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Self‐Assembly of Bowl‐Shaped Naphthalimide‐Annulated Corannulene

The self‐assembly of a bowl‐shaped naphthalimide‐annulated corannulene of high solubility has been studied in a variety of solvents by NMR and UV/Vis spectroscopy. Evaluation by the anti‐cooperative K (2)‐K model revealed the formation of supramolecular dimers of outstanding thermodynamic stability....

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Detalles Bibliográficos
Autores principales: Renner, Rebecca, Stolte, Matthias, Würthner, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6946951/
https://www.ncbi.nlm.nih.gov/pubmed/31921543
http://dx.doi.org/10.1002/open.201900291
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author Renner, Rebecca
Stolte, Matthias
Würthner, Frank
author_facet Renner, Rebecca
Stolte, Matthias
Würthner, Frank
author_sort Renner, Rebecca
collection PubMed
description The self‐assembly of a bowl‐shaped naphthalimide‐annulated corannulene of high solubility has been studied in a variety of solvents by NMR and UV/Vis spectroscopy. Evaluation by the anti‐cooperative K (2)‐K model revealed the formation of supramolecular dimers of outstanding thermodynamic stability. Further structural proof for the almost exclusive formation of dimers over extended aggregates is demonstrated by atomic force microscopy (AFM) and diffusion ordered spectroscopy (DOSY) measurements as well as by theoretical calculations. Thus, herein we present the first report of a supramolecular dimer of an annulated corannulene derivative in solution and discuss its extraordinarily high thermodynamic stability with association constants up to >10(6) M(−1) in methylcyclohexane, which is comparable to the association constants given for planar phthalocyanine and perylene bisimide dyes.
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spelling pubmed-69469512020-01-09 Self‐Assembly of Bowl‐Shaped Naphthalimide‐Annulated Corannulene Renner, Rebecca Stolte, Matthias Würthner, Frank ChemistryOpen Full Papers The self‐assembly of a bowl‐shaped naphthalimide‐annulated corannulene of high solubility has been studied in a variety of solvents by NMR and UV/Vis spectroscopy. Evaluation by the anti‐cooperative K (2)‐K model revealed the formation of supramolecular dimers of outstanding thermodynamic stability. Further structural proof for the almost exclusive formation of dimers over extended aggregates is demonstrated by atomic force microscopy (AFM) and diffusion ordered spectroscopy (DOSY) measurements as well as by theoretical calculations. Thus, herein we present the first report of a supramolecular dimer of an annulated corannulene derivative in solution and discuss its extraordinarily high thermodynamic stability with association constants up to >10(6) M(−1) in methylcyclohexane, which is comparable to the association constants given for planar phthalocyanine and perylene bisimide dyes. John Wiley and Sons Inc. 2019-11-05 /pmc/articles/PMC6946951/ /pubmed/31921543 http://dx.doi.org/10.1002/open.201900291 Text en ©2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Full Papers
Renner, Rebecca
Stolte, Matthias
Würthner, Frank
Self‐Assembly of Bowl‐Shaped Naphthalimide‐Annulated Corannulene
title Self‐Assembly of Bowl‐Shaped Naphthalimide‐Annulated Corannulene
title_full Self‐Assembly of Bowl‐Shaped Naphthalimide‐Annulated Corannulene
title_fullStr Self‐Assembly of Bowl‐Shaped Naphthalimide‐Annulated Corannulene
title_full_unstemmed Self‐Assembly of Bowl‐Shaped Naphthalimide‐Annulated Corannulene
title_short Self‐Assembly of Bowl‐Shaped Naphthalimide‐Annulated Corannulene
title_sort self‐assembly of bowl‐shaped naphthalimide‐annulated corannulene
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6946951/
https://www.ncbi.nlm.nih.gov/pubmed/31921543
http://dx.doi.org/10.1002/open.201900291
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