Monocomponent Photoinitiators based on Benzophenone-Carbazole Structure for LED Photoinitiating Systems and Application on 3D Printing.

3D printing benzophenone carbazole monocomponent photoinitiator

Journal

Polymers
ISSN: 2073-4360
Titre abrégé: Polymers (Basel)
Pays: Switzerland
ID NLM: 101545357

Informations de publication

Date de publication:
22 Jun 2020
Historique:
received: 10 06 2020
revised: 18 06 2020
accepted: 19 06 2020
entrez: 26 6 2020
pubmed: 26 6 2020
medline: 26 6 2020
Statut: epublish

Résumé

In this article, different substituents (benzoyl, acetyl, styryl) are introduced onto the carbazole scaffold to obtain 8 novel carbazole derivatives. Interestingly, a benzoyl substituent, connected to a carbazole group, could form a benzophenone moiety, which composes a monocomponent Type II benzophenone-carbazole photoinitiator (PI). The synergetic effect of the benzophenone moiety and the amine in the carbazole moiety is expected to produce high performance photoinitiating systems (PISs) for the free radical photopolymerization (FRP). For different substituents, clear effects on the light absorption properties are demonstrated using UV-Visible absorption spectroscopy. Benzophenone-carbazole PIs can initiate the FRP of acrylates alone (monocomponent Type II photoinitiator behavior). In addition, fast polymerization rates and high function conversions of acrylate are observed when an amine and/or an iodonium salt are added in systems. Benzophenone-carbazole PIs have good efficiencies in cationic photopolymerization (CP) upon LED @ 365 nm irradiation in the presence of iodonium salt. In contrast, other PIs without synergetic effect demonstrate unsatisfied photopolymerization profiles in the same conditions. The best PIS identified for the free radical photopolymerization were used in three-dimensional (3D) printing. Steady state photolysis and fluorescence quenching experiments were carried out to investigate the reactivity and the photochemistry and photophysical properties of PIs. The free radicals, generated from the studied PISs, are detected by the electron spin resonance - spin trapping technique. The proposed chemical mechanisms are provided and the structure/reactivity/efficiency relationships are also discussed. All the results showed that the benzophenone-carbazole PIs have a good application potential, and this work provides a rational design route for PI molecules. Remarkably, BPC2-BPC4, C6, C8 were never synthetized before; therefore, 5 of the 8 compounds are completely new.

Identifiants

pubmed: 32580350
pii: polym12061394
doi: 10.3390/polym12061394
pmc: PMC7362224
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : China Scholarship Council
ID : CSC201906880009

Références

Acc Chem Res. 2016 Sep 20;49(9):1980-9
pubmed: 27560545
Langmuir. 2004 Nov 9;20(23):10020-9
pubmed: 15518489
Macromol Rapid Commun. 2016 May;37(10):840-4
pubmed: 27072016
Adv Mater. 2018 Oct;30(41):e1706344
pubmed: 29756242
Polymers (Basel). 2020 Jun 22;12(6):
pubmed: 32580350
Chem Rev. 2016 Sep 14;116(17):10212-75
pubmed: 26745441
Angew Chem Int Ed Engl. 2019 Mar 22;58(13):4400-4404
pubmed: 30666770
Photochem Photobiol Sci. 2012 Aug;11(8):1377-82
pubmed: 22711007
J Polym Sci A Polym Chem. 2009 Mar 1;47(5):1429-1439
pubmed: 20161099

Auteurs

Shaohui Liu (S)

Université de Haute-Alsace, CNRS, IS2M UMR 7361, F-68100 Mulhouse, France.
Université de Strasbourg, Grand Est, 67200 Strasbourg, France.

Hong Chen (H)

Université de Haute-Alsace, CNRS, IS2M UMR 7361, F-68100 Mulhouse, France.
Université de Strasbourg, Grand Est, 67200 Strasbourg, France.

Yijun Zhang (Y)

Université de Haute-Alsace, CNRS, IS2M UMR 7361, F-68100 Mulhouse, France.
Université de Strasbourg, Grand Est, 67200 Strasbourg, France.

Ke Sun (K)

Université de Haute-Alsace, CNRS, IS2M UMR 7361, F-68100 Mulhouse, France.
Université de Strasbourg, Grand Est, 67200 Strasbourg, France.

Yangyang Xu (Y)

Université de Haute-Alsace, CNRS, IS2M UMR 7361, F-68100 Mulhouse, France.
Université de Strasbourg, Grand Est, 67200 Strasbourg, France.

Fabrice Morlet-Savary (F)

Université de Haute-Alsace, CNRS, IS2M UMR 7361, F-68100 Mulhouse, France.
Université de Strasbourg, Grand Est, 67200 Strasbourg, France.

Bernadette Graff (B)

Université de Haute-Alsace, CNRS, IS2M UMR 7361, F-68100 Mulhouse, France.
Université de Strasbourg, Grand Est, 67200 Strasbourg, France.

Guillaume Noirbent (G)

Aix Marseille Univ, CNRS, ICR UMR 7273, F-13397 Marseille, France.

Corentin Pigot (C)

Aix Marseille Univ, CNRS, ICR UMR 7273, F-13397 Marseille, France.

Damien Brunel (D)

Aix Marseille Univ, CNRS, ICR UMR 7273, F-13397 Marseille, France.

Malek Nechab (M)

Aix Marseille Univ, CNRS, ICR UMR 7273, F-13397 Marseille, France.

Didier Gigmes (D)

Aix Marseille Univ, CNRS, ICR UMR 7273, F-13397 Marseille, France.

Pu Xiao (P)

Research School of Chemistry, Australian National University, Canberra, ACT 2601, Australia.

Frédéric Dumur (F)

Aix Marseille Univ, CNRS, ICR UMR 7273, F-13397 Marseille, France.

Jacques Lalevée (J)

Université de Haute-Alsace, CNRS, IS2M UMR 7361, F-68100 Mulhouse, France.
Université de Strasbourg, Grand Est, 67200 Strasbourg, France.

Classifications MeSH