Synergistic Two‐Color Photochemical Polymer Network Formation and Lithography

Abstract We introduce synergistic two‐color lithography as an advanced wavelength‐gated strategy for spatially and temporally controlling polymer network formation. Our photoresist entails two photoswitches, i.e., diarylindenone epoxide (DIO) and strained azobenzene (SA), each activated at a judiciously selected wavelength, i.e., 375 or 430 nm. Under specific conditions of photon flux, simultaneous irradiation at both wavelengths induces a (3 + 2) cycloaddition between the photoactivated DIO′ and SA′ species, generating covalently crosslinked networks, whereas under these specifically determined conditions, single‐wavelength exposure does not induce solidification. Kinetic analysis highlights the potential of synergistic activation to enable advanced additive manufacturing. We implemented the two‐color activated covalent bond forming system in a dual‐laser lithographic platform enabling the fabrication of well‐defined structures, including segmented ring and butterfly architectures by simply activating and deactivating one of the colors of light.

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Publication Details

Journal
Angewandte Chemie
Published
2025-10-03
DOI
https://doi.org/10.1002/ange.202518815
Primary Topic
Photochromic and Fluorescence Chemistry
Type
article
Field-Weighted Citation Impact
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article

Synergistic Two‐Color Photochemical Polymer Network Formation and Lithography

Christopher Barner‐Kowollik, Jan Hobich, Hatice Mutlu, Eva Blasco et al.
Angewandte Chemie
Photochromic and Fluorescence Chemistry
article

Synergistic Two‐Color Photochemical Polymer Network Formation and Lithography

Christopher Barner‐Kowollik, Jan Hobich, Hatice Mutlu, Eva Blasco, Florian A. Feist, Paul Somers, Xingyu Wu, Willie Scheibel, Natalia Herdt
article en

Abstract

Abstract We introduce synergistic two‐color lithography as an advanced wavelength‐gated strategy for spatially and temporally controlling polymer network formation. Our photoresist entails two photoswitches, i.e., diarylindenone epoxide (DIO) and strained azobenzene (SA), each activated at a judiciously selected wavelength, i.e., 375 or 430 nm. Under specific conditions of photon flux, simultaneous irradiation at both wavelengths induces a (3 + 2) cycloaddition between the photoactivated DIO′ and SA′ species, generating covalently crosslinked networks, whereas under these specifically determined conditions, single‐wavelength exposure does not induce solidification. Kinetic analysis highlights the potential of synergistic activation to enable advanced additive manufacturing. We implemented the two‐color activated covalent bond forming system in a dual‐laser lithographic platform enabling the fabrication of well‐defined structures, including segmented ring and butterfly architectures by simply activating and deactivating one of the colors of light.

Angewandte ChemieVol. 137(48)
Karlsruhe Institute of Technology (DE), University of Kaiserslautern (DE), Queensland University of Technology (AU), Heidelberg University (DE), Institut für Polymerwerkstoffe (DE), Leibniz-Institut für Verbundwerkstoffe GmbH (DE)
Openalex Percentile: Top 79%
Photochromic and Fluorescence Chemistry
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