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Conjugated Nanohoops Incorporating Donor, Acceptor, Hetero‐ or Polycyclic Aromatics

In the last 13 years several synthetic strategies were developed that provide access to [n]cycloparaphenylenes ([n]CPPs) and related conjugated nanohoops. A number of potential applications emerged, including optoelectronic devices, and their use as templates for carbon nanomaterials and in supramol...

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Detalles Bibliográficos
Autores principales: Hermann, Mathias, Wassy, Daniel, Esser, Birgit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9542246/
https://www.ncbi.nlm.nih.gov/pubmed/32902109
http://dx.doi.org/10.1002/anie.202007024
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author Hermann, Mathias
Wassy, Daniel
Esser, Birgit
author_facet Hermann, Mathias
Wassy, Daniel
Esser, Birgit
author_sort Hermann, Mathias
collection PubMed
description In the last 13 years several synthetic strategies were developed that provide access to [n]cycloparaphenylenes ([n]CPPs) and related conjugated nanohoops. A number of potential applications emerged, including optoelectronic devices, and their use as templates for carbon nanomaterials and in supramolecular chemistry. To tune the structural or optoelectronic properties of carbon nanohoops beyond the size‐dependent effect known for [n]CPPs, a variety of aromatic rings other than benzene were introduced. In this Review, we provide an overview of the syntheses, properties, and applications of conjugated nanohoops beyond [n]CPPs with intrinsic donor/acceptor structure or such that contain acceptor, donor, heteroaromatic or polycyclic aromatic units within the hoop as well as conjugated nanobelts.
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spelling pubmed-95422462022-10-14 Conjugated Nanohoops Incorporating Donor, Acceptor, Hetero‐ or Polycyclic Aromatics Hermann, Mathias Wassy, Daniel Esser, Birgit Angew Chem Int Ed Engl Reviews In the last 13 years several synthetic strategies were developed that provide access to [n]cycloparaphenylenes ([n]CPPs) and related conjugated nanohoops. A number of potential applications emerged, including optoelectronic devices, and their use as templates for carbon nanomaterials and in supramolecular chemistry. To tune the structural or optoelectronic properties of carbon nanohoops beyond the size‐dependent effect known for [n]CPPs, a variety of aromatic rings other than benzene were introduced. In this Review, we provide an overview of the syntheses, properties, and applications of conjugated nanohoops beyond [n]CPPs with intrinsic donor/acceptor structure or such that contain acceptor, donor, heteroaromatic or polycyclic aromatic units within the hoop as well as conjugated nanobelts. John Wiley and Sons Inc. 2021-03-22 2021-07-12 /pmc/articles/PMC9542246/ /pubmed/32902109 http://dx.doi.org/10.1002/anie.202007024 Text en © 2020 The Authors. Published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Hermann, Mathias
Wassy, Daniel
Esser, Birgit
Conjugated Nanohoops Incorporating Donor, Acceptor, Hetero‐ or Polycyclic Aromatics
title Conjugated Nanohoops Incorporating Donor, Acceptor, Hetero‐ or Polycyclic Aromatics
title_full Conjugated Nanohoops Incorporating Donor, Acceptor, Hetero‐ or Polycyclic Aromatics
title_fullStr Conjugated Nanohoops Incorporating Donor, Acceptor, Hetero‐ or Polycyclic Aromatics
title_full_unstemmed Conjugated Nanohoops Incorporating Donor, Acceptor, Hetero‐ or Polycyclic Aromatics
title_short Conjugated Nanohoops Incorporating Donor, Acceptor, Hetero‐ or Polycyclic Aromatics
title_sort conjugated nanohoops incorporating donor, acceptor, hetero‐ or polycyclic aromatics
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9542246/
https://www.ncbi.nlm.nih.gov/pubmed/32902109
http://dx.doi.org/10.1002/anie.202007024
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