Catalysis for Green Chemistry
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 econom...
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| Формат: | Online |
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| Язык: | английский |
| Опубликовано: |
MDPI - Multidisciplinary Digital Publishing Institute
2024
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| Предметы: | |
| Online-ссылка: | ONIX_20240514_9783725809509_525 |
| Метки: |
Нет меток, Требуется 1-ая метка записи!
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| _version_ | 1869528507061633024 |
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| collection | Directory of Open Access Books |
| description | 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 | Online |
| id | doab-20.500.12854ir-137910 |
| institution | Directory of Open Access Books |
| language | eng |
| publishDate | 2024 |
| publishDateRange | 2024 |
| publishDateSort | 2024 |
| publisher | MDPI - Multidisciplinary Digital Publishing Institute |
| publisherStr | MDPI - Multidisciplinary Digital Publishing Institute |
| record_format | ojs |
| spelling | doab-20.500.12854ir-1379102024-05-14T14:55:27Z Catalysis for Green Chemistry Liu, Lu 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 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 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 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 thema EDItEUR::P Mathematics and Science::PN Chemistry::PNK Inorganic chemistry 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. 2024-05-14T14:55:21Z 2024-05-14T14:55:21Z 2024 book ONIX_20240514_9783725809509_525 9783725809509 9783725809493 https://directory.doabooks.org/handle/20.500.12854/137910 eng application/octet-stream Attribution-NonCommercial-NoDerivatives 4.0 International https://mdpi.com/books/pdfview/book/9174 https://mdpi.com/books/pdfview/book/9174 MDPI - Multidisciplinary Digital Publishing Institute 10.3390/books978-3-7258-0949-3 10.3390/books978-3-7258-0949-3 46cabcaa-dd94-4bfe-87b4-55023c1b36d0 9783725809509 9783725809493 252 open access |
| spellingShingle | 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 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 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 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 thema EDItEUR::P Mathematics and Science::PN Chemistry::PNK Inorganic chemistry Catalysis for Green Chemistry |
| title | Catalysis for Green Chemistry |
| title_full | Catalysis for Green Chemistry |
| title_fullStr | Catalysis for Green Chemistry |
| title_full_unstemmed | Catalysis for Green Chemistry |
| title_short | Catalysis for Green Chemistry |
| title_sort | catalysis for green chemistry |
| topic | 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 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 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 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 thema EDItEUR::P Mathematics and Science::PN Chemistry::PNK Inorganic chemistry |
| topic_facet | 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 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 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 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 thema EDItEUR::P Mathematics and Science::PN Chemistry::PNK Inorganic chemistry |
| url | ONIX_20240514_9783725809509_525 |