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A Molecular Nanotube with Three-Dimensional π-Conjugation**

A π-conjugated twelve-porphyrin tube is synthesized in 32 % yield by a template-directed coupling reaction that joins together six porphyrin dimers, forming twelve new C=C bonds. The nanotube has two bound templates, enclosing an internal volume of approximately 4.5 nm(3). Its UV/Vis/NIR absorption...

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Autores principales: Neuhaus, Patrik, Cnossen, Arjen, Gong, Juliane Q, Herz, Laura M, Anderson, Harry L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: WILEY-VCH Verlag 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4510782/
https://www.ncbi.nlm.nih.gov/pubmed/25950655
http://dx.doi.org/10.1002/anie.201502735
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author Neuhaus, Patrik
Cnossen, Arjen
Gong, Juliane Q
Herz, Laura M
Anderson, Harry L
author_facet Neuhaus, Patrik
Cnossen, Arjen
Gong, Juliane Q
Herz, Laura M
Anderson, Harry L
author_sort Neuhaus, Patrik
collection PubMed
description A π-conjugated twelve-porphyrin tube is synthesized in 32 % yield by a template-directed coupling reaction that joins together six porphyrin dimers, forming twelve new C=C bonds. The nanotube has two bound templates, enclosing an internal volume of approximately 4.5 nm(3). Its UV/Vis/NIR absorption and fluorescence spectra resemble those of a previously reported six-porphyrin ring, but are red-shifted by approximately 300 cm(−1), reflecting increased conjugation. Ultrafast fluorescence spectroscopy demonstrates extensive excited-state delocalization. Transfer of electronic excitation from an initially formed state polarized in the direction of the nanotube axis (z axis) to an excited state polarized in the xy plane occurs within 200 fs, resulting in a negative fluorescence anisotropy on excitation at 742 nm.
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spelling pubmed-45107822015-07-24 A Molecular Nanotube with Three-Dimensional π-Conjugation** Neuhaus, Patrik Cnossen, Arjen Gong, Juliane Q Herz, Laura M Anderson, Harry L Angew Chem Int Ed Engl Communications A π-conjugated twelve-porphyrin tube is synthesized in 32 % yield by a template-directed coupling reaction that joins together six porphyrin dimers, forming twelve new C=C bonds. The nanotube has two bound templates, enclosing an internal volume of approximately 4.5 nm(3). Its UV/Vis/NIR absorption and fluorescence spectra resemble those of a previously reported six-porphyrin ring, but are red-shifted by approximately 300 cm(−1), reflecting increased conjugation. Ultrafast fluorescence spectroscopy demonstrates extensive excited-state delocalization. Transfer of electronic excitation from an initially formed state polarized in the direction of the nanotube axis (z axis) to an excited state polarized in the xy plane occurs within 200 fs, resulting in a negative fluorescence anisotropy on excitation at 742 nm. WILEY-VCH Verlag 2015-06-15 2015-05-07 /pmc/articles/PMC4510782/ /pubmed/25950655 http://dx.doi.org/10.1002/anie.201502735 Text en © 2015 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
Neuhaus, Patrik
Cnossen, Arjen
Gong, Juliane Q
Herz, Laura M
Anderson, Harry L
A Molecular Nanotube with Three-Dimensional π-Conjugation**
title A Molecular Nanotube with Three-Dimensional π-Conjugation**
title_full A Molecular Nanotube with Three-Dimensional π-Conjugation**
title_fullStr A Molecular Nanotube with Three-Dimensional π-Conjugation**
title_full_unstemmed A Molecular Nanotube with Three-Dimensional π-Conjugation**
title_short A Molecular Nanotube with Three-Dimensional π-Conjugation**
title_sort molecular nanotube with three-dimensional π-conjugation**
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4510782/
https://www.ncbi.nlm.nih.gov/pubmed/25950655
http://dx.doi.org/10.1002/anie.201502735
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