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Two-Photon-Induced [2 + 2] Cycloaddition of Bis-thymines: A Biocompatible and Reversible Approach
[Image: see text] Despite having great value across a wide variety of scientific fields, two-photon polymerizations currently suffer from two significant problems: the need for photoinitiators, which generate toxic side products, and the irreversibility of the process. Hence, the design of a versati...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7254774/ https://www.ncbi.nlm.nih.gov/pubmed/32478244 http://dx.doi.org/10.1021/acsomega.0c00770 |
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author | Ricci, Monica Rutten, Martin G.T.A. Toyouchi, Shuichi Nanayakkara, Sepa Fortuni, Beatrice Vitale, Raffaele Rocha, Susana Wilson, Daniela A. Hofkens, Johan Saito, Kei Uji-i, Hiroshi |
author_facet | Ricci, Monica Rutten, Martin G.T.A. Toyouchi, Shuichi Nanayakkara, Sepa Fortuni, Beatrice Vitale, Raffaele Rocha, Susana Wilson, Daniela A. Hofkens, Johan Saito, Kei Uji-i, Hiroshi |
author_sort | Ricci, Monica |
collection | PubMed |
description | [Image: see text] Despite having great value across a wide variety of scientific fields, two-photon polymerizations currently suffer from two significant problems: the need for photoinitiators, which generate toxic side products, and the irreversibility of the process. Hence, the design of a versatile approach that circumvents these issues represents a major scientific challenge. Herein, we report a two-photon absorption strategy where reversible [2 + 2] cycloaddition of bis-thymines was achieved without the need for any photoinitiator. The cycloaddition and cycloreversion reactions could be induced by simply changing the irradiation wavelength, and repeated writing and erasing cycles were performed. The simplicity, reversibility, and biocompatibility of this strategy open up a whole new toolbox for applications across a wide variety of scientific fields. |
format | Online Article Text |
id | pubmed-7254774 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-72547742020-05-29 Two-Photon-Induced [2 + 2] Cycloaddition of Bis-thymines: A Biocompatible and Reversible Approach Ricci, Monica Rutten, Martin G.T.A. Toyouchi, Shuichi Nanayakkara, Sepa Fortuni, Beatrice Vitale, Raffaele Rocha, Susana Wilson, Daniela A. Hofkens, Johan Saito, Kei Uji-i, Hiroshi ACS Omega [Image: see text] Despite having great value across a wide variety of scientific fields, two-photon polymerizations currently suffer from two significant problems: the need for photoinitiators, which generate toxic side products, and the irreversibility of the process. Hence, the design of a versatile approach that circumvents these issues represents a major scientific challenge. Herein, we report a two-photon absorption strategy where reversible [2 + 2] cycloaddition of bis-thymines was achieved without the need for any photoinitiator. The cycloaddition and cycloreversion reactions could be induced by simply changing the irradiation wavelength, and repeated writing and erasing cycles were performed. The simplicity, reversibility, and biocompatibility of this strategy open up a whole new toolbox for applications across a wide variety of scientific fields. American Chemical Society 2020-05-12 /pmc/articles/PMC7254774/ /pubmed/32478244 http://dx.doi.org/10.1021/acsomega.0c00770 Text en Copyright © 2020 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Ricci, Monica Rutten, Martin G.T.A. Toyouchi, Shuichi Nanayakkara, Sepa Fortuni, Beatrice Vitale, Raffaele Rocha, Susana Wilson, Daniela A. Hofkens, Johan Saito, Kei Uji-i, Hiroshi Two-Photon-Induced [2 + 2] Cycloaddition of Bis-thymines: A Biocompatible and Reversible Approach |
title | Two-Photon-Induced [2 + 2] Cycloaddition of Bis-thymines:
A Biocompatible and Reversible Approach |
title_full | Two-Photon-Induced [2 + 2] Cycloaddition of Bis-thymines:
A Biocompatible and Reversible Approach |
title_fullStr | Two-Photon-Induced [2 + 2] Cycloaddition of Bis-thymines:
A Biocompatible and Reversible Approach |
title_full_unstemmed | Two-Photon-Induced [2 + 2] Cycloaddition of Bis-thymines:
A Biocompatible and Reversible Approach |
title_short | Two-Photon-Induced [2 + 2] Cycloaddition of Bis-thymines:
A Biocompatible and Reversible Approach |
title_sort | two-photon-induced [2 + 2] cycloaddition of bis-thymines:
a biocompatible and reversible approach |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7254774/ https://www.ncbi.nlm.nih.gov/pubmed/32478244 http://dx.doi.org/10.1021/acsomega.0c00770 |
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