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Two-Photon-Induced [2+2] Cycloaddition of Bis-thymines: A Biocompatible and Reversible Approach
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Title: | Two-Photon-Induced [2+2] Cycloaddition of Bis-thymines: A Biocompatible and Reversible Approach |
Authors: | Ricci, Monica Browse this author | Rutten, Martin G. T. A. Browse this author | Toyouchi, Shuichi Browse this author | Nanayakkara, Sepa Browse this author | Fortuni, Beatrice Browse this author | Vitale, Raffaele Browse this author | Rocha, Susana Browse this author | Wilson, Daniela A. Browse this author | Hofkens, Johan Browse this author | Saito, Kei Browse this author | Uji-I, Hiroshi Browse this author →KAKEN DB |
Issue Date: | 26-May-2020 |
Publisher: | American Chemical Society |
Journal Title: | ACS Omega |
Volume: | 5 |
Issue: | 20 |
Start Page: | 11547 |
End Page: | 11552 |
Publisher DOI: | 10.1021/acsomega.0c00770 |
Abstract: | 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. |
Rights: | Copyright © 2020 American Chemical Society | https://creativecommons.org/licenses/by-nc-nd/4.0/ |
Type: | article |
URI: | http://hdl.handle.net/2115/78933 |
Appears in Collections: | 電子科学研究所 (Research Institute for Electronic Science) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)
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