Reprint

Catalysis for Green Chemistry

Edited by
April 2024
252 pages
  • ISBN978-3-7258-0950-9 (Hardback)
  • ISBN978-3-7258-0949-3 (PDF)

This book is a reprint of the Special Issue Catalysis for Green Chemistry that was published in

Chemistry & Materials Science
Medicine & Pharmacology
Summary

Synthetic chemistry has greatly enriched people’s lives and dramatically changed the world in a multitude of aspects due to its impressive capacity to construct diverse functional groups and structurally complex molecules. However, traditional synthetic reactions normally suffer from low atom economy, harsh conditions, as well as hazardous waste production. Recently, the general principles of green chemistry have required the design of environmentally benign organic reactions, which is of great importance for the sustainable development of our society. Therein, it is pivotal to achieve new catalytic strategies for organic synthesis guided by the connotations of green chemistry.

The goal of this Special Issue was to collect original research papers and review articles devoted to all aspects of homogeneous and heterogeneous catalysis for green chemistry, including metal catalysis, organocatalysis, photocatalysis, and biocatalysis. The submission of manuscripts describing green catalytic technologies such as flow chemistry, multiphase catalysis, green reagents and solvents, catalyst immobilization, and recycling was also encouraged.

Format
  • Hardback
License and Copyright
© 2024 by the authors; CC BY-NC-ND license
Keywords
ionic liquids; acidic ionic liquids; supported ionic liquid phase; heterogeneous catalysis; silica; immobilization; sodium arenesulfinates; homocoupling; symmetric; diaryl sulfides; diaryl disulfides; pyrazolo[3,4-b]pyridine; alkyne activation; regional selectivity; 6-endo-dig cyclization; titanium dioxide; dihydroxyacetone; CO2 and NH3 microcalorimetry; FTIR of pyridine adsorption; acidity; basicity; dispersed copper particles; glycerol; propylene glycol; hydrogenolysis; heterogeneous catalysis; aminocarbonylation; green solvents; amides; palladium; homogeneous catalysis; copper catalysis; ortho-C(sp2)-H bond functionalization; naphthols; diazo compounds; metal carbene; density functional theory (DFT) calculations; boron Lewis acid; α-aryl nitrile; cyanation; isonitrile; green chemistry; polymeric ionic liquids; confined polymerization; laccase; immobilization; 2,4-DCP; removal; cinnamaldehyde; cinnamyl alcohol; CoRe bimetallic catalyst; selective hydrogenation; formic acid; propylene; propane; oxygen carrier; chemical looping; oxidative dehydrogenation; chitosan/PVA-stabilized copper nanoparticles; copper catalysis; heterogeneous catalyst; aqueous phase; recycle and reuse; sustainable enzymatic strategy; direct amide synthesis; green solvent; CALB; carboxylic acid; amine; chemical recycling; depolymerization; catalysis; glycolysis; transesterification; hydrolysis; cyclic ethers; tetrahydrofuran; supported catalyst; lactones; aerobic oxidation; oxygen

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