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It is shown here that carbamazepine (CBZ) would undergo direct photolysis and reaction with (•)OH as the main phototransformation pathways in surface waters. Environmental lifetimes are expected to vary from a few weeks to several months, and predictions are in good agreement with available field data. Acridine (I) and 10,11-dihydro-10,11-trans-dihydroxy-CBZ (V) are the main quantified phototransformation intermediates upon direct photolysis and (•)OH reaction, respectively. The photochemical yield of mutagenic I from CBZ is in the 3-3.5% range, and it is similar for both direct photolysis and (•)OH reaction: it would undergo limited variation with environmental conditions. In contrast, the yield of V would vary in the 4-8.5% range depending on the conditions, because V is formed from CBZ by (•)OH (9.0% yield) more effectively than upon direct photolysis (1.4% yield). Other important photointermediates, mostly formed from CBZ upon (•)OH reaction, are an aromatic-ring-dihydroxylated CBZ (VI) and N,N-bis(2-carboxyphenyl)urea (VII). Compounds VI and VII are formed by photochemistry and are not reported as human metabolites; thus, they could be used as tracers of CBZ phototransformation in surface waters. Interestingly, VI has recently been detected in river water.
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http://dx.doi.org/10.1021/es3015887 | DOI Listing |
Acc Chem Res
September 2025
Department of Chemistry, FRQNT Centre for Green Chemistry and Catalysis, McGill University, 801 Sherbrooke Street W, Montréal, Québec H3A 0B8, Canada.
ConspectusMolecular photochemistry, by harnessing the excited states of organic molecules, provides a platform fundamentally distinct from thermochemistry for generating reactive open-shell or spin-active species under mild conditions. Among its diverse applications, the resurgence of the Minisci-type reaction, a transformation historically reliant on thermally initiated radical conditions, has been fueled by modern photochemical strategies with improved efficiency and selectivity. Consequently, the photochemical Minisci-type reaction ranks among the most enabling methods for C()-H functionalizations of heteroarenes, which are of particular significance in medicinal chemistry for the rapid diversification of bioactive scaffolds.
View Article and Find Full Text PDFJ Hazard Mater
August 2025
State Key Laboratory of Water Pollution Control and Green Resource Recycling, School of the Environment, Nanjing University, Nanjing, China; Institute for the Environment and Health, Nanjing University Suzhou Campus, Suzhou, China. Electronic address:
The in-situ utilization of dissolved organic matter (DOM) for photosensitized activation of chemical oxidants towards micropollutant abatement presents a promising strategy aligned with the UN's Sustainable Development Goals. This study investigates the degradation of micropollutants via DOM-mediated photosensitized activation of peracetic acid (PAA) under solar irradiation and elucidates the underlying mechanisms. In wastewater effluent containing 5 mg/L DOM and 83 μM PAA, sunlight exposure facilitated DOM-mediated PAA activation, increasing the concentration of oxidative reactive species (ORS) by 50 % compared to DOM-free conditions.
View Article and Find Full Text PDFPhys Chem Chem Phys
August 2025
Max-Planck-Institute for Chemistry, Division of Atmospheric Chemistry, 55128 Mainz, Germany.
Trifluoroacetaldehyde (CFCHO) is formed in the atmosphere by the oxidation of a number of fluorinated, organic compounds of anthropogenic origin. The reaction of CFCHO with the OH radical is a potential source of atmospheric trifluoroacetic acid (TFA) which is a highly persistent, water-soluble compound that may accumulate in aquatic ecosystems and for which uncertainty about its sources, fate, and potential ecological impact persists. In light of growing concerns about the impact of TFA, we present the first study of the temperature dependence of the rate coefficient for the title reaction over the atmospherically relevant temperature range of 204 K to 361 K.
View Article and Find Full Text PDFJ Am Chem Soc
August 2025
Department of Chemistry and Biochemistry, University of California Los Angeles, Los Angeles, California 90095, United States.
Ni-catalyzed cross-coupling is a powerful strategy to forge C(sp)-C(sp) bonds. Typically, to do so requires overcoming a challenging C-C bond-forming reductive elimination, often enabled by the intermediacy of highly oxidized Ni species or outer-sphere processes. While direct C(sp)-C(sp) reductive elimination from the Ni base oxidation state is normally thermally inaccessible, light-activation provides an avenue to affect such transformations.
View Article and Find Full Text PDFEnviron Sci Process Impacts
August 2025
College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing 210095, China.
Ambroxol (AMB), a widely used expectorant drug, has been ubiquitously detected in aquatic environments due to its limited metabolism in the human body. Herein, we systematically investigated the photodegradation of AMB in waters upon natural sunlight irradiation. AMB has a p value of 8.
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