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...

Descripción completa

Detalles Bibliográficos
Autores principales: Fujii, Shintaro, Marqués-González, Santiago, Shin, Ji-Young, Shinokubo, Hiroshi, Masuda, Takuya, Nishino, Tomoaki, Arasu, Narendra P., Vázquez, Héctor, Kiguchi, Manabu
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