Cargando…
On-surface synthesis of planar π-extended [12]cycloparaphenylene
[n]cycloparaphenylenes feature extensive para-conjugation that leads to useful electronic and optoelectronic properties, but their strained topology prevents their conversion into planar macrocycles. Now, on-surface coupling of cleverly designed precursors affords planar π-extended [12]cycloparaphen...
Autor principal: | |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9814935/ https://www.ncbi.nlm.nih.gov/pubmed/36698016 http://dx.doi.org/10.1038/s42004-022-00720-5 |
_version_ | 1784864248200953856 |
---|---|
author | Richards, Victoria |
author_facet | Richards, Victoria |
author_sort | Richards, Victoria |
collection | PubMed |
description | [n]cycloparaphenylenes feature extensive para-conjugation that leads to useful electronic and optoelectronic properties, but their strained topology prevents their conversion into planar macrocycles. Now, on-surface coupling of cleverly designed precursors affords planar π-extended [12]cycloparaphenylene. |
format | Online Article Text |
id | pubmed-9814935 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98149352023-01-10 On-surface synthesis of planar π-extended [12]cycloparaphenylene Richards, Victoria Commun Chem Research Highlight [n]cycloparaphenylenes feature extensive para-conjugation that leads to useful electronic and optoelectronic properties, but their strained topology prevents their conversion into planar macrocycles. Now, on-surface coupling of cleverly designed precursors affords planar π-extended [12]cycloparaphenylene. Nature Publishing Group UK 2022-08-22 /pmc/articles/PMC9814935/ /pubmed/36698016 http://dx.doi.org/10.1038/s42004-022-00720-5 Text en © Springer Nature Limited 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Highlight Richards, Victoria On-surface synthesis of planar π-extended [12]cycloparaphenylene |
title | On-surface synthesis of planar π-extended [12]cycloparaphenylene |
title_full | On-surface synthesis of planar π-extended [12]cycloparaphenylene |
title_fullStr | On-surface synthesis of planar π-extended [12]cycloparaphenylene |
title_full_unstemmed | On-surface synthesis of planar π-extended [12]cycloparaphenylene |
title_short | On-surface synthesis of planar π-extended [12]cycloparaphenylene |
title_sort | on-surface synthesis of planar π-extended [12]cycloparaphenylene |
topic | Research Highlight |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9814935/ https://www.ncbi.nlm.nih.gov/pubmed/36698016 http://dx.doi.org/10.1038/s42004-022-00720-5 |
work_keys_str_mv | AT richardsvictoria onsurfacesynthesisofplanarpextended12cycloparaphenylene |