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Electron-transfer and electrochemical reactions [[electronic resource] ] : photochemical and other energized reactions / / editor, J.J. Zuckerman; subject index editor, A.P. Hagen
Electron-transfer and electrochemical reactions [[electronic resource] ] : photochemical and other energized reactions / / editor, J.J. Zuckerman; subject index editor, A.P. Hagen
Pubbl/distr/stampa [Deerfield Beach, FL], : VCH, c1986
Descrizione fisica 1 online resource (426 p.)
Disciplina 541.3/9
541.39
Altri autori (Persone) ZuckermanJ. J <1936-1987.> (Jerold J.)
Collana Inorganic reactions and methods
Soggetto topico Photochemistry
Charge transfer
Soggetto genere / forma Electronic books.
ISBN 1-282-30827-0
9786612308277
0-470-14530-7
0-470-14551-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Inorganic Reactions and Methods; Contents; How to Use this Book; Preface to the Series; Editorial Consultants to the Series; Contributors to Volume 15; Electron-Transfer and Electrochemical Reactions; Introduction; Electron Transfer; Introduction; Classification of Electron-Transfer Reactions; Outer-Sphere Reactions; Examples of Outer-Sphere Reactions; Outer-Sphere Transition States; Inner-Sphere Reactions; Inner-Sphere Reactions: Scheme I; Inner-Sphere Reactions: Scheme II; Inner-Sphere Reactions: Scheme Ill; Double-Ligand Bridging; Other Reaction Classes
Mixed Outer- and Innersphere ReactionsIntramolecular Electron Transfer; Two-Electron Transfers; Theory of Electron-Transfer Reactions; The Stability of the Precursor Complex; Potential-Energy Surfaces; of Zero Order.; of First Order.; The Electronic Factor; Electron-Exchange Reactions; The Reorganization Energy; Nuclear Tunneling in Electron Exchange; Quantum-Mechanical Treatment; Comparison of Observed and Calculated Parameters for Electron Exchange; Electron Transfer Accompanied by a Net Chemical Change; Semiclassical Treatment; Cross Reactions and Electron-Exchange Rates
Quantum-Mechanical TreatmentConclusions; General Reactivity Patterns in Electron Transfer; The Inner-Shell Reorganization Energy: Exchange Rates of Aquo Ions; Variations with Ligand: The Outer-Shell Reorganization Energy; Electronic Factors: Nonadiabaticity; Free-Energy Relations; Inner-Sphere Versus Outer-Sphere Electron Transfer; Rate Saturation in Electron Transfer; Specific Reactivity Patterns in Electron-Transfer Reactions; Variation with the Reductant; One-Electron Reductants; Two-Electron Reductants; Variation with the Oxidant; One-Electron Oxidants; Multiple-Electron Oxidants
Oxidation and Reduction of Coordinated LigandsCatalysis in Electron-Transfer Reactions; Catalyzed Electron Transfer; Catalyzed Ligand Substitution; Induced Electron-Transfer Reactions; Photoinduced Electron-Transfer Reactions; Electrochemical Reactions; Introduction; The Electrode Process; Reversibility; Electrochemical Reversibility; Chemical Reversibility; Complex Electrode Mechanisms; Diagnostic Electrochemical Measurements; Voltammetric Methods; Direct-Current Polarography; Pulse-Polarographic Methods; Alternating-Current Polarography; Cyclic Voltammetry; Evaluation of Formal Potentials
Involving Stable Reactants and Products.Involving Unstable Electrode Products.; Involving Reactants Undergoing Multiple- Electrode Reactions.; Chemical Reactions Accompanying Electrode Reactions; Reactions Preceding Electron Transfer (CE); Slow-Reaction (1 >a) Limit; Intermediate-Reaction Kinetics; Reactions Following Electron Transfer (EC); Giving Electroinactive Products.; Giving Electroactive Products (ECE).; Other Coupled Chemical Reactions; Electrochemical Synthesis; by Controlled-Potential Electrolysis.; Involving Bulk Preparations.; Conclusions
Thermodynamics of Simple Electrochemical Reactions
Record Nr. UNINA-9910144319203321
[Deerfield Beach, FL], : VCH, c1986
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Electron-transfer and electrochemical reactions [[electronic resource] ] : photochemical and other energized reactions / / editor, J.J. Zuckerman; subject index editor, A.P. Hagen
Electron-transfer and electrochemical reactions [[electronic resource] ] : photochemical and other energized reactions / / editor, J.J. Zuckerman; subject index editor, A.P. Hagen
Pubbl/distr/stampa [Deerfield Beach, FL], : VCH, c1986
Descrizione fisica 1 online resource (426 p.)
Disciplina 541.3/9
541.39
Altri autori (Persone) ZuckermanJ. J <1936-1987.> (Jerold J.)
Collana Inorganic reactions and methods
Soggetto topico Photochemistry
Charge transfer
ISBN 1-282-30827-0
9786612308277
0-470-14530-7
0-470-14551-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Inorganic Reactions and Methods; Contents; How to Use this Book; Preface to the Series; Editorial Consultants to the Series; Contributors to Volume 15; Electron-Transfer and Electrochemical Reactions; Introduction; Electron Transfer; Introduction; Classification of Electron-Transfer Reactions; Outer-Sphere Reactions; Examples of Outer-Sphere Reactions; Outer-Sphere Transition States; Inner-Sphere Reactions; Inner-Sphere Reactions: Scheme I; Inner-Sphere Reactions: Scheme II; Inner-Sphere Reactions: Scheme Ill; Double-Ligand Bridging; Other Reaction Classes
Mixed Outer- and Innersphere ReactionsIntramolecular Electron Transfer; Two-Electron Transfers; Theory of Electron-Transfer Reactions; The Stability of the Precursor Complex; Potential-Energy Surfaces; of Zero Order.; of First Order.; The Electronic Factor; Electron-Exchange Reactions; The Reorganization Energy; Nuclear Tunneling in Electron Exchange; Quantum-Mechanical Treatment; Comparison of Observed and Calculated Parameters for Electron Exchange; Electron Transfer Accompanied by a Net Chemical Change; Semiclassical Treatment; Cross Reactions and Electron-Exchange Rates
Quantum-Mechanical TreatmentConclusions; General Reactivity Patterns in Electron Transfer; The Inner-Shell Reorganization Energy: Exchange Rates of Aquo Ions; Variations with Ligand: The Outer-Shell Reorganization Energy; Electronic Factors: Nonadiabaticity; Free-Energy Relations; Inner-Sphere Versus Outer-Sphere Electron Transfer; Rate Saturation in Electron Transfer; Specific Reactivity Patterns in Electron-Transfer Reactions; Variation with the Reductant; One-Electron Reductants; Two-Electron Reductants; Variation with the Oxidant; One-Electron Oxidants; Multiple-Electron Oxidants
Oxidation and Reduction of Coordinated LigandsCatalysis in Electron-Transfer Reactions; Catalyzed Electron Transfer; Catalyzed Ligand Substitution; Induced Electron-Transfer Reactions; Photoinduced Electron-Transfer Reactions; Electrochemical Reactions; Introduction; The Electrode Process; Reversibility; Electrochemical Reversibility; Chemical Reversibility; Complex Electrode Mechanisms; Diagnostic Electrochemical Measurements; Voltammetric Methods; Direct-Current Polarography; Pulse-Polarographic Methods; Alternating-Current Polarography; Cyclic Voltammetry; Evaluation of Formal Potentials
Involving Stable Reactants and Products.Involving Unstable Electrode Products.; Involving Reactants Undergoing Multiple- Electrode Reactions.; Chemical Reactions Accompanying Electrode Reactions; Reactions Preceding Electron Transfer (CE); Slow-Reaction (1 >a) Limit; Intermediate-Reaction Kinetics; Reactions Following Electron Transfer (EC); Giving Electroinactive Products.; Giving Electroactive Products (ECE).; Other Coupled Chemical Reactions; Electrochemical Synthesis; by Controlled-Potential Electrolysis.; Involving Bulk Preparations.; Conclusions
Thermodynamics of Simple Electrochemical Reactions
Record Nr. UNINA-9910643494803321
[Deerfield Beach, FL], : VCH, c1986
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Electron-transfer and electrochemical reactions [[electronic resource] ] : photochemical and other energized reactions / / editor, J.J. Zuckerman; subject index editor, A.P. Hagen
Electron-transfer and electrochemical reactions [[electronic resource] ] : photochemical and other energized reactions / / editor, J.J. Zuckerman; subject index editor, A.P. Hagen
Pubbl/distr/stampa [Deerfield Beach, FL], : VCH, c1986
Descrizione fisica 1 online resource (426 p.)
Disciplina 541.3/9
541.39
Altri autori (Persone) ZuckermanJ. J <1936-1987.> (Jerold J.)
Collana Inorganic reactions and methods
Soggetto topico Photochemistry
Charge transfer
ISBN 1-282-30827-0
9786612308277
0-470-14530-7
0-470-14551-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Inorganic Reactions and Methods; Contents; How to Use this Book; Preface to the Series; Editorial Consultants to the Series; Contributors to Volume 15; Electron-Transfer and Electrochemical Reactions; Introduction; Electron Transfer; Introduction; Classification of Electron-Transfer Reactions; Outer-Sphere Reactions; Examples of Outer-Sphere Reactions; Outer-Sphere Transition States; Inner-Sphere Reactions; Inner-Sphere Reactions: Scheme I; Inner-Sphere Reactions: Scheme II; Inner-Sphere Reactions: Scheme Ill; Double-Ligand Bridging; Other Reaction Classes
Mixed Outer- and Innersphere ReactionsIntramolecular Electron Transfer; Two-Electron Transfers; Theory of Electron-Transfer Reactions; The Stability of the Precursor Complex; Potential-Energy Surfaces; of Zero Order.; of First Order.; The Electronic Factor; Electron-Exchange Reactions; The Reorganization Energy; Nuclear Tunneling in Electron Exchange; Quantum-Mechanical Treatment; Comparison of Observed and Calculated Parameters for Electron Exchange; Electron Transfer Accompanied by a Net Chemical Change; Semiclassical Treatment; Cross Reactions and Electron-Exchange Rates
Quantum-Mechanical TreatmentConclusions; General Reactivity Patterns in Electron Transfer; The Inner-Shell Reorganization Energy: Exchange Rates of Aquo Ions; Variations with Ligand: The Outer-Shell Reorganization Energy; Electronic Factors: Nonadiabaticity; Free-Energy Relations; Inner-Sphere Versus Outer-Sphere Electron Transfer; Rate Saturation in Electron Transfer; Specific Reactivity Patterns in Electron-Transfer Reactions; Variation with the Reductant; One-Electron Reductants; Two-Electron Reductants; Variation with the Oxidant; One-Electron Oxidants; Multiple-Electron Oxidants
Oxidation and Reduction of Coordinated LigandsCatalysis in Electron-Transfer Reactions; Catalyzed Electron Transfer; Catalyzed Ligand Substitution; Induced Electron-Transfer Reactions; Photoinduced Electron-Transfer Reactions; Electrochemical Reactions; Introduction; The Electrode Process; Reversibility; Electrochemical Reversibility; Chemical Reversibility; Complex Electrode Mechanisms; Diagnostic Electrochemical Measurements; Voltammetric Methods; Direct-Current Polarography; Pulse-Polarographic Methods; Alternating-Current Polarography; Cyclic Voltammetry; Evaluation of Formal Potentials
Involving Stable Reactants and Products.Involving Unstable Electrode Products.; Involving Reactants Undergoing Multiple- Electrode Reactions.; Chemical Reactions Accompanying Electrode Reactions; Reactions Preceding Electron Transfer (CE); Slow-Reaction (1 >a) Limit; Intermediate-Reaction Kinetics; Reactions Following Electron Transfer (EC); Giving Electroinactive Products.; Giving Electroactive Products (ECE).; Other Coupled Chemical Reactions; Electrochemical Synthesis; by Controlled-Potential Electrolysis.; Involving Bulk Preparations.; Conclusions
Thermodynamics of Simple Electrochemical Reactions
Record Nr. UNISA-996211961703316
[Deerfield Beach, FL], : VCH, c1986
Materiale a stampa
Lo trovi qui: Univ. di Salerno
Opac: Controlla la disponibilità qui
Electron-transfer and electrochemical reactions [[electronic resource] ] : photochemical and other energized reactions / / editor, J.J. Zuckerman; subject index editor, A.P. Hagen
Electron-transfer and electrochemical reactions [[electronic resource] ] : photochemical and other energized reactions / / editor, J.J. Zuckerman; subject index editor, A.P. Hagen
Pubbl/distr/stampa [Deerfield Beach, FL], : VCH, c1986
Descrizione fisica 1 online resource (426 p.)
Disciplina 541.3/9
541.39
Altri autori (Persone) ZuckermanJ. J <1936-1987.> (Jerold J.)
Collana Inorganic reactions and methods
Soggetto topico Photochemistry
Charge transfer
ISBN 1-282-30827-0
9786612308277
0-470-14530-7
0-470-14551-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Inorganic Reactions and Methods; Contents; How to Use this Book; Preface to the Series; Editorial Consultants to the Series; Contributors to Volume 15; Electron-Transfer and Electrochemical Reactions; Introduction; Electron Transfer; Introduction; Classification of Electron-Transfer Reactions; Outer-Sphere Reactions; Examples of Outer-Sphere Reactions; Outer-Sphere Transition States; Inner-Sphere Reactions; Inner-Sphere Reactions: Scheme I; Inner-Sphere Reactions: Scheme II; Inner-Sphere Reactions: Scheme Ill; Double-Ligand Bridging; Other Reaction Classes
Mixed Outer- and Innersphere ReactionsIntramolecular Electron Transfer; Two-Electron Transfers; Theory of Electron-Transfer Reactions; The Stability of the Precursor Complex; Potential-Energy Surfaces; of Zero Order.; of First Order.; The Electronic Factor; Electron-Exchange Reactions; The Reorganization Energy; Nuclear Tunneling in Electron Exchange; Quantum-Mechanical Treatment; Comparison of Observed and Calculated Parameters for Electron Exchange; Electron Transfer Accompanied by a Net Chemical Change; Semiclassical Treatment; Cross Reactions and Electron-Exchange Rates
Quantum-Mechanical TreatmentConclusions; General Reactivity Patterns in Electron Transfer; The Inner-Shell Reorganization Energy: Exchange Rates of Aquo Ions; Variations with Ligand: The Outer-Shell Reorganization Energy; Electronic Factors: Nonadiabaticity; Free-Energy Relations; Inner-Sphere Versus Outer-Sphere Electron Transfer; Rate Saturation in Electron Transfer; Specific Reactivity Patterns in Electron-Transfer Reactions; Variation with the Reductant; One-Electron Reductants; Two-Electron Reductants; Variation with the Oxidant; One-Electron Oxidants; Multiple-Electron Oxidants
Oxidation and Reduction of Coordinated LigandsCatalysis in Electron-Transfer Reactions; Catalyzed Electron Transfer; Catalyzed Ligand Substitution; Induced Electron-Transfer Reactions; Photoinduced Electron-Transfer Reactions; Electrochemical Reactions; Introduction; The Electrode Process; Reversibility; Electrochemical Reversibility; Chemical Reversibility; Complex Electrode Mechanisms; Diagnostic Electrochemical Measurements; Voltammetric Methods; Direct-Current Polarography; Pulse-Polarographic Methods; Alternating-Current Polarography; Cyclic Voltammetry; Evaluation of Formal Potentials
Involving Stable Reactants and Products.Involving Unstable Electrode Products.; Involving Reactants Undergoing Multiple- Electrode Reactions.; Chemical Reactions Accompanying Electrode Reactions; Reactions Preceding Electron Transfer (CE); Slow-Reaction (1 >a) Limit; Intermediate-Reaction Kinetics; Reactions Following Electron Transfer (EC); Giving Electroinactive Products.; Giving Electroactive Products (ECE).; Other Coupled Chemical Reactions; Electrochemical Synthesis; by Controlled-Potential Electrolysis.; Involving Bulk Preparations.; Conclusions
Thermodynamics of Simple Electrochemical Reactions
Record Nr. UNINA-9910830302303321
[Deerfield Beach, FL], : VCH, c1986
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Electron-transfer and electrochemical reactions : photochemical and other energized reactions / / editor, J.J. Zuckerman; subject index editor, A.P. Hagen
Electron-transfer and electrochemical reactions : photochemical and other energized reactions / / editor, J.J. Zuckerman; subject index editor, A.P. Hagen
Pubbl/distr/stampa [Deerfield Beach, FL], : VCH, c1986
Descrizione fisica 1 online resource (426 p.)
Disciplina 541.3/9
541.39
Altri autori (Persone) ZuckermanJ. J <1936-1987.> (Jerold J.)
Collana Inorganic reactions and methods
Soggetto topico Photochemistry
Charge transfer
ISBN 1-282-30827-0
9786612308277
0-470-14530-7
0-470-14551-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Inorganic Reactions and Methods; Contents; How to Use this Book; Preface to the Series; Editorial Consultants to the Series; Contributors to Volume 15; Electron-Transfer and Electrochemical Reactions; Introduction; Electron Transfer; Introduction; Classification of Electron-Transfer Reactions; Outer-Sphere Reactions; Examples of Outer-Sphere Reactions; Outer-Sphere Transition States; Inner-Sphere Reactions; Inner-Sphere Reactions: Scheme I; Inner-Sphere Reactions: Scheme II; Inner-Sphere Reactions: Scheme Ill; Double-Ligand Bridging; Other Reaction Classes
Mixed Outer- and Innersphere ReactionsIntramolecular Electron Transfer; Two-Electron Transfers; Theory of Electron-Transfer Reactions; The Stability of the Precursor Complex; Potential-Energy Surfaces; of Zero Order.; of First Order.; The Electronic Factor; Electron-Exchange Reactions; The Reorganization Energy; Nuclear Tunneling in Electron Exchange; Quantum-Mechanical Treatment; Comparison of Observed and Calculated Parameters for Electron Exchange; Electron Transfer Accompanied by a Net Chemical Change; Semiclassical Treatment; Cross Reactions and Electron-Exchange Rates
Quantum-Mechanical TreatmentConclusions; General Reactivity Patterns in Electron Transfer; The Inner-Shell Reorganization Energy: Exchange Rates of Aquo Ions; Variations with Ligand: The Outer-Shell Reorganization Energy; Electronic Factors: Nonadiabaticity; Free-Energy Relations; Inner-Sphere Versus Outer-Sphere Electron Transfer; Rate Saturation in Electron Transfer; Specific Reactivity Patterns in Electron-Transfer Reactions; Variation with the Reductant; One-Electron Reductants; Two-Electron Reductants; Variation with the Oxidant; One-Electron Oxidants; Multiple-Electron Oxidants
Oxidation and Reduction of Coordinated LigandsCatalysis in Electron-Transfer Reactions; Catalyzed Electron Transfer; Catalyzed Ligand Substitution; Induced Electron-Transfer Reactions; Photoinduced Electron-Transfer Reactions; Electrochemical Reactions; Introduction; The Electrode Process; Reversibility; Electrochemical Reversibility; Chemical Reversibility; Complex Electrode Mechanisms; Diagnostic Electrochemical Measurements; Voltammetric Methods; Direct-Current Polarography; Pulse-Polarographic Methods; Alternating-Current Polarography; Cyclic Voltammetry; Evaluation of Formal Potentials
Involving Stable Reactants and Products.Involving Unstable Electrode Products.; Involving Reactants Undergoing Multiple- Electrode Reactions.; Chemical Reactions Accompanying Electrode Reactions; Reactions Preceding Electron Transfer (CE); Slow-Reaction (1 >a) Limit; Intermediate-Reaction Kinetics; Reactions Following Electron Transfer (EC); Giving Electroinactive Products.; Giving Electroactive Products (ECE).; Other Coupled Chemical Reactions; Electrochemical Synthesis; by Controlled-Potential Electrolysis.; Involving Bulk Preparations.; Conclusions
Thermodynamics of Simple Electrochemical Reactions
Record Nr. UNINA-9910877143303321
[Deerfield Beach, FL], : VCH, c1986
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Formation of bonds to C, Si, Ge, Sn, Pb . Part 1 [[electronic resource] /] / founding editor, J.J. Zuckerman; editor, A.P. Hagen
Formation of bonds to C, Si, Ge, Sn, Pb . Part 1 [[electronic resource] /] / founding editor, J.J. Zuckerman; editor, A.P. Hagen
Pubbl/distr/stampa New York, N.Y., : VCH Publishers, 1991
Descrizione fisica 1 online resource (633 p.)
Disciplina 541.3/9
541.39
Altri autori (Persone) ZuckermanJ. J <1936-1987.> (Jerold J.)
HagenA. P
Collana Inorganic reactions and methods
Soggetto topico Chemical kinetics - Effect of temperature on
Inorganic compounds - Synthesis
Soggetto genere / forma Electronic books.
ISBN 1-282-30813-0
9786612308130
0-470-14523-4
0-470-14544-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Inorganic Reactions and Methods; Contents; How to use this book; Preface to the Series; Editorial Consultants to the Series; Contributors to Volume 9; Formation of the Bonds to the Group-IVB (C, Si, Ge, Sn, Pb) Elements; Introduction; Formation of the Group-IVB (C, Si, Ge, Sn, Pb)-Group-IVB (C, Si, Ge, Sn, Pb) Element Bond; Introduction; Formation of the Carbon-Carbon Bond; Formation of the Si-Si Bond; in Elemental Silicon; from Oxides.; by Other Methods.; Formation of High-Purity Silicon; Electrochemical Formation of Compounds with Si-Si Bonds (Including Elemental Silicon)
from Metal Silicidesby Solvolysis in Aqueous or Liquid Ammonia Solutions.; Formation of Oligosilanes; Formation of Polymeric Compounds; from Silicon Hydrides and Organosilicon Hydrides; by the Action of a Silent Electric Discharge.; by Direct Photolysis.; by Sensitized Photolysis.; by Catalyzed Reactions.; by Reaction with Silylmetallic Compounds.; from Silicon Halides and Organosilicon Halides; by Electrochemical Reduction.; by Halide Elimination with Active Metals.; by Reaction with Silylmetallics.; by Catalyzed Disproportionation.; by Reaction with Organomagnesium Halide Reagents.
by the Action of Silent Electric Discharge.by Mercury-Photosensitized Photolyses.; from Bissilylmercury Compounds; by Thermolysis.; by Photolysis.; from Organosilanes and Silicon Halides by Hydrogenolysis.; from Silylenes; by Oligomerization.; by Insertions into Bonds of Silicon to Hydrogen, Oxygen and Silicon.; by Addition to Si = C.; in the Direct Reaction of Methyl Chloride with Silicon-Copper.; Formation of the Germanium-Germanium Bond; in Elemental Germanium; from Oxides.; from Sulfides.; by Other Syntheses.; Formation of High-Purity Germanium.; from Organogermanium Hydrides
by Reaction with Diorganomercury Compounds in the Presence of UV Radiation.by Hydrogermolysis Reaction.; by Germanium Hydride Decomposition.; from Ge(lV) Halides and Organogermanium(IV) Halides; by the Action of a Microwave Discharge of Ge(lV) Halides.; by Electrochemical Reduction.; by Halide Elimination with Active Metals.; by Reaction with Germyl-Metal Reagents.; by Reaction with Organometallic Reagents.; from Germanium(lI) Halides; by Reactions with Germyl-Metal Reagents.; by Reaction with Organometallic Reagents.; from Germyl Compounds of Cadmium, Mercury, Thallium, Antimony and Bismuth
by Thermolysis or Photolysis.from Germylenes; by Oligomerization of Germylenes.; by Insertions into Bonds of Germanium to Hydrogen, Halogen, Carbon, Oxygen, Sulfur, Nitrogen, Phosphorus and Germanium.; The Formation of the Tin-Tin Bond; in Elemental Tin; from Oxides.; from Sulfides.; by Other Syntheses.; Allotropy of Tin; from Organotin Hydrides; by Catalytic Hydrogen Elimination.; by Reaction with Organotin Halogen, Pseudohalogen, Chalcogen and Pnictogen Compounds.; by Reaction with Organometallic Compounds.; by Reaction with Reducible Organic Compounds.; from Organotin Halides
by Electrochemical Reduction.
Record Nr. UNINA-9910144322603321
New York, N.Y., : VCH Publishers, 1991
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Formation of bonds to C, Si, Ge, Sn, Pb . Part 1 [[electronic resource] /] / founding editor, J.J. Zuckerman; editor, A.P. Hagen
Formation of bonds to C, Si, Ge, Sn, Pb . Part 1 [[electronic resource] /] / founding editor, J.J. Zuckerman; editor, A.P. Hagen
Pubbl/distr/stampa New York, N.Y., : VCH Publishers, 1991
Descrizione fisica 1 online resource (633 p.)
Disciplina 541.3/9
541.39
Altri autori (Persone) ZuckermanJ. J <1936-1987.> (Jerold J.)
HagenA. P
Collana Inorganic reactions and methods
Soggetto topico Chemical kinetics - Effect of temperature on
Inorganic compounds - Synthesis
ISBN 1-282-30813-0
9786612308130
0-470-14523-4
0-470-14544-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Inorganic Reactions and Methods; Contents; How to use this book; Preface to the Series; Editorial Consultants to the Series; Contributors to Volume 9; Formation of the Bonds to the Group-IVB (C, Si, Ge, Sn, Pb) Elements; Introduction; Formation of the Group-IVB (C, Si, Ge, Sn, Pb)-Group-IVB (C, Si, Ge, Sn, Pb) Element Bond; Introduction; Formation of the Carbon-Carbon Bond; Formation of the Si-Si Bond; in Elemental Silicon; from Oxides.; by Other Methods.; Formation of High-Purity Silicon; Electrochemical Formation of Compounds with Si-Si Bonds (Including Elemental Silicon)
from Metal Silicidesby Solvolysis in Aqueous or Liquid Ammonia Solutions.; Formation of Oligosilanes; Formation of Polymeric Compounds; from Silicon Hydrides and Organosilicon Hydrides; by the Action of a Silent Electric Discharge.; by Direct Photolysis.; by Sensitized Photolysis.; by Catalyzed Reactions.; by Reaction with Silylmetallic Compounds.; from Silicon Halides and Organosilicon Halides; by Electrochemical Reduction.; by Halide Elimination with Active Metals.; by Reaction with Silylmetallics.; by Catalyzed Disproportionation.; by Reaction with Organomagnesium Halide Reagents.
by the Action of Silent Electric Discharge.by Mercury-Photosensitized Photolyses.; from Bissilylmercury Compounds; by Thermolysis.; by Photolysis.; from Organosilanes and Silicon Halides by Hydrogenolysis.; from Silylenes; by Oligomerization.; by Insertions into Bonds of Silicon to Hydrogen, Oxygen and Silicon.; by Addition to Si = C.; in the Direct Reaction of Methyl Chloride with Silicon-Copper.; Formation of the Germanium-Germanium Bond; in Elemental Germanium; from Oxides.; from Sulfides.; by Other Syntheses.; Formation of High-Purity Germanium.; from Organogermanium Hydrides
by Reaction with Diorganomercury Compounds in the Presence of UV Radiation.by Hydrogermolysis Reaction.; by Germanium Hydride Decomposition.; from Ge(lV) Halides and Organogermanium(IV) Halides; by the Action of a Microwave Discharge of Ge(lV) Halides.; by Electrochemical Reduction.; by Halide Elimination with Active Metals.; by Reaction with Germyl-Metal Reagents.; by Reaction with Organometallic Reagents.; from Germanium(lI) Halides; by Reactions with Germyl-Metal Reagents.; by Reaction with Organometallic Reagents.; from Germyl Compounds of Cadmium, Mercury, Thallium, Antimony and Bismuth
by Thermolysis or Photolysis.from Germylenes; by Oligomerization of Germylenes.; by Insertions into Bonds of Germanium to Hydrogen, Halogen, Carbon, Oxygen, Sulfur, Nitrogen, Phosphorus and Germanium.; The Formation of the Tin-Tin Bond; in Elemental Tin; from Oxides.; from Sulfides.; by Other Syntheses.; Allotropy of Tin; from Organotin Hydrides; by Catalytic Hydrogen Elimination.; by Reaction with Organotin Halogen, Pseudohalogen, Chalcogen and Pnictogen Compounds.; by Reaction with Organometallic Compounds.; by Reaction with Reducible Organic Compounds.; from Organotin Halides
by Electrochemical Reduction.
Record Nr. UNISA-996211962403316
New York, N.Y., : VCH Publishers, 1991
Materiale a stampa
Lo trovi qui: Univ. di Salerno
Opac: Controlla la disponibilità qui
Formation of bonds to C, Si, Ge, Sn, Pb . Part 1 [[electronic resource] /] / founding editor, J.J. Zuckerman; editor, A.P. Hagen
Formation of bonds to C, Si, Ge, Sn, Pb . Part 1 [[electronic resource] /] / founding editor, J.J. Zuckerman; editor, A.P. Hagen
Pubbl/distr/stampa New York, N.Y., : VCH Publishers, 1991
Descrizione fisica 1 online resource (633 p.)
Disciplina 541.3/9
541.39
Altri autori (Persone) ZuckermanJ. J <1936-1987.> (Jerold J.)
HagenA. P
Collana Inorganic reactions and methods
Soggetto topico Chemical kinetics - Effect of temperature on
Inorganic compounds - Synthesis
ISBN 1-282-30813-0
9786612308130
0-470-14523-4
0-470-14544-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Inorganic Reactions and Methods; Contents; How to use this book; Preface to the Series; Editorial Consultants to the Series; Contributors to Volume 9; Formation of the Bonds to the Group-IVB (C, Si, Ge, Sn, Pb) Elements; Introduction; Formation of the Group-IVB (C, Si, Ge, Sn, Pb)-Group-IVB (C, Si, Ge, Sn, Pb) Element Bond; Introduction; Formation of the Carbon-Carbon Bond; Formation of the Si-Si Bond; in Elemental Silicon; from Oxides.; by Other Methods.; Formation of High-Purity Silicon; Electrochemical Formation of Compounds with Si-Si Bonds (Including Elemental Silicon)
from Metal Silicidesby Solvolysis in Aqueous or Liquid Ammonia Solutions.; Formation of Oligosilanes; Formation of Polymeric Compounds; from Silicon Hydrides and Organosilicon Hydrides; by the Action of a Silent Electric Discharge.; by Direct Photolysis.; by Sensitized Photolysis.; by Catalyzed Reactions.; by Reaction with Silylmetallic Compounds.; from Silicon Halides and Organosilicon Halides; by Electrochemical Reduction.; by Halide Elimination with Active Metals.; by Reaction with Silylmetallics.; by Catalyzed Disproportionation.; by Reaction with Organomagnesium Halide Reagents.
by the Action of Silent Electric Discharge.by Mercury-Photosensitized Photolyses.; from Bissilylmercury Compounds; by Thermolysis.; by Photolysis.; from Organosilanes and Silicon Halides by Hydrogenolysis.; from Silylenes; by Oligomerization.; by Insertions into Bonds of Silicon to Hydrogen, Oxygen and Silicon.; by Addition to Si = C.; in the Direct Reaction of Methyl Chloride with Silicon-Copper.; Formation of the Germanium-Germanium Bond; in Elemental Germanium; from Oxides.; from Sulfides.; by Other Syntheses.; Formation of High-Purity Germanium.; from Organogermanium Hydrides
by Reaction with Diorganomercury Compounds in the Presence of UV Radiation.by Hydrogermolysis Reaction.; by Germanium Hydride Decomposition.; from Ge(lV) Halides and Organogermanium(IV) Halides; by the Action of a Microwave Discharge of Ge(lV) Halides.; by Electrochemical Reduction.; by Halide Elimination with Active Metals.; by Reaction with Germyl-Metal Reagents.; by Reaction with Organometallic Reagents.; from Germanium(lI) Halides; by Reactions with Germyl-Metal Reagents.; by Reaction with Organometallic Reagents.; from Germyl Compounds of Cadmium, Mercury, Thallium, Antimony and Bismuth
by Thermolysis or Photolysis.from Germylenes; by Oligomerization of Germylenes.; by Insertions into Bonds of Germanium to Hydrogen, Halogen, Carbon, Oxygen, Sulfur, Nitrogen, Phosphorus and Germanium.; The Formation of the Tin-Tin Bond; in Elemental Tin; from Oxides.; from Sulfides.; by Other Syntheses.; Allotropy of Tin; from Organotin Hydrides; by Catalytic Hydrogen Elimination.; by Reaction with Organotin Halogen, Pseudohalogen, Chalcogen and Pnictogen Compounds.; by Reaction with Organometallic Compounds.; by Reaction with Reducible Organic Compounds.; from Organotin Halides
by Electrochemical Reduction.
Record Nr. UNINA-9910830155803321
New York, N.Y., : VCH Publishers, 1991
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Formation of bonds to C, Si, Ge, Sn, Pb . Part 1 / / founding editor, J.J. Zuckerman; editor, A.P. Hagen
Formation of bonds to C, Si, Ge, Sn, Pb . Part 1 / / founding editor, J.J. Zuckerman; editor, A.P. Hagen
Pubbl/distr/stampa New York, N.Y., : VCH Publishers, 1991
Descrizione fisica 1 online resource (633 p.)
Disciplina 541.3/9
541.39
Altri autori (Persone) ZuckermanJ. J <1936-1987.> (Jerold J.)
HagenA. P
Collana Inorganic reactions and methods
Soggetto topico Chemical kinetics - Effect of temperature on
Inorganic compounds - Synthesis
ISBN 1-282-30813-0
9786612308130
0-470-14523-4
0-470-14544-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Inorganic Reactions and Methods; Contents; How to use this book; Preface to the Series; Editorial Consultants to the Series; Contributors to Volume 9; Formation of the Bonds to the Group-IVB (C, Si, Ge, Sn, Pb) Elements; Introduction; Formation of the Group-IVB (C, Si, Ge, Sn, Pb)-Group-IVB (C, Si, Ge, Sn, Pb) Element Bond; Introduction; Formation of the Carbon-Carbon Bond; Formation of the Si-Si Bond; in Elemental Silicon; from Oxides.; by Other Methods.; Formation of High-Purity Silicon; Electrochemical Formation of Compounds with Si-Si Bonds (Including Elemental Silicon)
from Metal Silicidesby Solvolysis in Aqueous or Liquid Ammonia Solutions.; Formation of Oligosilanes; Formation of Polymeric Compounds; from Silicon Hydrides and Organosilicon Hydrides; by the Action of a Silent Electric Discharge.; by Direct Photolysis.; by Sensitized Photolysis.; by Catalyzed Reactions.; by Reaction with Silylmetallic Compounds.; from Silicon Halides and Organosilicon Halides; by Electrochemical Reduction.; by Halide Elimination with Active Metals.; by Reaction with Silylmetallics.; by Catalyzed Disproportionation.; by Reaction with Organomagnesium Halide Reagents.
by the Action of Silent Electric Discharge.by Mercury-Photosensitized Photolyses.; from Bissilylmercury Compounds; by Thermolysis.; by Photolysis.; from Organosilanes and Silicon Halides by Hydrogenolysis.; from Silylenes; by Oligomerization.; by Insertions into Bonds of Silicon to Hydrogen, Oxygen and Silicon.; by Addition to Si = C.; in the Direct Reaction of Methyl Chloride with Silicon-Copper.; Formation of the Germanium-Germanium Bond; in Elemental Germanium; from Oxides.; from Sulfides.; by Other Syntheses.; Formation of High-Purity Germanium.; from Organogermanium Hydrides
by Reaction with Diorganomercury Compounds in the Presence of UV Radiation.by Hydrogermolysis Reaction.; by Germanium Hydride Decomposition.; from Ge(lV) Halides and Organogermanium(IV) Halides; by the Action of a Microwave Discharge of Ge(lV) Halides.; by Electrochemical Reduction.; by Halide Elimination with Active Metals.; by Reaction with Germyl-Metal Reagents.; by Reaction with Organometallic Reagents.; from Germanium(lI) Halides; by Reactions with Germyl-Metal Reagents.; by Reaction with Organometallic Reagents.; from Germyl Compounds of Cadmium, Mercury, Thallium, Antimony and Bismuth
by Thermolysis or Photolysis.from Germylenes; by Oligomerization of Germylenes.; by Insertions into Bonds of Germanium to Hydrogen, Halogen, Carbon, Oxygen, Sulfur, Nitrogen, Phosphorus and Germanium.; The Formation of the Tin-Tin Bond; in Elemental Tin; from Oxides.; from Sulfides.; by Other Syntheses.; Allotropy of Tin; from Organotin Hydrides; by Catalytic Hydrogen Elimination.; by Reaction with Organotin Halogen, Pseudohalogen, Chalcogen and Pnictogen Compounds.; by Reaction with Organometallic Compounds.; by Reaction with Reducible Organic Compounds.; from Organotin Halides
by Electrochemical Reduction.
Record Nr. UNINA-9910876729803321
New York, N.Y., : VCH Publishers, 1991
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Formation of bonds to C, Si, Ge, Sn, Pb . Part 2 [[electronic resource] /] / founding editor, J.J. Zuckerman ; editor, A.P. Hagen
Formation of bonds to C, Si, Ge, Sn, Pb . Part 2 [[electronic resource] /] / founding editor, J.J. Zuckerman ; editor, A.P. Hagen
Pubbl/distr/stampa New York, N.Y., : VCH, c1989
Descrizione fisica 1 online resource (541 p.)
Disciplina 541.3/9
541.39
Altri autori (Persone) ZuckermanJ. J <1936-1987.> (Jerold J.)
HagenA. P
Collana Inorganic reactions and methods
Soggetto topico Chemical kinetics - Effect of temperature on
Inorganic compounds - Synthesis
Soggetto genere / forma Electronic books.
ISBN 1-282-30808-4
9786612308086
0-470-14524-2
0-470-14545-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Inorganic Reactions and Methods; Contents; How to Use this Book; Preface to the Series; Editorial Consultants to the Series; Contributors to Volume 10; The Formation of Bonds to the Group-IVB Elements (C, Si, Ge, Sn, Pb) (Part 2); Formation of Bonds between Elements of Group IVB (C, Si, Ge, Sn, Pb) and Group IllB (B, Al, Ga, In, TI); Introduction; Formation of Carbon-Boron Bonds; Industrial Preparation of Boron Carbide.; Industrial Preparation of Boron-Carbide Powders.; Densification of Powders.; Laboratory Preparation of Boron Carbide (from the Elements or Boron Halides)
by Direct Synthesis.by Reduction of BCI3 by H2 in the Presence of Carbon.; by Chemical Vapor Deposition (CVD).; by Reduction of Boric Anhydride at Low Temperatures.; by Plasma Synthesis.; by Physical Vapor Deposition (PVD).; Crystal Growth.; Boron Carbide Fibers.; from Boron Halides; by Reaction with More Polar Organometallics (Metal-Metal Exchange, Excluding Amino-, Oxo- and Thioboron Halides).; by Reaction with an Organoboron-Active-Metal Reagent.; by Substitution of Hydrocarbons.; by Addition to Olefinic and Acetylenic Linkages (Haloboration).; by Reaction with Diazoalkanes.
by Redistribution Reactions with Organoboranes.from Boron Alkoxides with More Polar Organometallics; Alkyl- and Arylboronic Acids.; Alkyl- and Arylborinic Acids.; to form Organoboranes with Three B-C Bonds.; from Boron Hyrides; by Addition to Olefins and Acetylenes (Hydroboration).; by Addition to Polar Organometallics to Form Organoborates.; by Redistribution of Organoboron Hydrides.; from Organoboranes; by Redistribution.; by lsomerization and Displacement.; by Pyrolytic Elimination of H2.; by Addition of Olefinic and Acetylenic Linkages (Carboboration).; from Larger Boranes and Carboranes
by Hydroboration of a Polyborane.by Modified Metal Halide-Catalyzed Alkylations with Organic Halides at a Boron Site.; by B,B Addition of Polyboranes to Alkynes.; by Boron Hydrides with Acetylides, Cyanides, or lsocyanides.; by CO Displacements from Polyboranes.; by Other Reactions Using Polyboranes.; Formation of Carbon-Al Bonds; from the Elements; from Al Metal and Its Alloys; by the Interaction of H2 Olefin and Al Metal.; by the Action of Organic Halides on Al.; by the Reaction of Organomercurials with Al.; from Al Halides or Organoaluminum Halides; by Reaction with Polar Organometallics.
by Redistribution with Organoaluminums.by the Interaction with an Active-Metal Hydride and Olefin.; by the Dehalogenation of RnAIX3- n with Active Metals.; from Al Hydrides or Complex Al Hydrides; by Addition to Olefins or Acetylenes (Hydroalumination).; by Transfer of Al Hydride from One Olefin to Another-Al Alkyl-Olefin Displacement.; by Redistribution with Organoaluminums.; by Exchange with Other Organometallics.; from Other Organoaluminum Compounds; by Addition of R-AI Bonds to Olefins or Acetylenes (Carbalumination).
by Substitution of Acidic Carbon-Hydrogen Bonds by Carbon-Al Bonds (Alumination).
Record Nr. UNINA-9910144322203321
New York, N.Y., : VCH, c1989
Materiale a stampa
Lo trovi qui: Univ. Federico II
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