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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
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.
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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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