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Single-Acetylene Linked Porphyrin Nanorings
[Image: see text] The synthesis of ethyne-linked porphyrin nanorings has been achieved by template-directed Sonogashira coupling. The cyclic hexamer and octamer are predicted by density functional theory to adopt low symmetry conformations, due to dihedral twists between neighboring porphyrin units,...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5719470/ https://www.ncbi.nlm.nih.gov/pubmed/29094947 http://dx.doi.org/10.1021/jacs.7b10710 |
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author | Rickhaus, Michel Vargas Jentzsch, Andreas Tejerina, Lara Grübner, Isabell Jirasek, Michael Claridge, Timothy D. W. Anderson, Harry L. |
author_facet | Rickhaus, Michel Vargas Jentzsch, Andreas Tejerina, Lara Grübner, Isabell Jirasek, Michael Claridge, Timothy D. W. Anderson, Harry L. |
author_sort | Rickhaus, Michel |
collection | PubMed |
description | [Image: see text] The synthesis of ethyne-linked porphyrin nanorings has been achieved by template-directed Sonogashira coupling. The cyclic hexamer and octamer are predicted by density functional theory to adopt low symmetry conformations, due to dihedral twists between neighboring porphyrin units, but their symmetries are effectively D(6h) and D(8h), respectively, in solution by (1)H NMR. The fluorescence spectra indicate that the singlet excited states of these nanorings are highly delocalized. |
format | Online Article Text |
id | pubmed-5719470 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-57194702017-12-08 Single-Acetylene Linked Porphyrin Nanorings Rickhaus, Michel Vargas Jentzsch, Andreas Tejerina, Lara Grübner, Isabell Jirasek, Michael Claridge, Timothy D. W. Anderson, Harry L. J Am Chem Soc [Image: see text] The synthesis of ethyne-linked porphyrin nanorings has been achieved by template-directed Sonogashira coupling. The cyclic hexamer and octamer are predicted by density functional theory to adopt low symmetry conformations, due to dihedral twists between neighboring porphyrin units, but their symmetries are effectively D(6h) and D(8h), respectively, in solution by (1)H NMR. The fluorescence spectra indicate that the singlet excited states of these nanorings are highly delocalized. American Chemical Society 2017-11-02 2017-11-22 /pmc/articles/PMC5719470/ /pubmed/29094947 http://dx.doi.org/10.1021/jacs.7b10710 Text en Copyright © 2017 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 | Rickhaus, Michel Vargas Jentzsch, Andreas Tejerina, Lara Grübner, Isabell Jirasek, Michael Claridge, Timothy D. W. Anderson, Harry L. Single-Acetylene Linked Porphyrin Nanorings |
title | Single-Acetylene
Linked Porphyrin Nanorings |
title_full | Single-Acetylene
Linked Porphyrin Nanorings |
title_fullStr | Single-Acetylene
Linked Porphyrin Nanorings |
title_full_unstemmed | Single-Acetylene
Linked Porphyrin Nanorings |
title_short | Single-Acetylene
Linked Porphyrin Nanorings |
title_sort | single-acetylene
linked porphyrin nanorings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5719470/ https://www.ncbi.nlm.nih.gov/pubmed/29094947 http://dx.doi.org/10.1021/jacs.7b10710 |
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