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Anthracene-Based Thiol–Ene Networks with Thermo-Degradable and Photo-Reversible Properties
Author(s) -
Jonas Van Damme,
Otto van den Berg,
Joost Brancart,
Laetitia Vlaminck,
C. Lee Huyck,
Guy Van Assche,
Bruno Van Mele,
Filip Du Prez
Publication year - 2017
Publication title -
macromolecules
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.994
H-Index - 313
eISSN - 1520-5835
pISSN - 0024-9297
DOI - 10.1021/acs.macromol.6b02400
Subject(s) - differential scanning calorimetry , anthracene , dimer , monomer , alkene , materials science , polymer chemistry , rheology , photopolymer , chemistry , polymer , photochemistry , organic chemistry , composite material , thermodynamics , physics , catalysis
Reversible networks based on an alkene-functionalized dimer of 9-anthracenemethanol were synthesized by photoinitiated radical thiol–ene polyaddition, using either a poly(dimethylsiloxane-co-propylmercaptomethylsiloxane) or a novel aliphatic trithiol synthesized from 1,2,4-trivinylcyclohexane in a simple two-step procedure. The obtained networks were analyzed using differential scanning calorimetry, dynamic mechanical analysis, polarization microscopy, X-ray diffraction, and (photo)rheology. The two types of networks showed weak endothermic transitions between 50 and 60 °C, which proved to originate either from melting of a crystalline anthracene-dimer phase (trithiol network) or from a liquid crystalline phase (PDMS network) based on X-ray diffraction and polarization microscopy. Using rheology, both types of networks were shown to cleanly decompose into multifunctional anthracene monomers at temperatures above 180 °C. Irradiation of these anthracene monomers resulted in the formation of networks having ...

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