As a new example of intrinsically water-triggered phenomena, we report underwater dehydration of the statistical copolymers synthesized from triethanolamine borate (TEAB) methacrylate and styrene (St) induced by the hydrolysis of the pendant TEAB group. TEAB possesses high polarity owing to its internal Lewis adduct structure, which is lost by hydrolysis to triethanolamine (TEA) with a lower dipole moment. Therefore, the hydration of the copolymers became unfavorable through the hydrolysis of the pendant TEAB to TEA, despite polyol formation, and through a hydrophobic interaction based on St moieties becoming alternatively dominant. The dehydration behavior of the copolymers, along with the hydrolysis of the pendant TEAB group, was systematically investigated. The water solubility of the copolymers was found to be dependent on the gradient of the hydrolysis equilibrium of TEAB on the side chains and was the lowest for the TEA state. These findings offer a novel concept toward designing water-responsive materials.
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http://dx.doi.org/10.1021/acsmacrolett.2c00161 | DOI Listing |
Food Addit Contam Part A Chem Anal Control Expo Risk Assess
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Center for Food Safety and Applied Nutrition, United States Food and Drug Administration, College Park, MD, USA.
Fluorotelomer-based acrylate polymers and surfactants used to grease-proof food contact paper (FCP) are potential sources of dietary exposure to perfluoroalkyl substances (PFAS). Food contact substances (FCS) containing polyfluorinated long-chains (≥C8) were voluntarily removed by their manufacturers from the U.S.
View Article and Find Full Text PDFACS Macro Lett
November 2024
Center for Multidimensional Carbon Materials (CMCM), Institute for Basic Science (IBS), Ulsan 44919, Republic of Korea.
A series of -7-thiabicyclo[2.2.1]hept-5-ene-2,3-dicarboximides were synthesized and polymerized using Schrock's catalyst, 2,6-diisopropylphenylimidoneophylidene molybdenum(VI) bis(hexafluoro--butoxide).
View Article and Find Full Text PDFBiomacromolecules
October 2024
Institute for Bioscience and Biotechnology Research, University of Maryland, Rockville, Maryland 20850, United States.
Zwitterionic polymers, ampholytic macromolecules containing ionic moieties of opposite sign on the same pendant groups, exhibit strong protein-repulsive properties and an inherent biological inertness. For that reason, these highly hydrated inner salt macromolecules have emerged as some of the most viable alternatives to poly(ethylene glycol) (PEG), a gold standard in enabling stealth behavior in life science applications. However, the structural diversity of polymer zwitterions remains limited, and currently available macromolecules do not possess an intrinsic ability to undergo hydrolytical degradation, an important prerequisite for use in drug delivery applications.
View Article and Find Full Text PDFACS Macro Lett
July 2024
Faculty of Materials Science and Engineering, South China University of Technology, Guangzhou 510640, China.
Silyl ether constitutes a multipurpose (macro)molecular functionality for being, e.g., SuFEx-clickable and easily cleavable as a hydroxyl precursor.
View Article and Find Full Text PDFJ Am Chem Soc
May 2024
Department of Chemistry, Yonsei University, Seoul 03722, Republic of Korea.
Hydrogels hold significant promise as drug delivery systems due to their distinct advantage of sustained localized drug release. However, the challenge of regulating the initial burst release while achieving precise control over degradation and drug-release kinetics persists. Herein, we present an ABA-type triblock copolymer-based hydrogel system with precisely programmable degradation and release kinetics.
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