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Direct single-molecule dynamic detection of chemical reactions

Single-molecule detection can reveal time trajectories and reaction pathways of individual intermediates/transition states in chemical reactions and biological processes, which is of fundamental importance to elucidate their intrinsic mechanisms. We present a reliable, label-free single-molecule app...

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Autores principales: Guan, Jianxin, Jia, Chuancheng, Li, Yanwei, Liu, Zitong, Wang, Jinying, Yang, Zhongyue, Gu, Chunhui, Su, Dingkai, Houk, Kendall N., Zhang, Deqing, Guo, Xuefeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5817934/
https://www.ncbi.nlm.nih.gov/pubmed/29487914
http://dx.doi.org/10.1126/sciadv.aar2177
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author Guan, Jianxin
Jia, Chuancheng
Li, Yanwei
Liu, Zitong
Wang, Jinying
Yang, Zhongyue
Gu, Chunhui
Su, Dingkai
Houk, Kendall N.
Zhang, Deqing
Guo, Xuefeng
author_facet Guan, Jianxin
Jia, Chuancheng
Li, Yanwei
Liu, Zitong
Wang, Jinying
Yang, Zhongyue
Gu, Chunhui
Su, Dingkai
Houk, Kendall N.
Zhang, Deqing
Guo, Xuefeng
author_sort Guan, Jianxin
collection PubMed
description Single-molecule detection can reveal time trajectories and reaction pathways of individual intermediates/transition states in chemical reactions and biological processes, which is of fundamental importance to elucidate their intrinsic mechanisms. We present a reliable, label-free single-molecule approach that allows us to directly explore the dynamic process of basic chemical reactions at the single-event level by using stable graphene-molecule single-molecule junctions. These junctions are constructed by covalently connecting a single molecule with a 9-fluorenone center to nanogapped graphene electrodes. For the first time, real-time single-molecule electrical measurements unambiguously show reproducible large-amplitude two-level fluctuations that are highly dependent on solvent environments in a nucleophilic addition reaction of hydroxylamine to a carbonyl group. Both theoretical simulations and ensemble experiments prove that this observation originates from the reversible transition between the reactant and a new intermediate state within a time scale of a few microseconds. These investigations open up a new route that is able to be immediately applied to probe fast single-molecule physics or biophysics with high time resolution, making an important contribution to broad fields beyond reaction chemistry.
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spelling pubmed-58179342018-02-27 Direct single-molecule dynamic detection of chemical reactions Guan, Jianxin Jia, Chuancheng Li, Yanwei Liu, Zitong Wang, Jinying Yang, Zhongyue Gu, Chunhui Su, Dingkai Houk, Kendall N. Zhang, Deqing Guo, Xuefeng Sci Adv Research Articles Single-molecule detection can reveal time trajectories and reaction pathways of individual intermediates/transition states in chemical reactions and biological processes, which is of fundamental importance to elucidate their intrinsic mechanisms. We present a reliable, label-free single-molecule approach that allows us to directly explore the dynamic process of basic chemical reactions at the single-event level by using stable graphene-molecule single-molecule junctions. These junctions are constructed by covalently connecting a single molecule with a 9-fluorenone center to nanogapped graphene electrodes. For the first time, real-time single-molecule electrical measurements unambiguously show reproducible large-amplitude two-level fluctuations that are highly dependent on solvent environments in a nucleophilic addition reaction of hydroxylamine to a carbonyl group. Both theoretical simulations and ensemble experiments prove that this observation originates from the reversible transition between the reactant and a new intermediate state within a time scale of a few microseconds. These investigations open up a new route that is able to be immediately applied to probe fast single-molecule physics or biophysics with high time resolution, making an important contribution to broad fields beyond reaction chemistry. American Association for the Advancement of Science 2018-02-09 /pmc/articles/PMC5817934/ /pubmed/29487914 http://dx.doi.org/10.1126/sciadv.aar2177 Text en Copyright © 2018 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Guan, Jianxin
Jia, Chuancheng
Li, Yanwei
Liu, Zitong
Wang, Jinying
Yang, Zhongyue
Gu, Chunhui
Su, Dingkai
Houk, Kendall N.
Zhang, Deqing
Guo, Xuefeng
Direct single-molecule dynamic detection of chemical reactions
title Direct single-molecule dynamic detection of chemical reactions
title_full Direct single-molecule dynamic detection of chemical reactions
title_fullStr Direct single-molecule dynamic detection of chemical reactions
title_full_unstemmed Direct single-molecule dynamic detection of chemical reactions
title_short Direct single-molecule dynamic detection of chemical reactions
title_sort direct single-molecule dynamic detection of chemical reactions
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5817934/
https://www.ncbi.nlm.nih.gov/pubmed/29487914
http://dx.doi.org/10.1126/sciadv.aar2177
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