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Asymmetric oxidation reactions : a practical approach in chemistry / edited by Tsutomu Katsuki
| Asymmetric oxidation reactions : a practical approach in chemistry / edited by Tsutomu Katsuki |
| Pubbl/distr/stampa | New York : Oxford University Press, c2001 |
| Descrizione fisica | XVIII, 244 p. ; 24 cm. |
| Disciplina | 660.28443 |
| Collana | The practical approach in chemistry series |
| Soggetto topico | Ossidazione |
| ISBN | 0-19-850201-X |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNIBAS-000011948 |
| New York : Oxford University Press, c2001 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. della Basilicata | ||
| ||
Iridium-catalyzed asymmetric hydrogenation of furan derivatives and thiophene 1,1-dioxides / / von Larissa Pauli
| Iridium-catalyzed asymmetric hydrogenation of furan derivatives and thiophene 1,1-dioxides / / von Larissa Pauli |
| Autore | Pauli Larissa |
| Pubbl/distr/stampa | Gottingen, [Germany] : , : Cuvillier Verlag, , 2014 |
| Descrizione fisica | 1 online resource (179 pages) |
| Disciplina | 660.28443 |
| Soggetto topico |
Hydrogenation
Thiophenes |
| Soggetto genere / forma | Electronic books. |
| ISBN | 3-7369-4851-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910511894503321 |
Pauli Larissa
|
||
| Gottingen, [Germany] : , : Cuvillier Verlag, , 2014 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Iridium-catalyzed asymmetric hydrogenation of furan derivatives and thiophene 1,1-dioxides / / von Larissa Pauli
| Iridium-catalyzed asymmetric hydrogenation of furan derivatives and thiophene 1,1-dioxides / / von Larissa Pauli |
| Autore | Pauli Larissa |
| Pubbl/distr/stampa | Gottingen, [Germany] : , : Cuvillier Verlag, , 2014 |
| Descrizione fisica | 1 online resource (179 pages) |
| Disciplina | 660.28443 |
| Soggetto topico |
Hydrogenation
Thiophenes |
| ISBN | 3-7369-4851-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910794956603321 |
|
Pauli Larissa
|
||
| Gottingen, [Germany] : , : Cuvillier Verlag, , 2014 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Iridium-catalyzed asymmetric hydrogenation of furan derivatives and thiophene 1,1-dioxides / / von Larissa Pauli
| Iridium-catalyzed asymmetric hydrogenation of furan derivatives and thiophene 1,1-dioxides / / von Larissa Pauli |
| Autore | Pauli Larissa |
| Pubbl/distr/stampa | Gottingen, [Germany] : , : Cuvillier Verlag, , 2014 |
| Descrizione fisica | 1 online resource (179 pages) |
| Disciplina | 660.28443 |
| Soggetto topico |
Hydrogenation
Thiophenes |
| ISBN | 3-7369-4851-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910808166703321 |
|
Pauli Larissa
|
||
| Gottingen, [Germany] : , : Cuvillier Verlag, , 2014 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Metal catalysed carbon-carbon bond-forming reactions [[electronic resource] /] / edited by Stanley M. Roberts ... [et al.]
| Metal catalysed carbon-carbon bond-forming reactions [[electronic resource] /] / edited by Stanley M. Roberts ... [et al.] |
| Pubbl/distr/stampa | Chichester, West Sussex, England ; ; Hoboken, N.J., : John Wiley, c2004 |
| Descrizione fisica | 1 online resource (282 p.) |
| Disciplina |
660
660.28443 660.2995 |
| Altri autori (Persone) | RobertsStanley M |
| Collana | Catalysts for fine chemical synthesis |
| Soggetto topico |
Organic compounds - Synthesis
Metal catalysts Chemical bonds |
| ISBN |
1-280-27141-8
9786610271412 0-470-34184-X 0-470-86201-7 0-470-86200-9 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Catalysts for Fine Chemical Synthesis Volume 3; Contents; Series Preface; Preface to Volume 3; Abbreviations; List of Chemical Names Used; 1 Considerations of Industrial Fine Chemical Synthesis; 1.1 Introduction; 1.2 Types of processes - flow charts; 1.2.1 Classical process; 1.2.2 General catalytic process; 1.3 Costs associated with use of catalysts; 1.3.1 Catalyst fabrication costs; 1.3.2 Intellectual property right (IPR) issues; 1.3.3 Separation costs; 1.3.4 Pre-reaction/immobilisation; 1.3.5 Post reaction - separation; 1.3.6 Industrial examples; References
2 Alkylation and Allylation Adjacent to a Carbonyl Group2.1 The RuH(2)(CO)(PPh(3))(3)-catalysed alkylation, alkenylation and arylation of aromatic ketones via carbon-hydrogen bond cleavage; 2.1.1 Preparation of carbonyldihydrotris(triphenylphosphine) ruthenium; 2.1.2 Synthesis of 8-(2-triethoxysilanylethyl)-3,4-dihydro-2H-naphthalen-1-one; 2.1.3 Synthesis of 8-(1-methyl-2-trimethylsilanylvinyl)-3,4-dihydro-2H-naphthalen-1-one; 2.1.4 Synthesis of 1-biphenyl-2-yl-2,2-dimethylpropan-1-one; 2.1.5 Conclusion; References 2.2 Catalytic, asymmetric synthesis of a,a-disubstituted amino acids using a chiral copper-salen complex as a phase transfer catalyst2.2.1 Synthesis of (chsalen); 2.2.2 Synthesis of copper(II) (chsalen); 2.2.3 Alkylation of alanine methyl ester Schiff base by chiral salen-metal catalysts, a-benzyl-alanine methyl ester; 2.2.4 Conclusion; References; 2.3 Asymmetric phase-transfer catalysed alkylation of glycine imines using cinchona alkaloid derived quaternary ammonium salts 2.3.1 Synthesis of (1S,2S,4S,5R,1 ́R)-1-(anthracen-9-ylmethyl)-5-ethyl-2-[hydroxy(quinolin-4-yl)methyl]-1-azoniabicyclo[2.2.2]octane bromide2.3.2 Synthesis of (1S,2S,4S,5R,1 ́R)-1-(anthracen-9-ylmethyl)-5-ethyl-2-[benzyloxy(quinolin-4-yl)methyl]-1-azoniabicyclo[2.2.2]octane bromide; 2.3.3 Synthesis of (2S)-tert-butyl 2-amino-4-bromopent-4-enoate; 2.3.4 Conclusion; References; 3 Asymmetric Alkylation or Amination of Allylic Esters; 3.1 Synthesis and application in palladium-catalysed asymmetric allylic substitution of enantiopure cyclic b-iminophosphine ligands 3.1.1 Synthesis of (2,6-dimethyl-phenyl)-(1-phenyl-2,3,3a,8a-tetrahydro-1H-1-phospha-cyclopenta[a]inden-8-ylidene)-amines 1R(p)3.1.2 Synthesis of (E)-Methyl 2-carbomethoxy-3,5-diphenylpent-4-enoate; 3.1.3 Synthesis of benzyl(1,3-diphenylprop-2-enyl)amine; 3.1.4 Conclusion; References; 3.2 (9H,9 ́H,10H,10 ́H,11H,11H ́,13H,13 ́H,14H,14 ́H,15H,15 ́H-perfluorotricosane-12,12 ́-diyl)bis[(4S)-4-phenyl-2-oxazoline as a ligand for asymmetric palladium-catalysed alkylation of allylic acetates in fluorous media; 3.2.1 Synthesis of 2-iodo-1-(1H,1 ́H,2H,2 ́H,3H,3 ́H-perfluorooctyl)-3-propanol 3.2.2 Synthesis of 3-(1H,1 ́H,2H,2 ́H,3H,3 ́H-perfluorooctyl)-1-propanol |
| Record Nr. | UNINA-9910144299903321 |
| Chichester, West Sussex, England ; ; Hoboken, N.J., : John Wiley, c2004 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Metal catalysed carbon-carbon bond-forming reactions [[electronic resource] /] / edited by Stanley M. Roberts ... [et al.]
| Metal catalysed carbon-carbon bond-forming reactions [[electronic resource] /] / edited by Stanley M. Roberts ... [et al.] |
| Pubbl/distr/stampa | Chichester, West Sussex, England ; ; Hoboken, N.J., : John Wiley, c2004 |
| Descrizione fisica | 1 online resource (282 p.) |
| Disciplina |
660
660.28443 660.2995 |
| Altri autori (Persone) | RobertsStanley M |
| Collana | Catalysts for fine chemical synthesis |
| Soggetto topico |
Organic compounds - Synthesis
Metal catalysts Chemical bonds |
| ISBN |
1-280-27141-8
9786610271412 0-470-34184-X 0-470-86201-7 0-470-86200-9 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Catalysts for Fine Chemical Synthesis Volume 3; Contents; Series Preface; Preface to Volume 3; Abbreviations; List of Chemical Names Used; 1 Considerations of Industrial Fine Chemical Synthesis; 1.1 Introduction; 1.2 Types of processes - flow charts; 1.2.1 Classical process; 1.2.2 General catalytic process; 1.3 Costs associated with use of catalysts; 1.3.1 Catalyst fabrication costs; 1.3.2 Intellectual property right (IPR) issues; 1.3.3 Separation costs; 1.3.4 Pre-reaction/immobilisation; 1.3.5 Post reaction - separation; 1.3.6 Industrial examples; References
2 Alkylation and Allylation Adjacent to a Carbonyl Group2.1 The RuH(2)(CO)(PPh(3))(3)-catalysed alkylation, alkenylation and arylation of aromatic ketones via carbon-hydrogen bond cleavage; 2.1.1 Preparation of carbonyldihydrotris(triphenylphosphine) ruthenium; 2.1.2 Synthesis of 8-(2-triethoxysilanylethyl)-3,4-dihydro-2H-naphthalen-1-one; 2.1.3 Synthesis of 8-(1-methyl-2-trimethylsilanylvinyl)-3,4-dihydro-2H-naphthalen-1-one; 2.1.4 Synthesis of 1-biphenyl-2-yl-2,2-dimethylpropan-1-one; 2.1.5 Conclusion; References 2.2 Catalytic, asymmetric synthesis of a,a-disubstituted amino acids using a chiral copper-salen complex as a phase transfer catalyst2.2.1 Synthesis of (chsalen); 2.2.2 Synthesis of copper(II) (chsalen); 2.2.3 Alkylation of alanine methyl ester Schiff base by chiral salen-metal catalysts, a-benzyl-alanine methyl ester; 2.2.4 Conclusion; References; 2.3 Asymmetric phase-transfer catalysed alkylation of glycine imines using cinchona alkaloid derived quaternary ammonium salts 2.3.1 Synthesis of (1S,2S,4S,5R,1 ́R)-1-(anthracen-9-ylmethyl)-5-ethyl-2-[hydroxy(quinolin-4-yl)methyl]-1-azoniabicyclo[2.2.2]octane bromide2.3.2 Synthesis of (1S,2S,4S,5R,1 ́R)-1-(anthracen-9-ylmethyl)-5-ethyl-2-[benzyloxy(quinolin-4-yl)methyl]-1-azoniabicyclo[2.2.2]octane bromide; 2.3.3 Synthesis of (2S)-tert-butyl 2-amino-4-bromopent-4-enoate; 2.3.4 Conclusion; References; 3 Asymmetric Alkylation or Amination of Allylic Esters; 3.1 Synthesis and application in palladium-catalysed asymmetric allylic substitution of enantiopure cyclic b-iminophosphine ligands 3.1.1 Synthesis of (2,6-dimethyl-phenyl)-(1-phenyl-2,3,3a,8a-tetrahydro-1H-1-phospha-cyclopenta[a]inden-8-ylidene)-amines 1R(p)3.1.2 Synthesis of (E)-Methyl 2-carbomethoxy-3,5-diphenylpent-4-enoate; 3.1.3 Synthesis of benzyl(1,3-diphenylprop-2-enyl)amine; 3.1.4 Conclusion; References; 3.2 (9H,9 ́H,10H,10 ́H,11H,11H ́,13H,13 ́H,14H,14 ́H,15H,15 ́H-perfluorotricosane-12,12 ́-diyl)bis[(4S)-4-phenyl-2-oxazoline as a ligand for asymmetric palladium-catalysed alkylation of allylic acetates in fluorous media; 3.2.1 Synthesis of 2-iodo-1-(1H,1 ́H,2H,2 ́H,3H,3 ́H-perfluorooctyl)-3-propanol 3.2.2 Synthesis of 3-(1H,1 ́H,2H,2 ́H,3H,3 ́H-perfluorooctyl)-1-propanol |
| Record Nr. | UNINA-9910831084803321 |
| Chichester, West Sussex, England ; ; Hoboken, N.J., : John Wiley, c2004 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Modern heterogeneous oxidation catalysis [[electronic resource] ] : design, reactions and characterization / / edited by Noritaka Mizuno
| Modern heterogeneous oxidation catalysis [[electronic resource] ] : design, reactions and characterization / / edited by Noritaka Mizuno |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH |
| Descrizione fisica | 1 online resource (359 p.) |
| Disciplina | 660.28443 |
| Altri autori (Persone) | MizunoNoritaka |
| Soggetto topico |
Heterogeneous catalysis
Oxidation |
| ISBN |
1-282-46095-1
9786612460951 3-527-62754-5 3-527-62755-3 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Modern Heterogeneous Oxidation Catalysis: Design, Reactions and Characterization; Contents; Preface; List of Contributors; 1 Concepts in Selective Oxidation of Small Alkane Molecules; 1.1 Introduction; 1.2 The Research Field; 1.3 Substrate Activation; 1.4 Active Oxygen Species; 1.5 Catalyst Material Science; 1.6 Conclusion; References; 2 Active Ensemble Structures for Selective Oxidation Catalyses at Surfaces; 2.1 Introduction; 2.2 Chiral Self-Dimerization of Vanadium Schiff-Base Complexes on SiO2 and Their Catalytic Performances for Asymmetric Oxidative Coupling of 2-Naphthol
2.2.1 Asymmetric Heterogeneous Catalysis Using Supported Metal Complexes2.2.2 Chiral V-Dimer Structure on a SiO2 Surface; 2.2.3 Asymmetric Catalysis for Oxidative Coupling of 2-Naphthol to BINOL; 2.3 Low-Temperature Preferential Oxidation of CO in Excess H2 on Cu-Clusters Dispersed on CeO2; 2.3.1 Preferential Oxidation (PROX) of CO in Excess H2 on Novel Metal Catalysts; 2.3.2 Characterization and Performance of a Novel Cu Cluster/CeO2 Catalyst; 2.4 Direct Phenol Synthesis from Benzene and Molecular Oxygen on a Novel N-Interstitial Re10-Cluster/HZSM-5 Catalyst 2.4.1 Phenol Production from Benzene with N2O, H2 + O2, and O22.4.1.1 Benzene to Phenol with N2O; 2.4.1.2 Benzene to Phenol with H2 + O2; 2.4.1.3 Benzene to Phenol with O2; 2.4.2 Novel Re/HZSM-5 Catalyst for Direct Benzene-to-Phenol Synthesis with O2; 2.4.3 Active Re Clusters Entrapped in ZSM-5 Pores; 2.4.4 Structural Dynamics of the Active Re10 Cluster; 2.5 Conclusion; References; 3 Unique Catalytic Performance of Supported Gold Nanoparticles in Oxidation; 3.1 Introduction; 3.2 Low-Temperature CO Oxidation; 3.2.1 Low-Temperature CO Oxidation in Air 3.2.1.1 Junction Perimeter Between Au Particles and the Support3.2.1.2 Selection of Suitable Supports; 3.2.1.3 Sensitivity to the Size of the Gold Particles; 3.2.2 Low-Temperature CO Oxidation in H2; 3.2.3 Mechanism for CO Oxidation Over Supported Gold Nanoparticles; 3.2.3.1 Mechanisms Involving Junction Perimeter Between Gold and the Metal-Oxide Supports; 3.2.3.2 Mechanisms Involving Specific Size or Thickness of Gold Clusters or Thin Layers; 3.2.3.3 Mechanisms Involving Cationic Gold; 3.3 Complete Oxidation of Volatile Organic Compounds 3.4 Gas-Phase Selective Oxidation of Organic Compounds3.4.1 Gas-Phase Selective Oxidation of Aliphatic Alkanes; 3.4.2 Gas-Phase Selective Oxidation of Alcohols; 3.4.3 Gas-Phase Propylene Epoxidation; 3.4.3.1 Introduction; 3.4.3.2 Gas-Phase Propylene Epoxidation with Hydrogen-Oxygen Mixtures on Au/TiO2; 3.4.3.3 Gas-Phase Propylene Epoxidation with Hydrogen-Oxygen Mixtures on Au/Ti-SiO2; 3.5 Liquid-Phase Selective Oxidation of Organic Compounds; 3.5.1 Oxidation of Mono-Alcohols; 3.5.2 Oxidation of Diols; 3.5.3 Oxidation of Glycerol; 3.5.4 Aerobic Oxidation of Glucose 3.5.5 Oxidation of Alkanes and Alkenes |
| Record Nr. | UNINA-9910139467703321 |
| Weinheim, : Wiley-VCH | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Modern heterogeneous oxidation catalysis [[electronic resource] ] : design, reactions and characterization / / edited by Noritaka Mizuno
| Modern heterogeneous oxidation catalysis [[electronic resource] ] : design, reactions and characterization / / edited by Noritaka Mizuno |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH |
| Descrizione fisica | 1 online resource (359 p.) |
| Disciplina | 660.28443 |
| Altri autori (Persone) | MizunoNoritaka |
| Soggetto topico |
Heterogeneous catalysis
Oxidation |
| ISBN |
1-282-46095-1
9786612460951 3-527-62754-5 3-527-62755-3 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Modern Heterogeneous Oxidation Catalysis: Design, Reactions and Characterization; Contents; Preface; List of Contributors; 1 Concepts in Selective Oxidation of Small Alkane Molecules; 1.1 Introduction; 1.2 The Research Field; 1.3 Substrate Activation; 1.4 Active Oxygen Species; 1.5 Catalyst Material Science; 1.6 Conclusion; References; 2 Active Ensemble Structures for Selective Oxidation Catalyses at Surfaces; 2.1 Introduction; 2.2 Chiral Self-Dimerization of Vanadium Schiff-Base Complexes on SiO2 and Their Catalytic Performances for Asymmetric Oxidative Coupling of 2-Naphthol
2.2.1 Asymmetric Heterogeneous Catalysis Using Supported Metal Complexes2.2.2 Chiral V-Dimer Structure on a SiO2 Surface; 2.2.3 Asymmetric Catalysis for Oxidative Coupling of 2-Naphthol to BINOL; 2.3 Low-Temperature Preferential Oxidation of CO in Excess H2 on Cu-Clusters Dispersed on CeO2; 2.3.1 Preferential Oxidation (PROX) of CO in Excess H2 on Novel Metal Catalysts; 2.3.2 Characterization and Performance of a Novel Cu Cluster/CeO2 Catalyst; 2.4 Direct Phenol Synthesis from Benzene and Molecular Oxygen on a Novel N-Interstitial Re10-Cluster/HZSM-5 Catalyst 2.4.1 Phenol Production from Benzene with N2O, H2 + O2, and O22.4.1.1 Benzene to Phenol with N2O; 2.4.1.2 Benzene to Phenol with H2 + O2; 2.4.1.3 Benzene to Phenol with O2; 2.4.2 Novel Re/HZSM-5 Catalyst for Direct Benzene-to-Phenol Synthesis with O2; 2.4.3 Active Re Clusters Entrapped in ZSM-5 Pores; 2.4.4 Structural Dynamics of the Active Re10 Cluster; 2.5 Conclusion; References; 3 Unique Catalytic Performance of Supported Gold Nanoparticles in Oxidation; 3.1 Introduction; 3.2 Low-Temperature CO Oxidation; 3.2.1 Low-Temperature CO Oxidation in Air 3.2.1.1 Junction Perimeter Between Au Particles and the Support3.2.1.2 Selection of Suitable Supports; 3.2.1.3 Sensitivity to the Size of the Gold Particles; 3.2.2 Low-Temperature CO Oxidation in H2; 3.2.3 Mechanism for CO Oxidation Over Supported Gold Nanoparticles; 3.2.3.1 Mechanisms Involving Junction Perimeter Between Gold and the Metal-Oxide Supports; 3.2.3.2 Mechanisms Involving Specific Size or Thickness of Gold Clusters or Thin Layers; 3.2.3.3 Mechanisms Involving Cationic Gold; 3.3 Complete Oxidation of Volatile Organic Compounds 3.4 Gas-Phase Selective Oxidation of Organic Compounds3.4.1 Gas-Phase Selective Oxidation of Aliphatic Alkanes; 3.4.2 Gas-Phase Selective Oxidation of Alcohols; 3.4.3 Gas-Phase Propylene Epoxidation; 3.4.3.1 Introduction; 3.4.3.2 Gas-Phase Propylene Epoxidation with Hydrogen-Oxygen Mixtures on Au/TiO2; 3.4.3.3 Gas-Phase Propylene Epoxidation with Hydrogen-Oxygen Mixtures on Au/Ti-SiO2; 3.5 Liquid-Phase Selective Oxidation of Organic Compounds; 3.5.1 Oxidation of Mono-Alcohols; 3.5.2 Oxidation of Diols; 3.5.3 Oxidation of Glycerol; 3.5.4 Aerobic Oxidation of Glucose 3.5.5 Oxidation of Alkanes and Alkenes |
| Record Nr. | UNINA-9910831081903321 |
| Weinheim, : Wiley-VCH | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Modern heterogeneous oxidation catalysis : design, reactions and characterization / / edited by Noritaka Mizuno
| Modern heterogeneous oxidation catalysis : design, reactions and characterization / / edited by Noritaka Mizuno |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH |
| Descrizione fisica | 1 online resource (359 p.) |
| Disciplina | 660.28443 |
| Altri autori (Persone) | MizunoNoritaka |
| Soggetto topico |
Heterogeneous catalysis
Oxidation |
| ISBN |
9786612460951
9781282460959 1282460951 9783527627547 3527627545 9783527627554 3527627553 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Modern Heterogeneous Oxidation Catalysis: Design, Reactions and Characterization; Contents; Preface; List of Contributors; 1 Concepts in Selective Oxidation of Small Alkane Molecules; 1.1 Introduction; 1.2 The Research Field; 1.3 Substrate Activation; 1.4 Active Oxygen Species; 1.5 Catalyst Material Science; 1.6 Conclusion; References; 2 Active Ensemble Structures for Selective Oxidation Catalyses at Surfaces; 2.1 Introduction; 2.2 Chiral Self-Dimerization of Vanadium Schiff-Base Complexes on SiO2 and Their Catalytic Performances for Asymmetric Oxidative Coupling of 2-Naphthol
2.2.1 Asymmetric Heterogeneous Catalysis Using Supported Metal Complexes2.2.2 Chiral V-Dimer Structure on a SiO2 Surface; 2.2.3 Asymmetric Catalysis for Oxidative Coupling of 2-Naphthol to BINOL; 2.3 Low-Temperature Preferential Oxidation of CO in Excess H2 on Cu-Clusters Dispersed on CeO2; 2.3.1 Preferential Oxidation (PROX) of CO in Excess H2 on Novel Metal Catalysts; 2.3.2 Characterization and Performance of a Novel Cu Cluster/CeO2 Catalyst; 2.4 Direct Phenol Synthesis from Benzene and Molecular Oxygen on a Novel N-Interstitial Re10-Cluster/HZSM-5 Catalyst 2.4.1 Phenol Production from Benzene with N2O, H2 + O2, and O22.4.1.1 Benzene to Phenol with N2O; 2.4.1.2 Benzene to Phenol with H2 + O2; 2.4.1.3 Benzene to Phenol with O2; 2.4.2 Novel Re/HZSM-5 Catalyst for Direct Benzene-to-Phenol Synthesis with O2; 2.4.3 Active Re Clusters Entrapped in ZSM-5 Pores; 2.4.4 Structural Dynamics of the Active Re10 Cluster; 2.5 Conclusion; References; 3 Unique Catalytic Performance of Supported Gold Nanoparticles in Oxidation; 3.1 Introduction; 3.2 Low-Temperature CO Oxidation; 3.2.1 Low-Temperature CO Oxidation in Air 3.2.1.1 Junction Perimeter Between Au Particles and the Support3.2.1.2 Selection of Suitable Supports; 3.2.1.3 Sensitivity to the Size of the Gold Particles; 3.2.2 Low-Temperature CO Oxidation in H2; 3.2.3 Mechanism for CO Oxidation Over Supported Gold Nanoparticles; 3.2.3.1 Mechanisms Involving Junction Perimeter Between Gold and the Metal-Oxide Supports; 3.2.3.2 Mechanisms Involving Specific Size or Thickness of Gold Clusters or Thin Layers; 3.2.3.3 Mechanisms Involving Cationic Gold; 3.3 Complete Oxidation of Volatile Organic Compounds 3.4 Gas-Phase Selective Oxidation of Organic Compounds3.4.1 Gas-Phase Selective Oxidation of Aliphatic Alkanes; 3.4.2 Gas-Phase Selective Oxidation of Alcohols; 3.4.3 Gas-Phase Propylene Epoxidation; 3.4.3.1 Introduction; 3.4.3.2 Gas-Phase Propylene Epoxidation with Hydrogen-Oxygen Mixtures on Au/TiO2; 3.4.3.3 Gas-Phase Propylene Epoxidation with Hydrogen-Oxygen Mixtures on Au/Ti-SiO2; 3.5 Liquid-Phase Selective Oxidation of Organic Compounds; 3.5.1 Oxidation of Mono-Alcohols; 3.5.2 Oxidation of Diols; 3.5.3 Oxidation of Glycerol; 3.5.4 Aerobic Oxidation of Glucose 3.5.5 Oxidation of Alkanes and Alkenes |
| Record Nr. | UNINA-9911020085803321 |
| Weinheim, : Wiley-VCH | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Selective oxidation by heterogeneous catalysis / Gabriele Centi, Fabrizio Cavani, Ferruccio Trifirò
| Selective oxidation by heterogeneous catalysis / Gabriele Centi, Fabrizio Cavani, Ferruccio Trifirò |
| Autore | CENTI, Gabriele |
| Pubbl/distr/stampa | New York [etc.] : Kluwer academic : Plenum Publishers, 2001 |
| Descrizione fisica | XIX, 505 p. : ill. ; 24 cm |
| Disciplina | 660.28443 |
| Altri autori (Persone) |
CAVANI, Fabrizio
TRIFIRO', Ferruccio |
| Soggetto topico |
Composti chimici - Ossidazione
Catalisi |
| ISBN | 0-306-46265-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNISA-990000911310203316 |
|
CENTI, Gabriele
|
||
| New York [etc.] : Kluwer academic : Plenum Publishers, 2001 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. di Salerno | ||
| ||