Cargando…
Highly-conducting molecular circuits based on antiaromaticity
Aromaticity is a fundamental concept in chemistry. It is described by Hückel’s rule that states that a cyclic planar π-system is aromatic when it shares 4n+2 π-electrons and antiaromatic when it possesses 4n π-electrons. Antiaromatic compounds are predicted to exhibit remarkable charge transport pro...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5524926/ https://www.ncbi.nlm.nih.gov/pubmed/28722006 http://dx.doi.org/10.1038/ncomms15984 |
_version_ | 1783252553113272320 |
---|---|
author | Fujii, Shintaro Marqués-González, Santiago Shin, Ji-Young Shinokubo, Hiroshi Masuda, Takuya Nishino, Tomoaki Arasu, Narendra P. Vázquez, Héctor Kiguchi, Manabu |
author_facet | Fujii, Shintaro Marqués-González, Santiago Shin, Ji-Young Shinokubo, Hiroshi Masuda, Takuya Nishino, Tomoaki Arasu, Narendra P. Vázquez, Héctor Kiguchi, Manabu |
author_sort | Fujii, Shintaro |
collection | PubMed |
description | Aromaticity is a fundamental concept in chemistry. It is described by Hückel’s rule that states that a cyclic planar π-system is aromatic when it shares 4n+2 π-electrons and antiaromatic when it possesses 4n π-electrons. Antiaromatic compounds are predicted to exhibit remarkable charge transport properties and high redox activities. However, it has so far only been possible to measure compounds with reduced aromaticity but not antiaromatic species due to their energetic instability. Here, we address these issues by investigating the single-molecule charge transport properties of a genuinely antiaromatic compound, showing that antiaromaticity results in an order of magnitude increase in conductance compared with the aromatic counterpart. Single-molecule current–voltage measurements and ab initio transport calculations reveal that this results from a reduced energy gap and a frontier molecular resonance closer to the Fermi level in the antiaromatic species. The conductance of the antiaromatic complex is further modulated electrochemically, demonstrating its potential as a high-conductance transistor. |
format | Online Article Text |
id | pubmed-5524926 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-55249262017-07-28 Highly-conducting molecular circuits based on antiaromaticity Fujii, Shintaro Marqués-González, Santiago Shin, Ji-Young Shinokubo, Hiroshi Masuda, Takuya Nishino, Tomoaki Arasu, Narendra P. Vázquez, Héctor Kiguchi, Manabu Nat Commun Article Aromaticity is a fundamental concept in chemistry. It is described by Hückel’s rule that states that a cyclic planar π-system is aromatic when it shares 4n+2 π-electrons and antiaromatic when it possesses 4n π-electrons. Antiaromatic compounds are predicted to exhibit remarkable charge transport properties and high redox activities. However, it has so far only been possible to measure compounds with reduced aromaticity but not antiaromatic species due to their energetic instability. Here, we address these issues by investigating the single-molecule charge transport properties of a genuinely antiaromatic compound, showing that antiaromaticity results in an order of magnitude increase in conductance compared with the aromatic counterpart. Single-molecule current–voltage measurements and ab initio transport calculations reveal that this results from a reduced energy gap and a frontier molecular resonance closer to the Fermi level in the antiaromatic species. The conductance of the antiaromatic complex is further modulated electrochemically, demonstrating its potential as a high-conductance transistor. Nature Publishing Group 2017-07-19 /pmc/articles/PMC5524926/ /pubmed/28722006 http://dx.doi.org/10.1038/ncomms15984 Text en Copyright © 2017, The Author(s) http://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/ |
spellingShingle | Article Fujii, Shintaro Marqués-González, Santiago Shin, Ji-Young Shinokubo, Hiroshi Masuda, Takuya Nishino, Tomoaki Arasu, Narendra P. Vázquez, Héctor Kiguchi, Manabu Highly-conducting molecular circuits based on antiaromaticity |
title | Highly-conducting molecular circuits based on antiaromaticity |
title_full | Highly-conducting molecular circuits based on antiaromaticity |
title_fullStr | Highly-conducting molecular circuits based on antiaromaticity |
title_full_unstemmed | Highly-conducting molecular circuits based on antiaromaticity |
title_short | Highly-conducting molecular circuits based on antiaromaticity |
title_sort | highly-conducting molecular circuits based on antiaromaticity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5524926/ https://www.ncbi.nlm.nih.gov/pubmed/28722006 http://dx.doi.org/10.1038/ncomms15984 |
work_keys_str_mv | AT fujiishintaro highlyconductingmolecularcircuitsbasedonantiaromaticity AT marquesgonzalezsantiago highlyconductingmolecularcircuitsbasedonantiaromaticity AT shinjiyoung highlyconductingmolecularcircuitsbasedonantiaromaticity AT shinokubohiroshi highlyconductingmolecularcircuitsbasedonantiaromaticity AT masudatakuya highlyconductingmolecularcircuitsbasedonantiaromaticity AT nishinotomoaki highlyconductingmolecularcircuitsbasedonantiaromaticity AT arasunarendrap highlyconductingmolecularcircuitsbasedonantiaromaticity AT vazquezhector highlyconductingmolecularcircuitsbasedonantiaromaticity AT kiguchimanabu highlyconductingmolecularcircuitsbasedonantiaromaticity |