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<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/"><rdf:Description rdf:about="https://dk.um.si/IzpisGradiva.php?id=94207"><dc:title>Myrcene-based porous polymers via emulsion templating and thiol-ene polymerization</dc:title><dc:creator>Koler,	Amadeja	(Avtor)
	</dc:creator><dc:creator>Krajnc,	Peter	(Avtor)
	</dc:creator><dc:subject>photochemistry</dc:subject><dc:subject>terpenes</dc:subject><dc:subject>thiol-ene reaction</dc:subject><dc:subject>polyHIPEs</dc:subject><dc:subject>myrcene</dc:subject><dc:description>Porous polymer networks were synthesized via thiol-ene photo-polymerization using a naturally occurring terpene, myrcene and the multifunctional thiol, trimethylolpropane tris(3-mercaptopropionate). A highly porous structure (up to 80% porosity) was achieved by polymerizing the monomeric phase of high internal phase emulsions (HIPEs), composed of myrcene and trimethylolpropane tris(3-mercaptopropionate) in the presence of ethylene glycol dimethacrylate, which facilitated the formation of polyHIPE materials. Myrcene was incorporated in concentrations ranging from 9 to 40 mol%, and its content was found to significantly influence the resulting polymer morphology. Depending on the formulation, both bicontinuous-like and open-cell polyHIPE morphologies were obtained. In addition to myrcene content, the thiol-to-alkene functional group ratio (1:1 ratio of thiol to alkene groups, as well as formulations with an excess of alkene functionalities relative to thiols).</dc:description><dc:publisher>Springer</dc:publisher><dc:date>2025</dc:date><dc:date>2025-08-08 10:40:02</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>94207</dc:identifier><dc:language>sl</dc:language><dc:rights>© The Author(s) 2025
</dc:rights></rdf:Description></rdf:RDF>
