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      Bis-chalcone derivatives derived from natural products as near-UV/visible light sensitive photoinitiators for 3D/4D printing

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          Abstract

          Four series of novel bis-chalcone compounds with excellent performances have been synthesized and examined for the first time as photoinitiators in combination with an amine and an iodonium salt for the FRP of acrylates and the CP of EPOX.

          Abstract

          Four series of bis-chalcone compounds based on benzylpiperidinone, tetrahydrothiopyranone, pyridine or biphenyl central parts are designed and synthesized, enabling the development of ten bis-chalcones varying both by the central cores and by the substitution patterns ( ortho, meta, para-positions) and the choice of the different groups attached to the peripheral substituents (alkoxy or allyloxy-substituted aromatic rings, thiophene, or ferrocene). In this series of ten bis-chalcones, eight of them were never synthesized before ( i.e. only bis-chalcones 8 and 10 were already reported albeit never used as photoinitiators). These different dyes are proposed as new near-UV/visible light sensitive photoinitiators, in combination with an amine and an iodonium salt, to initiate the free radical photopolymerization (FRP) of PEG-diacrylate and the cationic photopolymerization (CP) of EPOX under LED@405 nm and LED@375 nm irradiation conditions. For the photopolymerization of acrylates carried out between thin films in laminate, all the bis-chalcones proposed in this work show higher photoinitiation abilities upon irradiation with a LED at 375 nm than at 405 nm, which is mainly due to their excellent light absorption properties in the near-UV region. Markedly, in contrast with the other two series of bis-chalcone compounds, pyridine-based bis-chalcones prove to be the most efficient photoinitiators, especially the bis-chalcones 5 and 9. Furthermore, all of them can also promote the cationic polymerization of epoxides upon LED irradiation at 375 nm, in the presence of an iodonium salt and an amine. More interestingly, some 3D patterns fabricated through the free radical polymerization of PEG-diacrylate demonstrate reversible swelling properties and shape-memory for access to 4D printing.

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          Shape-Memory Polymers

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            Biodegradable, elastic shape-memory polymers for potential biomedical applications.

            The introduction of biodegradable implant materials as well as minimally invasive surgical procedures in medicine has substantially improved health care within the past few decades. This report describes a group of degradable thermoplastic polymers that are able to change their shape after an increase in temperature. Their shape-memory capability enables bulky implants to be placed in the body through small incisions or to perform complex mechanical deformations automatically. A smart degradable suture was created to illustrate the potential of these shape-memory thermoplastics in biomedical applications.
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              Recent advances in shape memory polymers and composites: a review

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                Author and article information

                Contributors
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                Journal
                MCFAC5
                Materials Chemistry Frontiers
                Mater. Chem. Front.
                Royal Society of Chemistry (RSC)
                2052-1537
                January 25 2021
                2021
                : 5
                : 2
                : 901-916
                Affiliations
                [1 ]Université de Haute-Alsace, CNRS, IS2M UMR 7361
                [2 ]F-68100 Mulhouse
                [3 ]France
                [4 ]Université de Strasbourg
                [5 ]Aix Marseille Univ, CNRS, ICR UMR 7273
                [6 ]F-13397 Marseille
                [7 ]Research School of Chemistry, Australian National University
                [8 ]Camberra
                [9 ]Australia
                Article
                10.1039/D0QM00755B
                34360195-9508-44ed-95e0-3aa1e42cb293
                © 2021

                http://rsc.li/journals-terms-of-use

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