Highly vibrationally excited disulfur S in the XΣ and aΔ states has been detected in the gaseous mixture of O and OCS irradiated with light at 266 nm. Generation of CO in the reaction system has been reported; however, no direct detection of sulfur atoms (S(P) and S(D)) has been made. In the present study, we have employed the two-photon laser-induced fluorescence (2P-LIF) technique to detect S(P) and S(D) directly and recorded the time profiles of the atoms at varying pressures of OCS. Kinetic analyses of the profiles show that (i) S(D) is generated in the O(D) + OCS reaction and consumed by the S(D) + OCS reaction, and (ii) S(P) is mainly generated in the O(D) + OCS reaction instead of quenching of S(D) by collisions with OCS and ambient gases. The vibrational levels v = 19 and 10 of the respective electronic states XΣ and aΔ of S were detected in the O/OCS/266 nm system. The two vibrational levels cannot be generated by the available energy of the S(P) + OCS reaction, giving evidence that S in the XΣ and aΔ states are generated by the S(D) + OCS reaction.
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http://dx.doi.org/10.1021/acs.jpca.7b11375 | DOI Listing |
ACS Omega
December 2024
New Drug Development Center (NDDC), Daegu-Gyeongbuk Medical Innovation Foundation (DGMIF), 80 Cheombok-ro, Dong-gu, Daegu 41061, Republic of Korea.
A mild and general method for photoredox-catalyzed trifluoromethylative and pentafluoroethylative heterofunctionalization of alkenes is proposed. In this reaction, the Togni reagent serves as a CF- or CFCF-radical source for the regioselective formation of the C-CF and C-CFCF bonds from alkenes, and additional nucleophiles (O, S, N) provide C-O, C-S, and C-N bonds, respectively. These reactions provide a common gateway to access the fluoroalkylative heterofunctionalization of alkenes.
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November 2024
College of Chemistry and Chemical Engineering, Qingdao University Qingdao 266071 China
The naturally sluggish redox kinetics and limited utilization associated with the sulfur conversion in Zn/S electrochemistry hinder its real application. Herein, we report an phase reconstruction strategy that activates the catalytic activity of vanadium oxides for invoking redox-catalysis to manipulate reversible sulfur conversion. It was identified that the VO@C/S precursor derived from metal organic frameworks could be transformed into VO ·HO@C/S by a facile electrochemical induction process.
View Article and Find Full Text PDFAntibiotics (Basel)
October 2024
Department of Clinical Medicine and Surgery, Section of Infectious Diseases, University of Naples Federico II, 80131 Naples, Italy.
Carbapenem-resistant (CRAB) poses significant challenges in healthcare due to its multidrug resistance and high mortality rates among critically ill patients. We enrolled 45 patients. Cefiderocol was administered to 40% of patients, often (38.
View Article and Find Full Text PDFFood Chem
February 2025
Institute of Biomass and Function Materials & National Demonstration Centre for Experimental Light Chemistry Engineering Education, College of Bioresources Chemistry and Materials Engineering, Shaanxi University of Science and Technology, Xi'an 710021, PR China.
This study was conducted primarily to develop an environment-friendly food packaging boasting several advantages, including good water vapor barrier, UV resistance, antimicrobial activity, non-leachability, and polymer miscibility. Initially, the starch-based antimicrobial agent (OCSI) was synthesized through a simple esterification reaction between oxidized corn starch (OCS) and indoleacetic acid (IAA). Subsequently, OCSI was further blended separately with environmentally-friendly materials (PVA, PBAT, PCL), and a series of environment-friendly packaging films were successfully prepared.
View Article and Find Full Text PDFMolecules
October 2024
IMT Nord Europe, Institut Mines-Télécom, Centre for Energy and Environment, University Lille, 59000 Lille, France.
The gas phase reaction of fluorine atoms with carbonyl sulfide, F + OCS → SF + CO (1), has been investigated over a wide temperature range, T = 220-960 K, in a discharge-flow system combined with mass spectrometry for the analysis of the reactive mixture. The reaction rate coefficient was determined as a function of temperature using both absolute (under pseudo-first-order conditions using an excess of F atoms) and relative rate methods: = (8.95 ± 0.
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