About: Sulfone is a research topic. Over the lifetime, 6922 publications have been published within this topic receiving 88966 citations. The topic is also known as: sulfones.
TL;DR: In this article, the authors present a review of the production and distribution of Dimethyl Sulfide in Marine Environments and its role in the emissions of Sulfur Dioxide.
Abstract: Biogenic Sulfur Emissions: A Review U.S. National Biogenic Sulfur Emissions Inventory Variability in Biogenic Sulfur Emissions from Florida Wetlands Synthesis and Emission of Hydrogen Sulfide by Higher Plants Sulfur Emissions from Roots of the Rain Forest Tree Stryphnodendron excelsum: Ecosystem, Community, and Physiological Implications Origin of Hydrogen Sulfide in Freshwater Sediments Sulfur Cycling in an Experimentally Acidified Seepage Lake Reactivity of Sulfur Nucleophiles Toward Halogenated Organic Compounds in Natural Waters The Distribution of Dimethyl Sulfide in the Oceans: A Review Biogeochemical Cycling of Dimethyl Sulfide in Marine Environments Dimethyl Sulfide Production in Marine Phytoplankton Dimethyl Sulfide and (Dimethylsulfonio)propionate in European Coastal and Shelf Waters Microbial Metabolism of Dimethyl Sulfide Metabolism of Acrylate and 3-Mercaptopropionate: Decomposition Products of (Dimethylsulfonio)propionate in Anoxic Marine Sediments Mechanistic Studies of Organosulfur (Thiol) Formation in Coastal Marine Sediments Reduced Sulfur Compounds in the Marine Environment: Analysis by High-Performance Liquid Chromatography Enzymatic Steps and Dissimilatory Sulfur Metabolism by Whole Cells of Anoxyphotobacteria Thermodynamics and Kinetics of Hydrogen Sulfide in Natural Waters Hydrogen Sulfides in Oxic Seawater Dimethyl Sulfide and Hydrogen Sulfide in Marine Air Distribution of Biogenic Sulfur Compounds in the Remote Southern Hemisphere Sulfur Isotope Ratios: Tracers of Non-Sea Salt Sulfate in the Remote Atmosphere Two Automated Methods for Measuring Trace Levels of Sulfur Dioxide Using Translation Reactions Gas-Phase Atmospheric Oxidation of Biogenic Sulfur Compounds: A Review OH-Initiated Oxidation of Biogenic Sulfur Compounds: Kinetics and Mechanisms Under Atmospheric Conditions Mechanism of Atmospheric Oxidation of Sulfur Dioxide by Hydroxyl Radicals Mechanisms for the Reaction of CH[3S with NO[2 The Impact of Halogen Oxides on Dimethyl Sulfide Oxidation in the Marine Atmosphere Fourier Transform IR Studies of the Reactions of Dimethyl Sulfoxide with OH, NO[3, and Cl Radicals North Sea Dimethyl Sulfide Emissions as a Source of Background Sulfate over Scandinavia: A Model The Uptake of Gases by Liquid Droplets: Sulfur Dioxide Rate of Reaction of Methanesulfonic Acid, Dimethyl Sulfoxide, and Dimethyl Sulfone with Hydroxyl Radical in Aqueous Solution Oxidation of Biogenic Sulfur Compounds in Aqueous Media: Kinetics and Environmental Implications
TL;DR: A selective catalytic meta sulfonation of 2-phenylpyridines was found to occur in the presence of (arene)ruthenium(II) complexes upon reaction with sulfonyl chlorides, offering access to atypical regioselectivity for reactions involving chelation-assisted cyclometalation.
Abstract: A selective catalytic meta sulfonation of 2-phenylpyridines was found to occur in the presence of (arene)ruthenium(II) complexes upon reaction with sulfonyl chlorides. The 2-pyridyl group facilitates the formation of a stable Ru–Caryl σ bond that induces a strong para-directing effect. Electrophilic aromatic substitution proceeds with the sulfonyl chloride to furnish a sulfone at the position meta to the chelating group. This new catalytic process offers access to atypical regioselectivity for reactions involving chelation-assisted cyclometalation.
TL;DR: Aromatic and aliphatic sulfides are oxidized to sulfoxides or sulfones in high yield with 30% hydrogen peroxide under organic solvent-and halogen-free conditions as discussed by the authors.
TL;DR: The most active dibenzo[b,d]thiophene sulfone co‐polymer has a UV photocatalytic activity that rivals TiO2, but is much more active under visible light.
Abstract: Linear poly(p-phenylene)s are modestly active UV photocatalysts for hydrogen production in the presence of a sacrificial electron donor. Introduction of planarized fluorene, carbazole, dibenzo[b,d]thiophene or dibenzo[b,d]thiophene sulfone units greatly enhances the H2 evolution rate. The most active dibenzo[b,d]thiophene sulfone co-polymer has a UV photocatalytic activity that rivals TiO2, but is much more active under visible light. The dibenzo[b,d]thiophene sulfone co-polymer has an apparent quantum yield of 2.3 % at 420 nm, as compared to 0.1 % for platinized commercial pristine carbon nitride.
TL;DR: In this article, the hydrophilic modification of poly(ether sulfone) UF membrane was performed by self-assembly of the hydroxyl group of TiO 2 nanoparticle surface and the sulfone group and ether bond in poly(et.al) structure through coordination and hydrogen bond interaction.