We report the design and synthesis of a nano-container consisting of mesoporous silica nanoparticles with the pore openings covered by "snap-top" caps that are opened by near-IR light. A photo transducer molecule that is a reducing agent in an excited electronic state is covalently attached to the system. Near IR two-photon excitation causes inter-molecular electron transfer that reduces a disulfide bond holding the cap in place, thus allowing the cargo molecules to escape. We describe the operation of the "snap-top" release mechanism by both one- and two-photon activation. This system presents a proof of concept of a near-IR photoredox-induced nanoparticle delivery system that may lead to a new type of photodynamic drug release therapy.
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http://dx.doi.org/10.1039/c3nr06155h | DOI Listing |
ChemSusChem
October 2024
Advanced Functional Nanomaterials group, Institute of Nano Science and Technology (INST), Knowledge City, Sector 81, SAS Nagar, Manauli PO, Mohali, 140306, Punjab, India.
Harnessing inexhaustible solar energy for CO valorization is a substantial step toward achieving a carbon-neutral energy cycle. However, CO conversion often exhibits slow kinetics, necessitating the utilization of sacrificial agents making the process economically unfeasible. In the ongoing quest for sustainable and economically feasible CO valorization, herein the photoreduction of CO to CO coupled with biomass-based alcohol oxidation to fine chemicals is reported via BiWO/g-CN (BWO/g-CN) 2D-2D nanosheet based S-scheme heterojunction.
View Article and Find Full Text PDFNat Commun
July 2024
Department of Chemistry, Sungkyunkwan University, 2066 Seobu-Ro, Suwon, 16419, Republic of Korea.
Currently, conventional dimethoxymethane synthesis methods are environmentally unfriendly. Here, we report a photo-redox catalysis system to generate dimethoxymethane using a silver and tungsten co-modified blue titanium dioxide catalyst (Ag.W-BTO) by coupling CO reduction and CHOH oxidation under mild conditions.
View Article and Find Full Text PDFChem Soc Rev
May 2024
Van 't Hoff Institute for Molecular Sciences, University of Amsterdam, PO box 94157, 1090 GD Amsterdam, The Netherlands.
Advances in the field of frustrated Lewis pair (FLP) chemistry have led to the discovery of radical pairs, obtained by a single-electron transfer (SET) from the Lewis base to the Lewis acid. Radical pairs are intriguing for their potential to enable cooperative activation of challenging substrates (, CH, N) in a homolytic fashion, as well as the exploration of novel radical reactions. In this review, we will cover the two known mechanisms of SET in FLPs-thermal and photoinduced-along with methods (, CV, DFT, UV-vis) to predict the mechanism and to characterise the involved electron donors and acceptors.
View Article and Find Full Text PDFInorg Chem
April 2024
Department of Inorganic and Physical Chemistry, Indian Institute of Science, Sir C.V. Raman Avenue, Bangalore 560012, India.
Boron-dipyrromethene (BODIPY) dyes are promising photosensitizers for cellular imaging and photodynamic therapy (PDT) owing to their excellent photophysical properties and the synthetically tunable core. Metalation provides a convenient way to overcome the drawbacks arising from their low aqueous solubility. New photo-/redox-responsive Co(III) prodrug chaperones are developed as anticancer PDT agents for efficient cellular delivery of red-light-active BODIPY dyes.
View Article and Find Full Text PDFInt J Mol Sci
March 2024
State Key Laboratory of Pulp and Paper Engineering, South China University of Technology, Guangzhou 510640, China.
Photoinduced metal-free ATRP has been successfully applied to fabricate thermo-responsive cellulose graft copolymer (PNIPAM--Cell) using 2-bromoisobuturyl bromide-modified cellulose as the macroinitiator. The polymerization of N-isopropylacrylamide (NIPAM) from cellulose was efficiently activated and deactivated with UV irradiation in the presence of an organic-based photo-redox catalyst. Both FTIR and C NMR analysis confirmed the structural similarity between the obtained PNIPAM--Cell and that synthesized via traditional ATRP methods.
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