We have developed the continuous-flow synthesis of thioureas in a multicomponent reaction starting from isocyanides, amidines, or amines and sulfur. The aqueous polysulfide solution enabled the application of sulfur under homogeneous and mild conditions. The crystallized products were isolated by simple filtration after the removal of the co-solvent, and the sulfur retained in the mother liquid. Presenting a wide range of thioureas synthesized by this procedure confirms the utility of the convenient continuous-flow application of sulfur.
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http://dx.doi.org/10.3390/molecules26020303 | DOI Listing |
J Environ Manage
December 2024
Department of Water and Wastewater Engineering, School of Urban Construction, Wuhan University of Science and Technology, Wuhan, 430065, China. Electronic address:
The microalgal-bacterial granular sludge (MBGS) process shows potential for carbon-neutral wastewater treatment, yet its application in wastewater treatment plants remains underexplored. This study attempted to use a continuous-flow raceway reactor to treat real municipal wastewater using the MBGS process. The results showed that the removal efficiencies of organics peaked on the fifth day, while declining trends were observed for nitrogen and phosphorus removal.
View Article and Find Full Text PDFJ Phys Chem C Nanomater Interfaces
December 2024
The Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, Georgia 30332, United States.
We report a scalable method based on continuous-flow reactors for conformally coating the surfaces of facet-controlled Pd nanocrystals with uniform, ultrathin shells made of Pt. The key to the success of such an approach is the identification of a proper polyol to generate the Pt atoms at a relatively slow rate to ensure adequate surface diffusion and thus the formation of uniform shells in a layer-by-layer fashion. We first demonstrate the concept using the production of Pd@Pt (n = 2-5) core-shell icosahedral nanocrystals and then have the strategy successfully extended to the syntheses of Pd@Pt cubic and octahedral nanocrystals.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Zhengzhou University, College of Chemistry, and Pingyuan Laboratory, CHINA.
Transition-metal-regulated radical cross coupling enables the selective bonding of two distinct transient radicals, whereas the catalytic method for sorting two almost identical transient radicals, especially similar benzyl radicals, is still rare. Herein, we show that leveraging dual photoredox/cobalt catalysis can selectively couple two similar benzyl radicals. Using easily accessible methylarenes and phenylacetates (benzyl N-hydroxyphthalimide (NHPI) esters) as benzyl radical sources, a range of unsymmetrical 1,2-diarylethane classes via the 1°-1°, 1°-2°, 1°-3°, 2°-2°, 2°-3° and 3°-3° couplings were obtained with broad functional group tolerance.
View Article and Find Full Text PDFAdv Sci (Weinh)
December 2024
Shanghai Frontiers Science Center of Drug Target Identification and Delivery, School of Pharmaceutical Sciences, Shanghai Jiao Tong University, Shanghai, 200240, China.
Given the widespread presence of fluoroalkyl functionalities in bioactive molecules, the development of fluoroalkylation reactions with bench-stable and easy-to-use fluoroalkylating reagents is highly desirable. In addition, realization of mono-, di-, tri-, or polyfluoroalkyation usually requires distinct types of fluoroalkylating reagents under different or even harsh reaction conditions, and a universal method to accomplish different hydrofluoroalkylation of alkenes is lacking. Herein, the use of quaternary fluoroalkyl alcohols is reported as the universal fluoroalkylating reagents to readily facilitate mono-, di-, tri-, or polyfluoroalkylation of a wide range of alkene substrates in high yields.
View Article and Find Full Text PDFChemistry
December 2024
Fraunhofer Institute for Microengineering and Microsystems: Fraunhofer-Institut fur Mikrotechnik und Mikrosysteme IMM, Division Chemistry, Sustainable Syntheses Group, Carl-Zeiss-Straße 18-20, 55129, Mainz, GERMANY.
The selective decarboxylative fluorination of 3-oxo-3-phenylpropionic acid is used as a benchmark reaction to optimize it under biocompatible conditions in batch and to transfer it to continuous flow mode. The reaction conditions are varied with respect to temperature, fluorinating reagents, inorganic base additives, and pH, as these parameters have been identified as having a significant impact on the process. The formation of the products and any by-products is analyzed using gas chromatography (GC) and 19F nuclear magnetic resonance spectroscopy (NMR).
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