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含吡啶鎓盐的电荷转移络合物(CTCs):迈向高效双光化学/热引发剂及3D打印应用

Charge Transfer Complexes (CTCs) with Pyridinium Salts: Toward Efficient Dual Photochemical/Thermal Initiators and 3D Printing Applications.

作者信息

Ma Qiang, Buchon Loïc, Magné Valentin, Graff Bernadette, Morlet-Savary Fabrice, Xu Yangyang, Benltifa Mahmoud, Lakhdar Sami, Lalevée Jacques

机构信息

CNRS, Université de Haute-Alsace, IS2M UMR 7361, Mulhouse, F-68100, France.

Université de Strasbourg, Strasbourg, F-67081, France.

出版信息

Macromol Rapid Commun. 2022 Oct;43(19):e2200314. doi: 10.1002/marc.202200314. Epub 2022 May 15.

DOI:10.1002/marc.202200314
PMID:35526219
Abstract

In both organic and polymer synthesis, photochemistry of charge transfer complexes (CTCs) is considered as a powerful approach to expand visible-light-driven radical chemistry reaction. One reports herein on the development of a class of useful CTCs using pyridinium salts as efficient electron acceptors (combined with N, N, 3,5-tetramethylaniline, TMA) to achieve a multiwavelength (375-560 nm) metal-free LED photopolymerization process under mild conditions (open to air, without monomer purification and inhibitor removal). The UV-vis absorption spectra and molecular modeling simultaneously verify its potential blue-green absorbing wavelength range. Also, their good thermal initiation behavior at relatively low temperatures makes it easier to achieve thick samples and/or polymerization in the shadow region in practice. More importantly, with excellent photoinitiating capability, the formulation is successfully applied to direct laser write (DLW) and high-resolution 3D printing, yielding a series of objects with well-defined structures, such as letters, ring, solid squares, and chess pieces. These new pyridinium salt acceptors further extend the applicability to visible photopolymerizable resins and additive-containing formulations for efficient surface and deep curing.

摘要

在有机合成和聚合物合成中,电荷转移络合物(CTCs)的光化学被视为扩展可见光驱动自由基化学反应的一种强大方法。本文报道了一类有用的CTCs的开发,该CTCs使用吡啶鎓盐作为有效的电子受体(与N,N,3,5-四甲基苯胺,TMA结合),以在温和条件下(暴露于空气中,无需单体纯化和去除抑制剂)实现多波长(375-560nm)无金属LED光聚合过程。紫外-可见吸收光谱和分子建模同时验证了其潜在的蓝绿色吸收波长范围。此外,它们在相对较低温度下良好的热引发行为使得在实际中更容易获得厚样品和/或在阴影区域进行聚合。更重要的是,凭借出色的光引发能力,该配方成功应用于直接激光写入(DLW)和高分辨率3D打印,生成了一系列结构明确的物体,如字母、戒指、实心方块和棋子。这些新型吡啶鎓盐受体进一步扩展了对可见光可光聚合树脂和含添加剂配方的适用性,以实现高效的表面和深层固化。

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