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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=96497"><dc:title>High-porosity conjugated polyelectrolytes synthesized via Sonogashira–Hagihara coupling in concentrated emulsions</dc:title><dc:creator>Markovič,	Aleksander Saša	(Avtor)
	</dc:creator><dc:creator>Lievens,	Siebe	(Avtor)
	</dc:creator><dc:creator>Hanozin,	Emeline	(Avtor)
	</dc:creator><dc:creator>Velimirovic,	Milica	(Avtor)
	</dc:creator><dc:creator>Pintar,	Albin	(Avtor)
	</dc:creator><dc:creator>Kovačič,	Sebastijan	(Avtor)
	</dc:creator><dc:subject>adsorption</dc:subject><dc:subject>degradation</dc:subject><dc:subject>hydrogels</dc:subject><dc:subject>oxides</dc:subject><dc:subject>polymers</dc:subject><dc:description>Conjugated polyelectrolyte (CPE) hydrogels uniquely combine π-conjugation, ionic functionality, and water compatibility in a single-polymer network. This work reports on the design, synthesis, and application of high-porosity CPE hydrogels obtained via the Sonogashira–Hagihara cross-coupling reaction as a polymerization chemistry in a high internal phase emulsion (HIPE) template. In this way, we combine the hydrophilic and π-conjugated electronic properties of CPEs with the high porosity of polymerized high internal phase emulsions (polyHIPEs or PHs), enabling the development of a multifunctional polymer platform. High-porosity CPE-PHs exhibit a surface area of up to 355 m2·g–1, excellent water uptakes of up to ∼25 g·g–1, and visible-light absorption with band edges at 720 and 610 nm and band gaps of 2.35 and 2.47 eV for anionic CPE-PH–SO3̅ and cationic CPE-PH-NMe3+, respectively. These CPE-PHs are then used to remove the endocrine-disrupting chemical bisphenol A (BPA) as a model water pollutant. The CPE-PH–SO3̅ demonstrates exceptional performance, achieving overall removal efficiencies of 93% and 96% through synergistic adsorption (∼71% and ∼50%, respectively) and visible light-driven photocatalysis (∼22% and ∼46%, respectively) during 8 and 24 h experiments. These efficiencies are among the highest reported for organic photocatalyst. In contrast, the cationic analogue CPE-PH-NMe3+ suffers from oxidative degradation and thus limited activity. Stability studies confirmed that CPE-PH–SO3̅ retains its structural and electronic integrity during prolonged operation. These results demonstrate the potential of high-porosity CPE-PH hydrogels as a multifunctional polymer platform that synergistically integrates adsorption and heterogeneous photocatalysis for robust and efficient water applications.</dc:description><dc:publisher>ACS Publications</dc:publisher><dc:date>2026</dc:date><dc:date>2026-01-14 14:18:11</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>96497</dc:identifier><dc:language>sl</dc:language><dc:rights>© 2026 The Authors.</dc:rights></rdf:Description></rdf:RDF>
