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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,...

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Autores principales: Rickhaus, Michel, Vargas Jentzsch, Andreas, Tejerina, Lara, Grübner, Isabell, Jirasek, Michael, Claridge, Timothy D. W., Anderson, Harry L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
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.
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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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