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Facile Supramolecular Engineering of Porphyrin cis Tautomers: The Case of β-Octabromo-meso-tetraarylporphyrins
[Image: see text] A porphyrin cis tautomer, where the two central NH protons are on adjacent pyrrole rings, has long been invoked as an intermediate in porphyrin tautomerism. Only recently, however, has such a species been isolated and structurally characterized. Thus, single-crystal X-ray structure...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7178774/ https://www.ncbi.nlm.nih.gov/pubmed/32337452 http://dx.doi.org/10.1021/acsomega.0c00517 |
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author | Thomas, Kolle E. Slebodnick, Carla Ghosh, Abhik |
author_facet | Thomas, Kolle E. Slebodnick, Carla Ghosh, Abhik |
author_sort | Thomas, Kolle E. |
collection | PubMed |
description | [Image: see text] A porphyrin cis tautomer, where the two central NH protons are on adjacent pyrrole rings, has long been invoked as an intermediate in porphyrin tautomerism. Only recently, however, has such a species been isolated and structurally characterized. Thus, single-crystal X-ray structure determinations of two highly saddled free-base porphyrins, β-heptakis(trifluoromethyl)-meso-tetrakis(p-fluorophenyl)porphyrin, H(2)[(CF(3))(7)TFPP], and β-octaiodo-5,10,15,20-tetrakis(4′-trifluoromethylphenyl)porphyrin, H(2)[I(8)TCF(3)PP], unambiguously revealed cis tautomeric structures, each stabilized as a termolecular complex with a pair of ROH (R = CH(3) or H) molecules that form hydrogen-bonded N–H···O–H···N straps connecting the central NH groups with the antipodal unprotonated nitrogens. The unusual substitution patterns of these two porphyrins, however, have left open the question how readily such supramolecular assemblies might be engineered, which prompted us to examine the much more synthetically accessible β-octabromo-meso-tetraphenylporphyrins. Herein, single-crystal X-ray structures were obtained for two such compounds, 2,3,7,8,12,13,17,18-octabromo-5,10,15,20-tetrakis(4′-trifluoromethylphenyl)porphyrin, H(2)[Br(8)TCF(3)PP], and 2,3,7,8,12,13,17,18-octabromo-5,10,15,20-tetrakis(4′-fluorophenyl)porphyrin, H(2)[Br(8)TFPP], and although the central hydrogens could not all be located unambiguously, the electron density could be convincingly modeled as porphyrin cis tautomers, existing in each case as a bis-methanol adduct. In addition, a perusal of the Cambridge Structural Database suggests that there may well be additional examples of porphyrin cis tautomers that have not been recognized as such. We are therefore increasingly confident that porphyrin cis tautomers are readily accessible via supramolecular engineering, involving the simple stratagem of crystallizing a strongly saddled porphyrin from a solvent system containing an amphiprotic species such as water or an alcohol. |
format | Online Article Text |
id | pubmed-7178774 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-71787742020-04-24 Facile Supramolecular Engineering of Porphyrin cis Tautomers: The Case of β-Octabromo-meso-tetraarylporphyrins Thomas, Kolle E. Slebodnick, Carla Ghosh, Abhik ACS Omega [Image: see text] A porphyrin cis tautomer, where the two central NH protons are on adjacent pyrrole rings, has long been invoked as an intermediate in porphyrin tautomerism. Only recently, however, has such a species been isolated and structurally characterized. Thus, single-crystal X-ray structure determinations of two highly saddled free-base porphyrins, β-heptakis(trifluoromethyl)-meso-tetrakis(p-fluorophenyl)porphyrin, H(2)[(CF(3))(7)TFPP], and β-octaiodo-5,10,15,20-tetrakis(4′-trifluoromethylphenyl)porphyrin, H(2)[I(8)TCF(3)PP], unambiguously revealed cis tautomeric structures, each stabilized as a termolecular complex with a pair of ROH (R = CH(3) or H) molecules that form hydrogen-bonded N–H···O–H···N straps connecting the central NH groups with the antipodal unprotonated nitrogens. The unusual substitution patterns of these two porphyrins, however, have left open the question how readily such supramolecular assemblies might be engineered, which prompted us to examine the much more synthetically accessible β-octabromo-meso-tetraphenylporphyrins. Herein, single-crystal X-ray structures were obtained for two such compounds, 2,3,7,8,12,13,17,18-octabromo-5,10,15,20-tetrakis(4′-trifluoromethylphenyl)porphyrin, H(2)[Br(8)TCF(3)PP], and 2,3,7,8,12,13,17,18-octabromo-5,10,15,20-tetrakis(4′-fluorophenyl)porphyrin, H(2)[Br(8)TFPP], and although the central hydrogens could not all be located unambiguously, the electron density could be convincingly modeled as porphyrin cis tautomers, existing in each case as a bis-methanol adduct. In addition, a perusal of the Cambridge Structural Database suggests that there may well be additional examples of porphyrin cis tautomers that have not been recognized as such. We are therefore increasingly confident that porphyrin cis tautomers are readily accessible via supramolecular engineering, involving the simple stratagem of crystallizing a strongly saddled porphyrin from a solvent system containing an amphiprotic species such as water or an alcohol. American Chemical Society 2020-04-02 /pmc/articles/PMC7178774/ /pubmed/32337452 http://dx.doi.org/10.1021/acsomega.0c00517 Text en Copyright © 2020 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Thomas, Kolle E. Slebodnick, Carla Ghosh, Abhik Facile Supramolecular Engineering of Porphyrin cis Tautomers: The Case of β-Octabromo-meso-tetraarylporphyrins |
title | Facile Supramolecular Engineering of Porphyrin cis
Tautomers: The Case of β-Octabromo-meso-tetraarylporphyrins |
title_full | Facile Supramolecular Engineering of Porphyrin cis
Tautomers: The Case of β-Octabromo-meso-tetraarylporphyrins |
title_fullStr | Facile Supramolecular Engineering of Porphyrin cis
Tautomers: The Case of β-Octabromo-meso-tetraarylporphyrins |
title_full_unstemmed | Facile Supramolecular Engineering of Porphyrin cis
Tautomers: The Case of β-Octabromo-meso-tetraarylporphyrins |
title_short | Facile Supramolecular Engineering of Porphyrin cis
Tautomers: The Case of β-Octabromo-meso-tetraarylporphyrins |
title_sort | facile supramolecular engineering of porphyrin cis
tautomers: the case of β-octabromo-meso-tetraarylporphyrins |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7178774/ https://www.ncbi.nlm.nih.gov/pubmed/32337452 http://dx.doi.org/10.1021/acsomega.0c00517 |
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