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Construction of hexabenzocoronene-based chiral nanographenes
The past decade witnessed remarkable success in synthetic molecular nanographenes. Encouraged by the widespread application of chiral nanomaterials, the design, and construction of chiral nanographenes is a hot topic recently. As a classic nanographene unit, hexa-peri-hexabenzocoronene generally ser...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Beilstein-Institut
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241098/ https://www.ncbi.nlm.nih.gov/pubmed/37284588 http://dx.doi.org/10.3762/bjoc.19.54 |
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author | Li, Ranran Wang, Di Li, Shengtao An, Peng |
author_facet | Li, Ranran Wang, Di Li, Shengtao An, Peng |
author_sort | Li, Ranran |
collection | PubMed |
description | The past decade witnessed remarkable success in synthetic molecular nanographenes. Encouraged by the widespread application of chiral nanomaterials, the design, and construction of chiral nanographenes is a hot topic recently. As a classic nanographene unit, hexa-peri-hexabenzocoronene generally serves as the building block for nanographene synthesis. This review summarizes the representative examples of hexa-peri-hexabenzocoronene-based chiral nanographenes. |
format | Online Article Text |
id | pubmed-10241098 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-102410982023-06-06 Construction of hexabenzocoronene-based chiral nanographenes Li, Ranran Wang, Di Li, Shengtao An, Peng Beilstein J Org Chem Review The past decade witnessed remarkable success in synthetic molecular nanographenes. Encouraged by the widespread application of chiral nanomaterials, the design, and construction of chiral nanographenes is a hot topic recently. As a classic nanographene unit, hexa-peri-hexabenzocoronene generally serves as the building block for nanographene synthesis. This review summarizes the representative examples of hexa-peri-hexabenzocoronene-based chiral nanographenes. Beilstein-Institut 2023-05-30 /pmc/articles/PMC10241098/ /pubmed/37284588 http://dx.doi.org/10.3762/bjoc.19.54 Text en Copyright © 2023, Li et al. https://creativecommons.org/licenses/by/4.0/This is an open access article licensed under the terms of the Beilstein-Institut Open Access License Agreement (https://www.beilstein-journals.org/bjoc/terms/terms), which is identical to the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ). The reuse of material under this license requires that the author(s), source and license are credited. Third-party material in this article could be subject to other licenses (typically indicated in the credit line), and in this case, users are required to obtain permission from the license holder to reuse the material. |
spellingShingle | Review Li, Ranran Wang, Di Li, Shengtao An, Peng Construction of hexabenzocoronene-based chiral nanographenes |
title | Construction of hexabenzocoronene-based chiral nanographenes |
title_full | Construction of hexabenzocoronene-based chiral nanographenes |
title_fullStr | Construction of hexabenzocoronene-based chiral nanographenes |
title_full_unstemmed | Construction of hexabenzocoronene-based chiral nanographenes |
title_short | Construction of hexabenzocoronene-based chiral nanographenes |
title_sort | construction of hexabenzocoronene-based chiral nanographenes |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241098/ https://www.ncbi.nlm.nih.gov/pubmed/37284588 http://dx.doi.org/10.3762/bjoc.19.54 |
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