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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2018
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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. |
format | Online Article Text |
id | pubmed-5817934 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
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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