif is of comparable dimensions and symmetry to the cavity of a butadiyne-linked 6-porphyrin nanoring. Functionalisation of each of the barbiturate components and the pyrimidine components of a H-bonded rosette with a pyridine ligand leads to a self-assemb...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8179033/ https://www.ncbi.nlm.nih.gov/pubmed/34163905 http://dx.doi.org/10.1039/d0sc06097f |
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author | Motloch, Petr Bols, Pernille S. Anderson, Harry L. Hunter, Christopher A. |
author_facet | Motloch, Petr Bols, Pernille S. Anderson, Harry L. Hunter, Christopher A. |
author_sort | Motloch, Petr |
collection | PubMed |
description | The melamine·barbiturate H-bonded rosette motif is of comparable dimensions and symmetry to the cavity of a butadiyne-linked 6-porphyrin nanoring. Functionalisation of each of the barbiturate components and the pyrimidine components of a H-bonded rosette with a pyridine ligand leads to a self-assembled hexapyridine ligand, which binds cooperatively to the zinc porphyrin nanoring. UV-vis-NIR and (1)H NMR experiments show that the 7-component assembly forms at concentrations at which neither the H-bonding interactions nor the zinc porphyrin–pyridine interactions are formed in the absence of one of the three components. The mean effective molarities of these rosette complexes are around 200 mM in chloroform at 298 K. |
format | Online Article Text |
id | pubmed-8179033 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-81790332021-06-22 Cooperative assembly of H-bonded rosettes inside a porphyrin nanoring Motloch, Petr Bols, Pernille S. Anderson, Harry L. Hunter, Christopher A. Chem Sci Chemistry The melamine·barbiturate H-bonded rosette motif is of comparable dimensions and symmetry to the cavity of a butadiyne-linked 6-porphyrin nanoring. Functionalisation of each of the barbiturate components and the pyrimidine components of a H-bonded rosette with a pyridine ligand leads to a self-assembled hexapyridine ligand, which binds cooperatively to the zinc porphyrin nanoring. UV-vis-NIR and (1)H NMR experiments show that the 7-component assembly forms at concentrations at which neither the H-bonding interactions nor the zinc porphyrin–pyridine interactions are formed in the absence of one of the three components. The mean effective molarities of these rosette complexes are around 200 mM in chloroform at 298 K. The Royal Society of Chemistry 2020-12-08 /pmc/articles/PMC8179033/ /pubmed/34163905 http://dx.doi.org/10.1039/d0sc06097f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Motloch, Petr Bols, Pernille S. Anderson, Harry L. Hunter, Christopher A. Cooperative assembly of H-bonded rosettes inside a porphyrin nanoring |
title | Cooperative assembly of H-bonded rosettes inside a porphyrin nanoring |
title_full | Cooperative assembly of H-bonded rosettes inside a porphyrin nanoring |
title_fullStr | Cooperative assembly of H-bonded rosettes inside a porphyrin nanoring |
title_full_unstemmed | Cooperative assembly of H-bonded rosettes inside a porphyrin nanoring |
title_short | Cooperative assembly of H-bonded rosettes inside a porphyrin nanoring |
title_sort | cooperative assembly of h-bonded rosettes inside a porphyrin nanoring |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8179033/ https://www.ncbi.nlm.nih.gov/pubmed/34163905 http://dx.doi.org/10.1039/d0sc06097f |
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