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Ester formation at the liquid–solid interface
A chemical reaction (esterification) within a molecular monolayer at the liquid–solid interface without any catalyst was studied using ambient scanning tunneling microscopy. The monolayer consisted of a regular array of two species, an organic acid (trimesic acid) and an alcohol (undecan-1-ol or dec...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5647715/ https://www.ncbi.nlm.nih.gov/pubmed/29090115 http://dx.doi.org/10.3762/bjnano.8.213 |
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author | T. N. Ha, Nguyen Gopakumar, Thiruvancheril G D. C. Yen, Nguyen Mende, Carola Smykalla, Lars Schlesinger, Maik Buschbeck, Roy Rüffer, Tobias Lang, Heinrich Mehring, Michael Hietschold, Michael |
author_facet | T. N. Ha, Nguyen Gopakumar, Thiruvancheril G D. C. Yen, Nguyen Mende, Carola Smykalla, Lars Schlesinger, Maik Buschbeck, Roy Rüffer, Tobias Lang, Heinrich Mehring, Michael Hietschold, Michael |
author_sort | T. N. Ha, Nguyen |
collection | PubMed |
description | A chemical reaction (esterification) within a molecular monolayer at the liquid–solid interface without any catalyst was studied using ambient scanning tunneling microscopy. The monolayer consisted of a regular array of two species, an organic acid (trimesic acid) and an alcohol (undecan-1-ol or decan-1-ol), coadsorbed out of a solution of the acid within the alcohol at the interface of highly oriented pyrolytic graphite (HOPG) (0001) substrate. The monoester was observed promptly after reaching a threshold either related to the increased packing density of the adsorbate layer (which can be controlled by the concentration of the trimesic acid within the alcoholic solution via sonication or extended stirring) or by reaching a threshold with regards to the deposition temperature. Evidence that esterification takes place directly at the liquid–solid interface was strongly supported. |
format | Online Article Text |
id | pubmed-5647715 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-56477152017-10-31 Ester formation at the liquid–solid interface T. N. Ha, Nguyen Gopakumar, Thiruvancheril G D. C. Yen, Nguyen Mende, Carola Smykalla, Lars Schlesinger, Maik Buschbeck, Roy Rüffer, Tobias Lang, Heinrich Mehring, Michael Hietschold, Michael Beilstein J Nanotechnol Full Research Paper A chemical reaction (esterification) within a molecular monolayer at the liquid–solid interface without any catalyst was studied using ambient scanning tunneling microscopy. The monolayer consisted of a regular array of two species, an organic acid (trimesic acid) and an alcohol (undecan-1-ol or decan-1-ol), coadsorbed out of a solution of the acid within the alcohol at the interface of highly oriented pyrolytic graphite (HOPG) (0001) substrate. The monoester was observed promptly after reaching a threshold either related to the increased packing density of the adsorbate layer (which can be controlled by the concentration of the trimesic acid within the alcoholic solution via sonication or extended stirring) or by reaching a threshold with regards to the deposition temperature. Evidence that esterification takes place directly at the liquid–solid interface was strongly supported. Beilstein-Institut 2017-10-12 /pmc/articles/PMC5647715/ /pubmed/29090115 http://dx.doi.org/10.3762/bjnano.8.213 Text en Copyright © 2017, T. N. Ha et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjnano/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Nanotechnology terms and conditions: (https://www.beilstein-journals.org/bjnano/terms) |
spellingShingle | Full Research Paper T. N. Ha, Nguyen Gopakumar, Thiruvancheril G D. C. Yen, Nguyen Mende, Carola Smykalla, Lars Schlesinger, Maik Buschbeck, Roy Rüffer, Tobias Lang, Heinrich Mehring, Michael Hietschold, Michael Ester formation at the liquid–solid interface |
title | Ester formation at the liquid–solid interface |
title_full | Ester formation at the liquid–solid interface |
title_fullStr | Ester formation at the liquid–solid interface |
title_full_unstemmed | Ester formation at the liquid–solid interface |
title_short | Ester formation at the liquid–solid interface |
title_sort | ester formation at the liquid–solid interface |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5647715/ https://www.ncbi.nlm.nih.gov/pubmed/29090115 http://dx.doi.org/10.3762/bjnano.8.213 |
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