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Optical Excitation of Carbon Nanotubes Drives Localized Diazonium Reactions
[Image: see text] Covalent chemistries have been widely used to modify carbon nanomaterials; however, they typically lack the precision and efficiency required to directly engineer their optical and electronic properties. Here, we show, for the first time, that visible light which is tuned into reso...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5317278/ https://www.ncbi.nlm.nih.gov/pubmed/27588432 http://dx.doi.org/10.1021/acs.jpclett.6b01771 |
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author | Powell, Lyndsey R. Piao, Yanmei Wang, YuHuang |
author_facet | Powell, Lyndsey R. Piao, Yanmei Wang, YuHuang |
author_sort | Powell, Lyndsey R. |
collection | PubMed |
description | [Image: see text] Covalent chemistries have been widely used to modify carbon nanomaterials; however, they typically lack the precision and efficiency required to directly engineer their optical and electronic properties. Here, we show, for the first time, that visible light which is tuned into resonance with carbon nanotubes can be used to drive their functionalization by aryldiazonium salts. The optical excitation accelerates the reaction rate 154-fold (±13) and makes it possible to significantly improve the efficiency of covalent bonding to the sp(2) carbon lattice. Control experiments suggest that the reaction is dominated by a localized photothermal effect. This light-driven reaction paves the way for precise nanochemistry that can directly tailor carbon nanomaterials at the optical and electronic levels. |
format | Online Article Text |
id | pubmed-5317278 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-53172782017-09-02 Optical Excitation of Carbon Nanotubes Drives Localized Diazonium Reactions Powell, Lyndsey R. Piao, Yanmei Wang, YuHuang J Phys Chem Lett [Image: see text] Covalent chemistries have been widely used to modify carbon nanomaterials; however, they typically lack the precision and efficiency required to directly engineer their optical and electronic properties. Here, we show, for the first time, that visible light which is tuned into resonance with carbon nanotubes can be used to drive their functionalization by aryldiazonium salts. The optical excitation accelerates the reaction rate 154-fold (±13) and makes it possible to significantly improve the efficiency of covalent bonding to the sp(2) carbon lattice. Control experiments suggest that the reaction is dominated by a localized photothermal effect. This light-driven reaction paves the way for precise nanochemistry that can directly tailor carbon nanomaterials at the optical and electronic levels. American Chemical Society 2016-09-02 2016-09-15 /pmc/articles/PMC5317278/ /pubmed/27588432 http://dx.doi.org/10.1021/acs.jpclett.6b01771 Text en Copyright © 2016 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Powell, Lyndsey R. Piao, Yanmei Wang, YuHuang Optical Excitation of Carbon Nanotubes Drives Localized Diazonium Reactions |
title | Optical Excitation of Carbon Nanotubes Drives Localized
Diazonium Reactions |
title_full | Optical Excitation of Carbon Nanotubes Drives Localized
Diazonium Reactions |
title_fullStr | Optical Excitation of Carbon Nanotubes Drives Localized
Diazonium Reactions |
title_full_unstemmed | Optical Excitation of Carbon Nanotubes Drives Localized
Diazonium Reactions |
title_short | Optical Excitation of Carbon Nanotubes Drives Localized
Diazonium Reactions |
title_sort | optical excitation of carbon nanotubes drives localized
diazonium reactions |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5317278/ https://www.ncbi.nlm.nih.gov/pubmed/27588432 http://dx.doi.org/10.1021/acs.jpclett.6b01771 |
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