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Merocyanine photoacids (MCHs) have found applications in chemical, material, energy, and biomedical areas, and are currently being investigated for industrial applications. Hydrolysis, relatively high dark acidity, and moderate solubility in water are the major concerns for their practical applications. Inspired by the structure of the cell membrane, we incorporated the most commonly used MCH into sodium dodecyl sulfate (SDS) micelles. NMR and UV-vis absorption studies indicated that the MCH was located near the surface of the micelle with the positively charged indolinium moiety in the micelle and the neutral phenol moiety exposed to water. The location allows the MCH to be protected by SDS while still being able to release protons to the aqueous solution. In the presence of 15 mM of SDS, the half-life of the MCH in aqueous solutions increased over a hundred times to nearly half a year. In addition, the solubility increased by several orders of magnitude and the dark acidity decreased, which significantly enhances its capability of photo pH-modulation. Structure modification with a dodecoxyl group, together with the addition of SDS, essentially stopped the hydrolysis.
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http://dx.doi.org/10.1021/acs.jpcb.5c04723 | DOI Listing |
J Phys Chem B
September 2025
Department of Chemistry and Chemical Engineering, Florida Institute of Technology, Melbourne, Florida 32901, United States.
Merocyanine photoacids (MCHs) have found applications in chemical, material, energy, and biomedical areas, and are currently being investigated for industrial applications. Hydrolysis, relatively high dark acidity, and moderate solubility in water are the major concerns for their practical applications. Inspired by the structure of the cell membrane, we incorporated the most commonly used MCH into sodium dodecyl sulfate (SDS) micelles.
View Article and Find Full Text PDFAdv Mater
July 2025
State Key Laboratory of Precision and Intelligent Chemistry, University of Science and Technology of China, Hefei, Anhui, 230026, China.
Photomanipulation of the environmental pH plays a crucial role in modulating the reaction kinetics and engineering material functionalities. While conventional merocyanine photoacids offer pH modulability, their practical implementation is fundamentally constrained by aqueous dissolution and laborious regeneration. Here, a transformative strategy is reported through the covalent integration of merocyanine photoacids into hydrophilic polymer networks to construct regenerative photoacid matrices, which stably retain protons in the dark and spatiotemporally liberate them upon illumination.
View Article and Find Full Text PDFJ Phys Chem A
June 2025
University of Southern California, Los Angeles, California 90007, United States.
Water structure and proton dynamics in complex environments, such as mixed electrolytes, biological environments, and microdroplet surfaces, are often hypothesized to affect reaction thermodynamics, kinetics, and selectivity. Toward better understanding the influence of water microphases in complex mixtures, this study leverages the proton-dependent recovery kinetics of a merocyanine photoacid in acetonitrile (ACN) and dimethyl sulfoxide (DMSO) over a range of water mole fractions χ. We report that the rates of recovery, , do not scale linearly with χ.
View Article and Find Full Text PDFChem Commun (Camb)
April 2025
Institute of Organic Chemistry, Faculty of Chemistry and Pharmacy, University of Regensburg, Universitätsstraße 31, 93053 Regensburg, Germany.
Visible light-driven proton transfer is crucial in nature and catalysis. Here, we report that protic merocyanine-based photoswitches act as efficient and recyclable homogeneous Brønsted acid catalysts under blue or green light irradiation. Photo-promoted proton release efficiently enables Friedel-Crafts reactions with easy catalyst recovery and reuse.
View Article and Find Full Text PDFJACS Au
November 2024
School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240, P. R. China.
Precision synthesis of polyorganosiloxanes and temporal control over the polymerization process during ring-opening polymerization (ROP) of cyclosiloxanes remain challenging due to the occurrence of side reactions, e.g., intramolecular transfer (backbiting) and intermolecular chain transfer, and irreversible catalyst transformation.
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