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Organic redox systems : synthesis, properties, and applications / / edited by Tohru Nishinaga
| Organic redox systems : synthesis, properties, and applications / / edited by Tohru Nishinaga |
| Pubbl/distr/stampa | Hoboken, New Jersey : , : Wiley, , [2016] |
| Descrizione fisica | 1 online resource (862 p.) |
| Disciplina | 547/.23 |
| Soggetto topico | Oxidation-reduction reaction |
| ISBN |
1-118-85885-9
1-118-85872-7 1-118-85898-0 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
TITLE PAGE; TABLE OF CONTENTS; LIST OF CONTRIBUTORS; PREFACE; 1 INTRODUCTION: BASIC CONCEPTS AND A BRIEF HISTORY OF ORGANIC REDOX SYSTEMS; 1.1 REDOX REACTION OF ORGANIC MOLECULES; 1.2 REDOX POTENTIAL IN NONAQUEOUS SOLVENTS; 1.3 A BRIEF HISTORY OF ORGANIC REDOX COMPOUNDS; REFERENCES; 2 REDOX-MEDIATED REVERSIBLE σ-BOND FORMATION/CLEAVAGE; 2.1 DYNAMIC REDOX ("DYREX") SYSTEMS; 2.2 ADVANCED ELECTROCHROMIC RESPONSE OF "ENDO"-TYPE DYREX SYSTEMS EXHIBITING REDOX SWITCHING OF A σ-BOND; 2.3 ADVANCED ELECTROCHROMIC RESPONSE OF "EXO"-TYPE DYREX SYSTEMS EXHIBITING REDOX SWITCHING OF A σ-BOND
2.4 PROSPECT: REDOX SYSTEMS WITH MULTIPLE DYREX UNITSREFERENCES; 3 REDOX-CONTROLLED INTRAMOLECULAR MOTIONS TRIGGERED BY π-DIMERIZATION AND PIMERIZATION PROCESSES; 3.1 INTRODUCTION; 3.2 OLIGOTHIOPHENES; 3.3 PHENOTHIAZINE; 3.4 NAPHTHALENE AND PERYLENE BISIMIDES; 3.5 para-PHENYLENEDIAMINE; 3.6 PYRIDINYL RADICALS; 3.7 VIOLOGEN DERIVATIVES; 3.8 VERDAZYL; 3.9 PHENALENYL; 3.10 PORPHYRINS; 3.11 BENZENOID; 3.12 CYCLOPHANE; 3.13 TETRATHIAFULVALENE; 3.14 CONCLUSION; ACKNOWLEDGMENTS; REFERENCES 4 TETRATHIAFULVALENE: A REDOX UNIT FOR FUNCTIONAL MATERIALS AND A BUILDING BLOCK FOR SUPRAMOLECULAR SELF-ASSEMBLY4.1 INTRODUCTION: PAST AND PRESENT OF TTF CHEMISTRY; 4.2 BASIC REDOX PROPERTIES OF TTF AND STACKED TTF; 4.3 TTF AS A FAITHFUL REDOX ACTIVE UNIT IN FUNCTIONAL MATERIALS; 4.4 ELECTROCONDUCTING PROPERTIES OF TTF DERIVATIVES BASED ON SUPRAMOLECULAR SELF-ASSEMBLY; 4.5 SUMMARY AND OUTLOOK; REFERENCES; 5 ROBUST AROMATIC CATION RADICALS AS REDOX TUNABLE OXIDANTS; 5.1 INTRODUCTION; 5.2 DESIGNING MOLECULES FOR THE FORMATION OF STABLE CATION RADICALS (CRs)-A CASE STUDY 5.3 METHODS OF PREPARATIVE ISOLATION OF AROMATIC CATION RADICALS5.4 QUANTITATIVE OXIDATION OF ELECTRON DONORS USING THE-ORANGE+· SbCl6- AS ONE-ELECTRON OXIDANT; 5.5 READILY AVAILABLE ELECTRON DONORS FOR THE REDOX-TUNABLE AROMATIC OXIDANTS; 5.6 CONCLUSION; REFERENCES; 6 AIR-STABLE REDOX-ACTIVE NEUTRAL RADICALS: TOPOLOGICAL SYMMETRY CONTROL OF ELECTRONIC-SPIN, MULTICENTERED CHEMICAL BONDING, AND ORGANIC BATTERY APPLICATION; 6.1 INTRODUCTION; 6.2 OPEN-SHELL GRAPHENE FRAGMENT: DESIGN AND SYNTHESIS OF AIR-STABLE CARBON-CENTERED NEUTRAL RADICALS BASED ON FUSED-POLYCYCLIC Π-SYSTEM 7.5 THE LENGTH OF THE BRIDGE |
| Record Nr. | UNINA-9910137222703321 |
| Hoboken, New Jersey : , : Wiley, , [2016] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Organic redox systems : synthesis, properties, and applications / / edited by Tohru Nishinaga
| Organic redox systems : synthesis, properties, and applications / / edited by Tohru Nishinaga |
| Pubbl/distr/stampa | Hoboken, New Jersey : , : Wiley, , [2016] |
| Descrizione fisica | 1 online resource (862 p.) |
| Disciplina | 547/.23 |
| Soggetto topico | Oxidation-reduction reaction |
| ISBN |
1-118-85885-9
1-118-85872-7 1-118-85898-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
TITLE PAGE; TABLE OF CONTENTS; LIST OF CONTRIBUTORS; PREFACE; 1 INTRODUCTION: BASIC CONCEPTS AND A BRIEF HISTORY OF ORGANIC REDOX SYSTEMS; 1.1 REDOX REACTION OF ORGANIC MOLECULES; 1.2 REDOX POTENTIAL IN NONAQUEOUS SOLVENTS; 1.3 A BRIEF HISTORY OF ORGANIC REDOX COMPOUNDS; REFERENCES; 2 REDOX-MEDIATED REVERSIBLE σ-BOND FORMATION/CLEAVAGE; 2.1 DYNAMIC REDOX ("DYREX") SYSTEMS; 2.2 ADVANCED ELECTROCHROMIC RESPONSE OF "ENDO"-TYPE DYREX SYSTEMS EXHIBITING REDOX SWITCHING OF A σ-BOND; 2.3 ADVANCED ELECTROCHROMIC RESPONSE OF "EXO"-TYPE DYREX SYSTEMS EXHIBITING REDOX SWITCHING OF A σ-BOND
2.4 PROSPECT: REDOX SYSTEMS WITH MULTIPLE DYREX UNITSREFERENCES; 3 REDOX-CONTROLLED INTRAMOLECULAR MOTIONS TRIGGERED BY π-DIMERIZATION AND PIMERIZATION PROCESSES; 3.1 INTRODUCTION; 3.2 OLIGOTHIOPHENES; 3.3 PHENOTHIAZINE; 3.4 NAPHTHALENE AND PERYLENE BISIMIDES; 3.5 para-PHENYLENEDIAMINE; 3.6 PYRIDINYL RADICALS; 3.7 VIOLOGEN DERIVATIVES; 3.8 VERDAZYL; 3.9 PHENALENYL; 3.10 PORPHYRINS; 3.11 BENZENOID; 3.12 CYCLOPHANE; 3.13 TETRATHIAFULVALENE; 3.14 CONCLUSION; ACKNOWLEDGMENTS; REFERENCES 4 TETRATHIAFULVALENE: A REDOX UNIT FOR FUNCTIONAL MATERIALS AND A BUILDING BLOCK FOR SUPRAMOLECULAR SELF-ASSEMBLY4.1 INTRODUCTION: PAST AND PRESENT OF TTF CHEMISTRY; 4.2 BASIC REDOX PROPERTIES OF TTF AND STACKED TTF; 4.3 TTF AS A FAITHFUL REDOX ACTIVE UNIT IN FUNCTIONAL MATERIALS; 4.4 ELECTROCONDUCTING PROPERTIES OF TTF DERIVATIVES BASED ON SUPRAMOLECULAR SELF-ASSEMBLY; 4.5 SUMMARY AND OUTLOOK; REFERENCES; 5 ROBUST AROMATIC CATION RADICALS AS REDOX TUNABLE OXIDANTS; 5.1 INTRODUCTION; 5.2 DESIGNING MOLECULES FOR THE FORMATION OF STABLE CATION RADICALS (CRs)-A CASE STUDY 5.3 METHODS OF PREPARATIVE ISOLATION OF AROMATIC CATION RADICALS5.4 QUANTITATIVE OXIDATION OF ELECTRON DONORS USING THE-ORANGE+· SbCl6- AS ONE-ELECTRON OXIDANT; 5.5 READILY AVAILABLE ELECTRON DONORS FOR THE REDOX-TUNABLE AROMATIC OXIDANTS; 5.6 CONCLUSION; REFERENCES; 6 AIR-STABLE REDOX-ACTIVE NEUTRAL RADICALS: TOPOLOGICAL SYMMETRY CONTROL OF ELECTRONIC-SPIN, MULTICENTERED CHEMICAL BONDING, AND ORGANIC BATTERY APPLICATION; 6.1 INTRODUCTION; 6.2 OPEN-SHELL GRAPHENE FRAGMENT: DESIGN AND SYNTHESIS OF AIR-STABLE CARBON-CENTERED NEUTRAL RADICALS BASED ON FUSED-POLYCYCLIC Π-SYSTEM 7.5 THE LENGTH OF THE BRIDGE |
| Record Nr. | UNINA-9910829994903321 |
| Hoboken, New Jersey : , : Wiley, , [2016] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Oxidation of amino acids, peptides, and proteins [[electronic resource] ] : kinetics and mechanism / / Virender K. Sharma
| Oxidation of amino acids, peptides, and proteins [[electronic resource] ] : kinetics and mechanism / / Virender K. Sharma |
| Autore | Sharma Virender K |
| Pubbl/distr/stampa | Hoboken, N.J., : John Wiley & Sons, c2013 |
| Descrizione fisica | 1 online resource (421 p.) |
| Disciplina | 547/.23 |
| Collana | Wiley series on reactive intermediates in chemistry and biology |
| Soggetto topico |
Oxidation-reduction reaction
Amino acids - Metabolism Pollutants Peptides - Metabolism Proteins - Metabolism |
| ISBN |
1-118-48245-X
1-118-48246-8 1-283-83528-2 1-118-48248-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Reactive species -- Acid-base properties -- Halogenated species -- Reactive oxygen species -- Reactive inorganic oxy-species of C, N, S, and P-- High-valent Cr, Mn, and Fe species. |
| Record Nr. | UNINA-9910141369303321 |
Sharma Virender K
|
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| Hoboken, N.J., : John Wiley & Sons, c2013 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Oxidation of amino acids, peptides, and proteins [[electronic resource] ] : kinetics and mechanism / / Virender K. Sharma
| Oxidation of amino acids, peptides, and proteins [[electronic resource] ] : kinetics and mechanism / / Virender K. Sharma |
| Autore | Sharma Virender K |
| Edizione | [1st ed.] |
| Pubbl/distr/stampa | Hoboken, N.J., : John Wiley & Sons, c2013 |
| Descrizione fisica | 1 online resource (421 p.) |
| Disciplina | 547/.23 |
| Collana | Wiley series on reactive intermediates in chemistry and biology |
| Soggetto topico |
Oxidation-reduction reaction
Amino acids - Metabolism Pollutants Peptides - Metabolism Proteins - Metabolism |
| ISBN |
1-118-48245-X
1-118-48246-8 1-283-83528-2 1-118-48248-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Reactive species -- Acid-base properties -- Halogenated species -- Reactive oxygen species -- Reactive inorganic oxy-species of C, N, S, and P-- High-valent Cr, Mn, and Fe species. |
| Record Nr. | UNINA-9910828786103321 |
|
Sharma Virender K
|
||
| Hoboken, N.J., : John Wiley & Sons, c2013 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Redox : Principles and Advanced Applications / / edited by Mohammed Awad Ali Khalid
| Redox : Principles and Advanced Applications / / edited by Mohammed Awad Ali Khalid |
| Pubbl/distr/stampa | Rijeka, Croatia : , : IntechOpen, , 2017 |
| Descrizione fisica | 1 online resource (250 pages) : illustrations |
| Disciplina | 541.393 |
| Soggetto topico | Oxidation-reduction reaction |
| ISBN |
953-51-4670-X
953-51-3394-2 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Altri titoli varianti | Redox |
| Record Nr. | UNINA-9910317849303321 |
| Rijeka, Croatia : , : IntechOpen, , 2017 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Redox biocatalysis [[electronic resource] ] : fundamentals and applications / / Daniela Gamenara ... [et al.]
| Redox biocatalysis [[electronic resource] ] : fundamentals and applications / / Daniela Gamenara ... [et al.] |
| Pubbl/distr/stampa | Hoboken, N.J., : Wiley, 2012 |
| Descrizione fisica | 1 online resource (549 p.) |
| Disciplina | 660.6/34 |
| Altri autori (Persone) | GamenaraDaniela <1964-> |
| Soggetto topico |
Environmental chemistry - Industrial applications
Environmental chemistry Enzymes Oxidation-reduction reaction |
| ISBN |
1-118-40932-9
1-283-64617-X 1-118-40934-5 1-118-40929-9 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
REDOX BIOCATALYSIS; CONTENTS; PREFACE; 1. Enzymes Involved in Redox Reactions: Natural Sources and Mechanistic Overview; 1.1 Motivation: Green Chemistry and Biocatalysis; 1.2 Sources of Biocatalysts; 1.2.1 Plants and Animals as Sources of Redox Biocatalysts; 1.2.2 Wild-Type Microorganisms; 1.2.2.1 Yeasts; 1.2.2.2 Fungi; 1.2.2.3 Bacteria; 1.2.3 Metagenomic Assessments; 1.3 Overview of Redox Enzymes; 1.3.1 Dehydrogenases; 1.3.1.1 Zn-Dependent Dehydrogenases; 1.3.1.2 Flavin-Dependent Dehydrogenases; 1.3.1.3 Pterin-Dependent Dehydrogenases; 1.3.1.4 Quinoprotein Dehydrogenases
1.3.1.5 Dehydrogenases without Prosthetic Group1.3.2 Oxygenases; 1.3.2.1 Monooxygenases; 1.3.2.2 Dioxygenases; 1.3.3 Oxidases; 1.3.3.1 Iron-Containing Oxidases; 1.3.3.2 Copper-Containing Oxidases; 1.3.3.3 Flavin-Dependent Oxidases; 1.3.4 Peroxidases; 1.4 Concluding Remarks; References; 2. Natural Cofactors and Their Regeneration Strategies; 2.1 Types of Natural Cofactors-Mechanisms; 2.2 Cofactor Regeneration; 2.2.1 Enzymatic Regeneration of Reduced Cofactors; 2.2.1.1 Substrate-Assisted Method; 2.2.1.2 Enzyme-Assisted Method; 2.2.2 Enzymatic Regeneration of Oxidized Cofactors 2.2.3 Chemical Regeneration of Cofactors2.2.4 Electrochemical Regeneration of Cofactors; 2.2.5 Photochemical Regeneration of Cofactors; 2.3 Concluding Remarks; References; 3. Reactions Involving Dehydrogenases; 3.1 General Considerations; 3.2 Reduction of Carbonyl Groups; 3.2.1 Reduction of Aliphatic and Aromatic Ketones; 3.2.2 Reduction of α- and β-keto Esters and Derivatives; 3.2.3 Reduction of Diketones; 3.2.4 Reduction of Aldehydes; 3.3 Racemization and Deracemization Reactions; 3.4 Preparation of Amines; 3.5 Reduction of C-C Double Bonds; 3.6 Oxidation Reactions 3.7 Dehydrogenase-Catalyzed Redox Reactions in Natural Products3.8 Concluding Remarks; References; 4. Reactions Involving Oxygenases; 4.1 Monooxygenase-Catalyzed Reactions; 4.1.1 Hydroxylation of Aliphatic Compounds; 4.1.2 Hydroxylation of Aromatic Compounds; 4.1.3 Baeyer-Villiger Reactions; 4.1.3.1 Classification and Metabolic Role of BVMOs; 4.1.3.2 Isolated Enzymes versus Whole-Cell Systems (Wild-Type and Recombinant Microorganisms); 4.1.3.3 Substrate Profile of Available Baeyer-Villiger Monooxygenases; 4.1.3.4 Synthetic Applications of BVMOs; 4.1.4 Epoxidation of Alkenes 4.2 Dioxygenase-Catalyzed Reactions4.2.1 Aromatic Dioxygenases; 4.2.1.1 Dihydroxylation of Aromatic Compounds; 4.2.1.2 Other Oxidation Reactions Performed by Aromatic Dioxygenases; 4.2.2 Miscellaneous Dioxygenases; 4.2.2.1 Lipoxygenase; 4.3 Concluding Remarks; References; 5. Reactions Involving Oxidases and Peroxidases; 5.1 Oxidase-Catalyzed Reactions; 5.1.1 Oxidases Acting on C-O Bonds; 5.1.1.1 Galactose Oxidase; 5.1.1.2 Pyranose Oxidase; 5.1.1.3 Alcohol Oxidase; 5.1.1.4 Glucose Oxidase; 5.1.1.5 Glycolate Oxidase; 5.1.2 Laccases and Tyrosinases (Phenol Oxidases); 5.1.2.1 Laccase 5.1.2.2 Tyrosinase and Other Polyphenol Oxidases |
| Record Nr. | UNINA-9910141395103321 |
| Hoboken, N.J., : Wiley, 2012 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Redox biocatalysis [[electronic resource] ] : fundamentals and applications / / Daniela Gamenara ... [et al.]
| Redox biocatalysis [[electronic resource] ] : fundamentals and applications / / Daniela Gamenara ... [et al.] |
| Edizione | [1st ed.] |
| Pubbl/distr/stampa | Hoboken, N.J., : Wiley, 2012 |
| Descrizione fisica | 1 online resource (549 p.) |
| Disciplina | 660.6/34 |
| Altri autori (Persone) | GamenaraDaniela <1964-> |
| Soggetto topico |
Environmental chemistry - Industrial applications
Environmental chemistry Enzymes Oxidation-reduction reaction |
| ISBN |
1-118-40932-9
1-283-64617-X 1-118-40934-5 1-118-40929-9 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
REDOX BIOCATALYSIS; CONTENTS; PREFACE; 1. Enzymes Involved in Redox Reactions: Natural Sources and Mechanistic Overview; 1.1 Motivation: Green Chemistry and Biocatalysis; 1.2 Sources of Biocatalysts; 1.2.1 Plants and Animals as Sources of Redox Biocatalysts; 1.2.2 Wild-Type Microorganisms; 1.2.2.1 Yeasts; 1.2.2.2 Fungi; 1.2.2.3 Bacteria; 1.2.3 Metagenomic Assessments; 1.3 Overview of Redox Enzymes; 1.3.1 Dehydrogenases; 1.3.1.1 Zn-Dependent Dehydrogenases; 1.3.1.2 Flavin-Dependent Dehydrogenases; 1.3.1.3 Pterin-Dependent Dehydrogenases; 1.3.1.4 Quinoprotein Dehydrogenases
1.3.1.5 Dehydrogenases without Prosthetic Group1.3.2 Oxygenases; 1.3.2.1 Monooxygenases; 1.3.2.2 Dioxygenases; 1.3.3 Oxidases; 1.3.3.1 Iron-Containing Oxidases; 1.3.3.2 Copper-Containing Oxidases; 1.3.3.3 Flavin-Dependent Oxidases; 1.3.4 Peroxidases; 1.4 Concluding Remarks; References; 2. Natural Cofactors and Their Regeneration Strategies; 2.1 Types of Natural Cofactors-Mechanisms; 2.2 Cofactor Regeneration; 2.2.1 Enzymatic Regeneration of Reduced Cofactors; 2.2.1.1 Substrate-Assisted Method; 2.2.1.2 Enzyme-Assisted Method; 2.2.2 Enzymatic Regeneration of Oxidized Cofactors 2.2.3 Chemical Regeneration of Cofactors2.2.4 Electrochemical Regeneration of Cofactors; 2.2.5 Photochemical Regeneration of Cofactors; 2.3 Concluding Remarks; References; 3. Reactions Involving Dehydrogenases; 3.1 General Considerations; 3.2 Reduction of Carbonyl Groups; 3.2.1 Reduction of Aliphatic and Aromatic Ketones; 3.2.2 Reduction of α- and β-keto Esters and Derivatives; 3.2.3 Reduction of Diketones; 3.2.4 Reduction of Aldehydes; 3.3 Racemization and Deracemization Reactions; 3.4 Preparation of Amines; 3.5 Reduction of C-C Double Bonds; 3.6 Oxidation Reactions 3.7 Dehydrogenase-Catalyzed Redox Reactions in Natural Products3.8 Concluding Remarks; References; 4. Reactions Involving Oxygenases; 4.1 Monooxygenase-Catalyzed Reactions; 4.1.1 Hydroxylation of Aliphatic Compounds; 4.1.2 Hydroxylation of Aromatic Compounds; 4.1.3 Baeyer-Villiger Reactions; 4.1.3.1 Classification and Metabolic Role of BVMOs; 4.1.3.2 Isolated Enzymes versus Whole-Cell Systems (Wild-Type and Recombinant Microorganisms); 4.1.3.3 Substrate Profile of Available Baeyer-Villiger Monooxygenases; 4.1.3.4 Synthetic Applications of BVMOs; 4.1.4 Epoxidation of Alkenes 4.2 Dioxygenase-Catalyzed Reactions4.2.1 Aromatic Dioxygenases; 4.2.1.1 Dihydroxylation of Aromatic Compounds; 4.2.1.2 Other Oxidation Reactions Performed by Aromatic Dioxygenases; 4.2.2 Miscellaneous Dioxygenases; 4.2.2.1 Lipoxygenase; 4.3 Concluding Remarks; References; 5. Reactions Involving Oxidases and Peroxidases; 5.1 Oxidase-Catalyzed Reactions; 5.1.1 Oxidases Acting on C-O Bonds; 5.1.1.1 Galactose Oxidase; 5.1.1.2 Pyranose Oxidase; 5.1.1.3 Alcohol Oxidase; 5.1.1.4 Glucose Oxidase; 5.1.1.5 Glycolate Oxidase; 5.1.2 Laccases and Tyrosinases (Phenol Oxidases); 5.1.2.1 Laccase 5.1.2.2 Tyrosinase and Other Polyphenol Oxidases |
| Record Nr. | UNINA-9910828619203321 |
| Hoboken, N.J., : Wiley, 2012 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Redox biochemistry and chemistry
| Redox biochemistry and chemistry |
| Pubbl/distr/stampa | [London] : , : Elsevier Ltd., , [2023]- |
| Descrizione fisica | 1 online resource |
| Soggetto topico |
Oxidation-reduction reaction
Oxidation-reduction reaction - Physiological effect Biochemistry Oxydoréduction Oxydoréduction - Effets physiologiques Biochimie biochemistry Oxidation-Reduction Chemical Phenomena |
| Soggetto genere / forma |
Periodicals
Periodical |
| ISSN | 2773-1766 |
| Formato | Materiale a stampa |
| Livello bibliografico | Periodico |
| Lingua di pubblicazione | eng |
| Altri titoli varianti | RBC |
| Record Nr. | UNINA-9910595452303321 |
| [London] : , : Elsevier Ltd., , [2023]- | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Redox chemistry : from molecules to energy storage / / edited by Olivier Fontaine
| Redox chemistry : from molecules to energy storage / / edited by Olivier Fontaine |
| Pubbl/distr/stampa | London : , : IntechOpen, , 2022 |
| Descrizione fisica | 1 online resource (94 pages) |
| Disciplina | 541.393 |
| Soggetto topico |
Oxidation-reduction reaction
Oxidation-reduction reaction - Programmed instruction |
| ISBN | 1-80355-538-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | 1. Introductory Chapter: Molecules and Materials Associated with Redox Reactions -- 2. Redox Mediated Electrolytes in Electrochemical Capacitors -- 3. Redox Transitions in Pseudocapacitor Materials: Criteria and Ruling Factors -- 4. Effects of Electrolyte on Redox Potentials -- 5. Charge Carriers for Next-Generation Redox Flow Batteries. |
| Altri titoli varianti | Redox Chemistry |
| Record Nr. | UNINA-9910633964303321 |
| London : , : IntechOpen, , 2022 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Redox Chemistry : from molecules to energy storage / / editor, Olivier Fontaine
| Redox Chemistry : from molecules to energy storage / / editor, Olivier Fontaine |
| Pubbl/distr/stampa | London : , : IntechOpen, , 2022 |
| Descrizione fisica | 1 online resource (ix, 69 pages) |
| Disciplina | 541.393 |
| Soggetto topico | Oxidation-reduction reaction |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | 1. Introductory Chapter: Molecules and Materials Associated with Redox Reactions -- 2. Redox Mediated Electrolytes in Electrochemical Capacitors -- 3. Redox Transitions in Pseudocapacitor Materials: Criteria and Ruling Factors -- 4. Effects of Electrolyte on Redox Potentials -- 5. Charge Carriers for Next-Generation Redox Flow Batteries. |
| Record Nr. | UNINA-9910688147603321 |
| London : , : IntechOpen, , 2022 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
