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STM-induced ring closure of vinylheptafulvene molecular dipole switches on Au(111)

Dihydroazulene/vinylheptafulvene pairs are known as molecular dipole switches that undergo a ring-opening/-closure reaction by UV irradiation or thermal excitation. Herein, we show that the ring-closure reaction of a single vinylheptafulvene adsorbed on the Au(111) surface can be induced by voltage...

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Autores principales: Au-Yeung, Kwan Ho, Kühne, Tim, Aiboudi, Oumaima, Sarkar, Suchetana, Guskova, Olga, Ryndyk, Dmitry A., Heine, Thomas, Lissel, Franziska, Moresco, Francesca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: RSC 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9552919/
https://www.ncbi.nlm.nih.gov/pubmed/36321147
http://dx.doi.org/10.1039/d2na00038e
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author Au-Yeung, Kwan Ho
Kühne, Tim
Aiboudi, Oumaima
Sarkar, Suchetana
Guskova, Olga
Ryndyk, Dmitry A.
Heine, Thomas
Lissel, Franziska
Moresco, Francesca
author_facet Au-Yeung, Kwan Ho
Kühne, Tim
Aiboudi, Oumaima
Sarkar, Suchetana
Guskova, Olga
Ryndyk, Dmitry A.
Heine, Thomas
Lissel, Franziska
Moresco, Francesca
author_sort Au-Yeung, Kwan Ho
collection PubMed
description Dihydroazulene/vinylheptafulvene pairs are known as molecular dipole switches that undergo a ring-opening/-closure reaction by UV irradiation or thermal excitation. Herein, we show that the ring-closure reaction of a single vinylheptafulvene adsorbed on the Au(111) surface can be induced by voltage pulses from the tip of a scanning tunneling microscope. This cyclization is accompanied by the elimination of HCN, as confirmed by simulations. When inducing lateral movements by applying voltage pulses with the STM tip, we observe that the response of the single molecules changes with the ring closing reaction. This behaviour is discussed by comparing the dipole moment and the charge distribution of the open and closed forms on the surface.
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spelling pubmed-95529192022-10-31 STM-induced ring closure of vinylheptafulvene molecular dipole switches on Au(111) Au-Yeung, Kwan Ho Kühne, Tim Aiboudi, Oumaima Sarkar, Suchetana Guskova, Olga Ryndyk, Dmitry A. Heine, Thomas Lissel, Franziska Moresco, Francesca Nanoscale Adv Chemistry Dihydroazulene/vinylheptafulvene pairs are known as molecular dipole switches that undergo a ring-opening/-closure reaction by UV irradiation or thermal excitation. Herein, we show that the ring-closure reaction of a single vinylheptafulvene adsorbed on the Au(111) surface can be induced by voltage pulses from the tip of a scanning tunneling microscope. This cyclization is accompanied by the elimination of HCN, as confirmed by simulations. When inducing lateral movements by applying voltage pulses with the STM tip, we observe that the response of the single molecules changes with the ring closing reaction. This behaviour is discussed by comparing the dipole moment and the charge distribution of the open and closed forms on the surface. RSC 2022-09-20 /pmc/articles/PMC9552919/ /pubmed/36321147 http://dx.doi.org/10.1039/d2na00038e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Au-Yeung, Kwan Ho
Kühne, Tim
Aiboudi, Oumaima
Sarkar, Suchetana
Guskova, Olga
Ryndyk, Dmitry A.
Heine, Thomas
Lissel, Franziska
Moresco, Francesca
STM-induced ring closure of vinylheptafulvene molecular dipole switches on Au(111)
title STM-induced ring closure of vinylheptafulvene molecular dipole switches on Au(111)
title_full STM-induced ring closure of vinylheptafulvene molecular dipole switches on Au(111)
title_fullStr STM-induced ring closure of vinylheptafulvene molecular dipole switches on Au(111)
title_full_unstemmed STM-induced ring closure of vinylheptafulvene molecular dipole switches on Au(111)
title_short STM-induced ring closure of vinylheptafulvene molecular dipole switches on Au(111)
title_sort stm-induced ring closure of vinylheptafulvene molecular dipole switches on au(111)
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9552919/
https://www.ncbi.nlm.nih.gov/pubmed/36321147
http://dx.doi.org/10.1039/d2na00038e
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