Free Radical Photopolymerization and 3D Printing Using Newly Developed Dyes: Indane-1,3-Dione and 1<i>H</i>-Cyclopentanaphthalene-1,3-Dione Derivatives as Photoinitiators in Three-Component Systems
The design of photoinitiating systems with excellent photochemical reactivities at 405nm LED is one of the obstacles to efficiently promote free radical polymerization in mild conditions (e.g., low light intensity, under air). Here, our actual search for new multicomponent photoinitiating systems at...
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doaj-c62c22b3661e4c55b0808dd810b5adf82020-11-25T02:04:46ZengMDPI AGCatalysts2073-43442020-04-011046346310.3390/catal10040463Free Radical Photopolymerization and 3D Printing Using Newly Developed Dyes: Indane-1,3-Dione and 1<i>H</i>-Cyclopentanaphthalene-1,3-Dione Derivatives as Photoinitiators in Three-Component SystemsKe Sun0Corentin Pigot1Hong Chen2Malek Nechab3Didier Gigmes4Fabrice Morlet-Savary5Bernadette Graff6Shaohui Liu7Pu Xiao8Frédéric Dumur9Jacques Lalevée10Université de Haute-Alsace, CNRS, IS2M UMR 7361, F-68100 Mulhouse, FranceAix Marseille Université, CNRS, ICR UMR 7273, F-13397 Marseille, FranceUniversité de Haute-Alsace, CNRS, IS2M UMR 7361, F-68100 Mulhouse, FranceAix Marseille Université, CNRS, ICR UMR 7273, F-13397 Marseille, FranceAix Marseille Université, CNRS, ICR UMR 7273, F-13397 Marseille, FranceUniversité de Haute-Alsace, CNRS, IS2M UMR 7361, F-68100 Mulhouse, FranceUniversité de Haute-Alsace, CNRS, IS2M UMR 7361, F-68100 Mulhouse, FranceUniversité de Haute-Alsace, CNRS, IS2M UMR 7361, F-68100 Mulhouse, FranceResearch School of Chemistry, Australian National University, Canberra ACT 2601, AustraliaAix Marseille Université, CNRS, ICR UMR 7273, F-13397 Marseille, FranceUniversité de Haute-Alsace, CNRS, IS2M UMR 7361, F-68100 Mulhouse, FranceThe design of photoinitiating systems with excellent photochemical reactivities at 405nm LED is one of the obstacles to efficiently promote free radical polymerization in mild conditions (e.g., low light intensity, under air). Here, our actual search for new multicomponent photoinitiating systems at 405nm LED prompts us to develop new dyes based on push–pull structures. In the present paper, we chose two series of new dyes which possess indane-1,3-dione and 1<i>H</i>-cyclopenta naphthalene-1,3-dione groups as the electron-withdrawing groups, since they have the great potential to behave as sensitive and remarkable photoinitiators in vat photopolymerization/3D printing. When incorporated with a tertiary amine (ethyl dimethylaminobenzoate EDB, used as electron/hydrogen donor) and an iodonium salt (used as electron acceptor) as the three-component photoinitiating systems (PISs), and among a series of 21 dyes, 10 of them could efficiently promote the free radical photopolymerization of acrylates. Interestingly, steady state photolysis experiments revealed different behaviors of the dyes. Fluorescence experiments and free energy change calculations for redox processes were also carried out to investigate the relevant chemical mechanisms. Additionally, the formation of radicals from the investigated PISs was clearly observed by electron spin resonance (ESR) spin-trapping experiments. Finally, stereoscopic 3D patterns were successfully fabricated by the laser writing technique. In this work, the use of push–pull dyes based on the naphthalene scaffold as photoinitiators of polymerization is reported for the first time in a systematic study aiming at investigating the structure–performance relationship for irradiation carried out at 405 nm. By carefully selecting the electron donors used in the two series of push–pull dyes, novel and high-performance photoinitiating systems operating at 405 nm are thus proposed.https://www.mdpi.com/2073-4344/10/4/463push–pull dyefree radical polymerizationthree-component systemLED3D printing |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ke Sun Corentin Pigot Hong Chen Malek Nechab Didier Gigmes Fabrice Morlet-Savary Bernadette Graff Shaohui Liu Pu Xiao Frédéric Dumur Jacques Lalevée |
spellingShingle |
Ke Sun Corentin Pigot Hong Chen Malek Nechab Didier Gigmes Fabrice Morlet-Savary Bernadette Graff Shaohui Liu Pu Xiao Frédéric Dumur Jacques Lalevée Free Radical Photopolymerization and 3D Printing Using Newly Developed Dyes: Indane-1,3-Dione and 1<i>H</i>-Cyclopentanaphthalene-1,3-Dione Derivatives as Photoinitiators in Three-Component Systems Catalysts push–pull dye free radical polymerization three-component system LED 3D printing |
author_facet |
Ke Sun Corentin Pigot Hong Chen Malek Nechab Didier Gigmes Fabrice Morlet-Savary Bernadette Graff Shaohui Liu Pu Xiao Frédéric Dumur Jacques Lalevée |
author_sort |
Ke Sun |
title |
Free Radical Photopolymerization and 3D Printing Using Newly Developed Dyes: Indane-1,3-Dione and 1<i>H</i>-Cyclopentanaphthalene-1,3-Dione Derivatives as Photoinitiators in Three-Component Systems |
title_short |
Free Radical Photopolymerization and 3D Printing Using Newly Developed Dyes: Indane-1,3-Dione and 1<i>H</i>-Cyclopentanaphthalene-1,3-Dione Derivatives as Photoinitiators in Three-Component Systems |
title_full |
Free Radical Photopolymerization and 3D Printing Using Newly Developed Dyes: Indane-1,3-Dione and 1<i>H</i>-Cyclopentanaphthalene-1,3-Dione Derivatives as Photoinitiators in Three-Component Systems |
title_fullStr |
Free Radical Photopolymerization and 3D Printing Using Newly Developed Dyes: Indane-1,3-Dione and 1<i>H</i>-Cyclopentanaphthalene-1,3-Dione Derivatives as Photoinitiators in Three-Component Systems |
title_full_unstemmed |
Free Radical Photopolymerization and 3D Printing Using Newly Developed Dyes: Indane-1,3-Dione and 1<i>H</i>-Cyclopentanaphthalene-1,3-Dione Derivatives as Photoinitiators in Three-Component Systems |
title_sort |
free radical photopolymerization and 3d printing using newly developed dyes: indane-1,3-dione and 1<i>h</i>-cyclopentanaphthalene-1,3-dione derivatives as photoinitiators in three-component systems |
publisher |
MDPI AG |
series |
Catalysts |
issn |
2073-4344 |
publishDate |
2020-04-01 |
description |
The design of photoinitiating systems with excellent photochemical reactivities at 405nm LED is one of the obstacles to efficiently promote free radical polymerization in mild conditions (e.g., low light intensity, under air). Here, our actual search for new multicomponent photoinitiating systems at 405nm LED prompts us to develop new dyes based on push–pull structures. In the present paper, we chose two series of new dyes which possess indane-1,3-dione and 1<i>H</i>-cyclopenta naphthalene-1,3-dione groups as the electron-withdrawing groups, since they have the great potential to behave as sensitive and remarkable photoinitiators in vat photopolymerization/3D printing. When incorporated with a tertiary amine (ethyl dimethylaminobenzoate EDB, used as electron/hydrogen donor) and an iodonium salt (used as electron acceptor) as the three-component photoinitiating systems (PISs), and among a series of 21 dyes, 10 of them could efficiently promote the free radical photopolymerization of acrylates. Interestingly, steady state photolysis experiments revealed different behaviors of the dyes. Fluorescence experiments and free energy change calculations for redox processes were also carried out to investigate the relevant chemical mechanisms. Additionally, the formation of radicals from the investigated PISs was clearly observed by electron spin resonance (ESR) spin-trapping experiments. Finally, stereoscopic 3D patterns were successfully fabricated by the laser writing technique. In this work, the use of push–pull dyes based on the naphthalene scaffold as photoinitiators of polymerization is reported for the first time in a systematic study aiming at investigating the structure–performance relationship for irradiation carried out at 405 nm. By carefully selecting the electron donors used in the two series of push–pull dyes, novel and high-performance photoinitiating systems operating at 405 nm are thus proposed. |
topic |
push–pull dye free radical polymerization three-component system LED 3D printing |
url |
https://www.mdpi.com/2073-4344/10/4/463 |
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