Abstract

A series of eleven push–pull chromophores with specific structures have been designed for the free radical polymerization of acrylates, but also for the fabrication of photocomposites and 3D-printed structures. New photoinitiating systems comprising the different push–pull dyes showed excellent photochemical reactivities at 405 nm. Notably, polymerization reactions could be initiated with light-emitting diodes (LEDs) which constitute a unique opportunity to promote the free radical polymerization under mild conditions, i.e., low light intensity (e.g., sunlight) and under air. Photopolymerization is an active research field, and push–pull dyes have already been investigated for this purpose. Besides, it remains of crucial interest to investigate new reactive structures capable of efficiently initiating photopolymerization reactions. The plausible potential of these structures to act as efficient photoinitiators in vat photopolymerization (or 3D printing) and fabrication of photocomposites prompts us to select eleven new push–pull dyes to design multi-component photoinitiating systems activable with LEDs emitting at 405 nm. Precisely, a tertiary amine, i.e., ethyl dimethylaminobenzoate (EDB) used as an electron/hydrogen donor and an iodonium salt used as an electron acceptor were selected to behave as powerful co-initiators to construct three-component photoinitiating systems (PISs) with the different push–pull dyes. Among these new PISs, dye 8 and 9-based PISs could efficiently promote the free radical photopolymerization of acrylates upon exposure to a LED emitting at 405 nm also upon sunlight irradiation, highlighting their huge performance. Photoinitiating abilities could be explained on the basis of steady state photolysis experiments. Fluorescence measurements and electron spin resonance (ESR) spin-trapping experiments were also performed to obtain a deeper insight into the chemical mechanisms supporting the polymerization reaction and determine the way the initiating species, i.e., the radicals, are observed. Finally, two investigated dye-based PISs were applied to the fabrications of photocomposites. Three-dimensional patterns with excellent spatial resolutions were generated by the laser writing technique to identify the effects of photopolymerization of acrylates both in the absence and presence of fillers (silica). Interestingly, comparison between the 3D objects fabricated by the PISs/monomer systems and the PISs/monomer/filler photocomposites indicates that the newly designed photocomposites are suitable for practical applications.

Highlights

  • Push–pull dyes composed of a donor and an acceptor connected by mean of a conjugated spacer have been the focus of intense research efforts due to the wide range of applications in which these dyes can find applications [1,2,3,4,5]

  • With aim at developing push–pull dyes with high molar extinction coefficients and broad absorption spectra extending over the visible range, two synthetic approaches were employed

  • Photoinitiating systems used in this work are composed of a dye, iodonium salt (Iod) and the amine (EDB) and are exposed to an light-emitting diodes (LEDs)@405 nm (I0 = 110 mW cm−2 ) in ambient conditions and under air

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Summary

Introduction

Push–pull dyes composed of a donor and an acceptor connected by mean of a conjugated spacer have been the focus of intense research efforts due to the wide range of applications in which these dyes can find applications [1,2,3,4,5]. By finely tuning both the electron-donating and electron-accepting abilities of the two partners as well as on the length of the spacer, the molar extinction coefficients and the position of the ICT band can be carefully controlled [2] Benefiting from these different advantages (high molar extinction coefficient, absorption in the visible range), push–pull dyes have been identified as promising candidates for the design of visible light photoinitiators activable under low-light intensity [25,26,27,28]. The design of highly reactive dyes capable of initiating photopolymerization processes under light emitted by 405 nm LEDs are still scarcely available in the literature, and a great deal of efforts remains to be carried out in order to develop photoinitiators operating under very low-light intensities [29,30,31,32,33] Such a goal can only be achieved by chemical engineering. Aiming at improving the knowledge of photopolymerization, the fabrication of novel useful photocomposites by use of push–pull dyes as photoinitiators and in the presence of fillers was considered by our group as one of the various useful applications which is only scarcely reported in the literature [36]

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