The rapid reactions between Criegee intermediates and hydrogen halides play important roles in atmospheric chemistry, particularly in the polluted urban atmosphere. Employing a step-scan Fourier transform spectrometer, we recorded infrared absorption spectra of transient species and end products of the reaction CHCHOO + HCl in a flowing mixture of CHCHI/HCl/O/N irradiated at 308 nm. Bands at 1453.6, 1383.7, 1357.9, 1323.8, 1271.8, 1146.2, 1098.2, 1017.5, 931.5, and 847.0 cm were observed and assigned to the -conformer of chloroethyl hydroperoxide (-CEHP or CHCHClOOH). In addition, absorption bands of HO and acetyl chloride [CHC(O)Cl, at 1819.1 cm] were observed; some of them were produced from the secondary reactions of CHCHClO + O → CHC(O)Cl + HO and OH + HCl → HO + Cl, according to temporal profiles of HO and CHC(O)Cl. These secondary reactions are conceivable because the nascent formation of CHCHClO + OH via decomposition of internally excited CEHP was predicted by theory, and both HCl and O are major species in the system. The nascent formation of CHCHClO + OH appears to be more important than that of CHC(O)Cl + HO, consistent with theoretical predictions. By adding methanol to deplete some -CHCHOO, we observed only -CEHP with a reduced proportion; this observation indicates that the conversion from -CEHP, expected to be produced from -CHCHOO + HCl, to -CEHP is facile. We also estimated the overall rate coefficient of the reaction -/-CHCHOO + HCl to be = (2.7 ± 1.0) × 10 cm molecule s at ∼70 Torr and 298 K; this rate coefficient is about six times the only literature value = (4.77 ± 0.95) × 10 cm molecule s reported for -CHCHOO + HCl by Liu et al., indicating that -CHCHOO reacts with HCl much more rapidly than -CHCHOO.
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http://dx.doi.org/10.1021/acs.jpca.3c03527 | DOI Listing |
Langmuir
March 2025
School of Material Science and Engineering, University of Jinan, Jinan, 250022, PR China.
The construction of heterostructures promotes extending the light adsorption range of graphitic carbon nitride (g-CN) materials, improving the photogenerated charge carrier separation/transfer efficiency for attaining much enhanced performances. Because defective tungsten oxide (WO) materials possess rich composition/morphology and an extended light response in the near-infrared region, WO is a quite popular nanocomponent for modifying g-CN, forming heterostructures that can be used for various photocatalytic applications involving water splitting, CO reduction, NO removal, HO generation, and related chemical to fuel conversion reactions. In this review, important aspects of WO/g-CN heterostructure photocatalysts are reviewed to provide paradigms for composition adjustment, structural design, and photocatalytic applications of these materials.
View Article and Find Full Text PDFACS Appl Mater Interfaces
March 2025
Department of Chemistry, National Tsing Hua University, Hsinchu 300044, Taiwan.
To further demonstrate semiconductor facet effect to photocatalytic organic transformations and address a lack of using simple polyhedral semiconductor particles for disulfide bond formation, CuO cubes, octahedra, and rhombic dodecahedra were used to photocatalyze aerobic oxidation of 4-methylbenzenethiol. After reaction condition optimization, CuO crystals and ,,','-tetramethylethylenediamine (TMEDA) were added to 4-methylbenzenethiol in ethanol for thiol oxidation to 1,2-di--tolyldisulfane under 390 nm light-emitting diode (LED) lamp irradiation for just 5 min. Rhombic dodecahedra gave the highest product yield, followed by octahedra, cubes, and commercial CuO powder.
View Article and Find Full Text PDFSmall
March 2025
College of Materials Science and Engineering, Fuzhou University, Fuzhou, 350108, China.
The sluggish reaction kinetics and formidable shuttle effect of soluble lithium polysulfides (LiPSs) are thorny problems for the future industrialization of lithium-sulfur (Li-S) batteries. Therefore, exploring efficient electrocatalysts to capture LiPSs and accelerate their conversion is highly desirable yet tremendously challenging. Herein, a high-efficiency Bi/BiO/VMoN@rGO electrocatalyst with multifunctional active sites and multilevel heterointerfaces is elaborately designed for Li-S batteries.
View Article and Find Full Text PDFOrg Biomol Chem
March 2025
Univ Rouen Normandie, INSA Rouen Normandie, Univ Caen Normandie, ENSICAEN, CNRS, Institut CARMeN UMR 6064, F-76000 Rouen, France.
A visible-light-mediated chlorotrifluoromethylation catalyzed by a copper-based photo-redox catalyst of internal alkenes is reported. The reaction proceeds with complete regioselectivity under mild reaction conditions using commercially available FCSOCl as both the trifluoromethyl and chlorine source, leading to the synthesis of added-value chemicals with atom-economy. A vast array of internal alkenes were functionalized in decent to good yields, highlighting a great tolerance to various functional groups.
View Article and Find Full Text PDFAdv Mater
March 2025
Key Laboratory of Advanced Ceramics and Machining Technology of Ministry of Education, School of Materials Science and Engineering, Tianjin University, Tianjin, 300072, P. R. China.
Electrosynthesis of hydrogen peroxide (HO) via two-electron oxygen reduction reaction (2e ORR) is a promising alternative to the anthraquinone oxidation process. To improve the overall energy efficiency and economic viability of this catalytic process, one pathway is to develop advanced catalysts to decrease the overpotential at the cathode, and the other is to couple 2e ORR with certain anodic reactions to decrease the full cell voltage while producing valuable chemicals on both electrodes. The catalytic performance of a 2e ORR catalyst depends not only on the material itself but also on the environmental factors.
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