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Porphene and porphite as porphyrin analogs of graphene and graphite
Two-dimensional materials have unusual properties and promise applications in nanoelectronics, spintronics, photonics, (electro)catalysis, separations, and elsewhere. Most are inorganic and their properties are difficult to tune. Here we report the preparation of Zn porphene, a member of the previou...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10562370/ https://www.ncbi.nlm.nih.gov/pubmed/37813887 http://dx.doi.org/10.1038/s41467-023-41461-w |
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author | Magnera, Thomas F. Dron, Paul I. Bozzone, Jared P. Jovanovic, Milena Rončević, Igor Tortorici, Edward Bu, Wei Miller, Elisa M. Rogers, Charles T. Michl, Josef |
author_facet | Magnera, Thomas F. Dron, Paul I. Bozzone, Jared P. Jovanovic, Milena Rončević, Igor Tortorici, Edward Bu, Wei Miller, Elisa M. Rogers, Charles T. Michl, Josef |
author_sort | Magnera, Thomas F. |
collection | PubMed |
description | Two-dimensional materials have unusual properties and promise applications in nanoelectronics, spintronics, photonics, (electro)catalysis, separations, and elsewhere. Most are inorganic and their properties are difficult to tune. Here we report the preparation of Zn porphene, a member of the previously only hypothetical organic metalloporphene family. Similar to graphene, these also are fully conjugated two-dimensional polymers, but are composed of fused metalloporphyrin rings. Zn porphene is synthesized on water surface by two-dimensional oxidative polymerization of a Langmuir layer of Zn porphyrin with K(2)IrCl(6), reminiscent of known one-dimensional polymerization of pyrroles. It is transferable to other substrates and bridges μm-sized pits. Contrary to previous theoretical predictions of metallic conductivity, it is a p-type semiconductor due to a predicted Peierls distortion of its unit cell from square to rectangular, analogous to the appearance of bond-length alternation in antiaromatic molecules. The observed reversible insertion of various metal ions, possibly carrying a fifth or sixth ligand, promises tunability and even patterning of circuits on an atomic canvas without removing any π centers from conjugation. |
format | Online Article Text |
id | pubmed-10562370 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105623702023-10-11 Porphene and porphite as porphyrin analogs of graphene and graphite Magnera, Thomas F. Dron, Paul I. Bozzone, Jared P. Jovanovic, Milena Rončević, Igor Tortorici, Edward Bu, Wei Miller, Elisa M. Rogers, Charles T. Michl, Josef Nat Commun Article Two-dimensional materials have unusual properties and promise applications in nanoelectronics, spintronics, photonics, (electro)catalysis, separations, and elsewhere. Most are inorganic and their properties are difficult to tune. Here we report the preparation of Zn porphene, a member of the previously only hypothetical organic metalloporphene family. Similar to graphene, these also are fully conjugated two-dimensional polymers, but are composed of fused metalloporphyrin rings. Zn porphene is synthesized on water surface by two-dimensional oxidative polymerization of a Langmuir layer of Zn porphyrin with K(2)IrCl(6), reminiscent of known one-dimensional polymerization of pyrroles. It is transferable to other substrates and bridges μm-sized pits. Contrary to previous theoretical predictions of metallic conductivity, it is a p-type semiconductor due to a predicted Peierls distortion of its unit cell from square to rectangular, analogous to the appearance of bond-length alternation in antiaromatic molecules. The observed reversible insertion of various metal ions, possibly carrying a fifth or sixth ligand, promises tunability and even patterning of circuits on an atomic canvas without removing any π centers from conjugation. Nature Publishing Group UK 2023-10-09 /pmc/articles/PMC10562370/ /pubmed/37813887 http://dx.doi.org/10.1038/s41467-023-41461-w Text en © The Author(s) 2023 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 | Article Magnera, Thomas F. Dron, Paul I. Bozzone, Jared P. Jovanovic, Milena Rončević, Igor Tortorici, Edward Bu, Wei Miller, Elisa M. Rogers, Charles T. Michl, Josef Porphene and porphite as porphyrin analogs of graphene and graphite |
title | Porphene and porphite as porphyrin analogs of graphene and graphite |
title_full | Porphene and porphite as porphyrin analogs of graphene and graphite |
title_fullStr | Porphene and porphite as porphyrin analogs of graphene and graphite |
title_full_unstemmed | Porphene and porphite as porphyrin analogs of graphene and graphite |
title_short | Porphene and porphite as porphyrin analogs of graphene and graphite |
title_sort | porphene and porphite as porphyrin analogs of graphene and graphite |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10562370/ https://www.ncbi.nlm.nih.gov/pubmed/37813887 http://dx.doi.org/10.1038/s41467-023-41461-w |
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