Aqueous-Phase Organometallic Catalysis: Concepts and Applications, 2nd, Complete
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1
Aqueous-Phase Organometallic Catalysis: Concepts and Applications (2004)
DE HC NWISBN: 9783527307128 bzw. 3527307125, in Deutsch, Wiley-VCH, gebundenes Buch, neu, mit Einband.
Lieferung aus: Vereinigte Staaten von Amerika, Versandkostenfrei.
Von Händler/Antiquariat, Book Deals [60506629], Lewiston, NY, U.S.A.
Brand New, Unread Copy in Perfect Condition. A+ Customer Service! Summary: 1 Introduction.1 Introduction (B. Cornils, W.A. Herrmann).2 Basic Aqueous Chemistry.2.1 Organic Chemistry in Water (A. Lubineau, J. Aug, M.-C. Scherrmann).2.1.1 Introduction.2.1.2 Origin of the Reactivity in Water.2.1.3 Pericyclic Reactions.2.1.3.1 Diels - Alder Reactions.2.1.3.2 Hetero Diels -Alder Reactions.2.1.3.3 Other Cycloadditions.2.1.3.4 Claisen Rearrangements.2.1.4 Carbonyl Additions.2.1.4.1 Aldol-type Reactions.2.1.4.2 Michael-type Reactions.2.1.4.3 Allylation Reactions.2.1.5 Oxido-reductions.2.1.5.1 Oxidations.2.1.5.2 Reductions.2.1.6 Radical Reactions.2.1.7 Outlook.2.2 Organometallic Chemistry in Water (W.A. Herrmann, F.E. Khn).2.2.1 Introduction.2.2.2 Water as a Solvent and Ligand.2.2.3 Organometallic Reactions of Water.2.2.4 Catalytic Reactions with Water.2.2.4.1 Water-gas Shift Reaction.2.2.4.2 Wacker- Hoechst Acetaldehyde Process.2.2.4.3 Olefin Hydration.2.2.4.4 Hydrodimerization.2.2.5 Water-soluble Metal Complexes.2.2.6 Perspectives.2.3 Characterization of Organometallic Compounds in Water (G. Laurenczy).2.3.1 Introduction.2.3.2 General Survey.2.3.3 Effect of High Hydrostatic Pressure on Aqueous Organometallic Systems.2.3.4 Aqueous Organometallics with Pressurized Gases.2.3.5 Concluding Remarks.3 Catalysts for an Aqueous Catalysis.3.1 Variation of Central Atoms.3.1.1 Transition Metals (D.J. Darensbourg, C.G. Ortiz).3.1.1.1 Introduction.3.1.1.2 Water-soluble Catalysts by Virtue of Water-soluble Ligands.3.1.1.3 Water-soluble Catalysts through Water Coordination.3.1.2 Lanthanides in Aqueous-phase Catalysis (S. Kobayashi).3.1.2.1 Introduction.3.1.2.2 Aldol Reactions.3.1.2.3 Mannich-type Reactions.3.1.2.4 Diels - Alder Reactions.3.1.2.5 Micellar Systems.3.1.2.6 Asymmetric Catalysis in Aqueous Media.3.1.2.7 Conclusions.3.2 Variation of Ligands.3.2.1 Monophosphines (O. Stelzer , S. Rossenbach, D. Hoff).3.2.1.1 General Features, Scope, and Limitations.3.2.1.2 Anionic Phosphines.3.2.1.3 Cationic Phosphines.3.2.1.4 Nonionic Water-soluble Phosphines.3.2.2 Diphosphines and Other Phosphines (M. Schreuder Goedheijt, P.C.J. Kamer, J.N.H. Reek, P.W.N.M. van Leeuwen).3.2.2.1 General.3.2.2.2 Diphosphines - Introduction of Sulfonate Groups by Direct Sulfonation.3.2.2.3 Introduction of Sulfonate Groups During Synthesis.3.2.2.4 Diphosphines with Quaternized Aminoalkyl or Aminoaryl Groups.3.2.2.5 Diphosphines with Hydroxyalkyl or Polyether Substituents.3.2.2.6 Carboxylated Diphosphines.3.2.2.7 Amphiphilic Diphosphines.3.2.2.8 Other Phosphines.3.2.3 Ligands or Complexes Containing Ancillary Functionalities (P. Kalck, M. Urrutigoity).3.2.3.1 Complexes Containing at Least Two Classical Functionalities.3.2.3.2 Cationic Complexes.3.2.3.3 Immobilization on Silica Supports.3.2.3.4 Macromolecular Ligands or Supports.3.2.3.5 Ligands not Containing Phosphorus.3.2.3.6 Additional Perspectives.3.2.4 Tenside Ligands (G. Papadogianakis).3.2.4.1 Introduction.3.2.4.2 Tenside Phosphines and Amines.3.2.4.3 Hydroformylation Reactions Catalyzed by Transition Metal Surfactant -Phosphine Complexes.3.2.4.4 Hydrogenation Reactions Catalyzed by Transition Metal Surfactant -Phosphine Complexes.3.2.4.5 Carbonylation Reactions Catalyzed by Transition Metal Surfactant -Phosphine Complexes.3.2.4.6 Concluding Remarks and Future Prospects.3.2.5 Chiral Ligands (W.A. Herrmann, R.W. Eckl, F.E. Khn).3.2.5.1 Introduction.3.2.5.2 Sulfonated Chiral Phosphines.3.2.5.3 Other Water-soluble Chiral Ligands.3.2.5.4 Conclusions.3.2.6 Other Concepts (A. Brner).3.2.6.1 Hydroxyphosphines as Ligands.3.2.6.2 Amines and Polyoxometallates as Ligands (W.A. Herrmann, C.-P. Reisinger).4 Catalysis in Water as a Special Unit Operation.4.1 Fundamentals of Biphasic Reactions in Water (Y.nal, M. Baerns, P. Claus).4.1.1 Introduction.4.1.2 Gas/Liquid-phase Reactions.4.1.3 Gas/Liquid/Liquid-phase Reactions.4.1.4 Place of Reaction in Aqueous Biphasic Systems.4.2 Technical Concepts (A. Behr).4.2.1 Reaction Systems.4.2.2 Tec.
Von Händler/Antiquariat, Book Deals [60506629], Lewiston, NY, U.S.A.
Brand New, Unread Copy in Perfect Condition. A+ Customer Service! Summary: 1 Introduction.1 Introduction (B. Cornils, W.A. Herrmann).2 Basic Aqueous Chemistry.2.1 Organic Chemistry in Water (A. Lubineau, J. Aug, M.-C. Scherrmann).2.1.1 Introduction.2.1.2 Origin of the Reactivity in Water.2.1.3 Pericyclic Reactions.2.1.3.1 Diels - Alder Reactions.2.1.3.2 Hetero Diels -Alder Reactions.2.1.3.3 Other Cycloadditions.2.1.3.4 Claisen Rearrangements.2.1.4 Carbonyl Additions.2.1.4.1 Aldol-type Reactions.2.1.4.2 Michael-type Reactions.2.1.4.3 Allylation Reactions.2.1.5 Oxido-reductions.2.1.5.1 Oxidations.2.1.5.2 Reductions.2.1.6 Radical Reactions.2.1.7 Outlook.2.2 Organometallic Chemistry in Water (W.A. Herrmann, F.E. Khn).2.2.1 Introduction.2.2.2 Water as a Solvent and Ligand.2.2.3 Organometallic Reactions of Water.2.2.4 Catalytic Reactions with Water.2.2.4.1 Water-gas Shift Reaction.2.2.4.2 Wacker- Hoechst Acetaldehyde Process.2.2.4.3 Olefin Hydration.2.2.4.4 Hydrodimerization.2.2.5 Water-soluble Metal Complexes.2.2.6 Perspectives.2.3 Characterization of Organometallic Compounds in Water (G. Laurenczy).2.3.1 Introduction.2.3.2 General Survey.2.3.3 Effect of High Hydrostatic Pressure on Aqueous Organometallic Systems.2.3.4 Aqueous Organometallics with Pressurized Gases.2.3.5 Concluding Remarks.3 Catalysts for an Aqueous Catalysis.3.1 Variation of Central Atoms.3.1.1 Transition Metals (D.J. Darensbourg, C.G. Ortiz).3.1.1.1 Introduction.3.1.1.2 Water-soluble Catalysts by Virtue of Water-soluble Ligands.3.1.1.3 Water-soluble Catalysts through Water Coordination.3.1.2 Lanthanides in Aqueous-phase Catalysis (S. Kobayashi).3.1.2.1 Introduction.3.1.2.2 Aldol Reactions.3.1.2.3 Mannich-type Reactions.3.1.2.4 Diels - Alder Reactions.3.1.2.5 Micellar Systems.3.1.2.6 Asymmetric Catalysis in Aqueous Media.3.1.2.7 Conclusions.3.2 Variation of Ligands.3.2.1 Monophosphines (O. Stelzer , S. Rossenbach, D. Hoff).3.2.1.1 General Features, Scope, and Limitations.3.2.1.2 Anionic Phosphines.3.2.1.3 Cationic Phosphines.3.2.1.4 Nonionic Water-soluble Phosphines.3.2.2 Diphosphines and Other Phosphines (M. Schreuder Goedheijt, P.C.J. Kamer, J.N.H. Reek, P.W.N.M. van Leeuwen).3.2.2.1 General.3.2.2.2 Diphosphines - Introduction of Sulfonate Groups by Direct Sulfonation.3.2.2.3 Introduction of Sulfonate Groups During Synthesis.3.2.2.4 Diphosphines with Quaternized Aminoalkyl or Aminoaryl Groups.3.2.2.5 Diphosphines with Hydroxyalkyl or Polyether Substituents.3.2.2.6 Carboxylated Diphosphines.3.2.2.7 Amphiphilic Diphosphines.3.2.2.8 Other Phosphines.3.2.3 Ligands or Complexes Containing Ancillary Functionalities (P. Kalck, M. Urrutigoity).3.2.3.1 Complexes Containing at Least Two Classical Functionalities.3.2.3.2 Cationic Complexes.3.2.3.3 Immobilization on Silica Supports.3.2.3.4 Macromolecular Ligands or Supports.3.2.3.5 Ligands not Containing Phosphorus.3.2.3.6 Additional Perspectives.3.2.4 Tenside Ligands (G. Papadogianakis).3.2.4.1 Introduction.3.2.4.2 Tenside Phosphines and Amines.3.2.4.3 Hydroformylation Reactions Catalyzed by Transition Metal Surfactant -Phosphine Complexes.3.2.4.4 Hydrogenation Reactions Catalyzed by Transition Metal Surfactant -Phosphine Complexes.3.2.4.5 Carbonylation Reactions Catalyzed by Transition Metal Surfactant -Phosphine Complexes.3.2.4.6 Concluding Remarks and Future Prospects.3.2.5 Chiral Ligands (W.A. Herrmann, R.W. Eckl, F.E. Khn).3.2.5.1 Introduction.3.2.5.2 Sulfonated Chiral Phosphines.3.2.5.3 Other Water-soluble Chiral Ligands.3.2.5.4 Conclusions.3.2.6 Other Concepts (A. Brner).3.2.6.1 Hydroxyphosphines as Ligands.3.2.6.2 Amines and Polyoxometallates as Ligands (W.A. Herrmann, C.-P. Reisinger).4 Catalysis in Water as a Special Unit Operation.4.1 Fundamentals of Biphasic Reactions in Water (Y.nal, M. Baerns, P. Claus).4.1.1 Introduction.4.1.2 Gas/Liquid-phase Reactions.4.1.3 Gas/Liquid/Liquid-phase Reactions.4.1.4 Place of Reaction in Aqueous Biphasic Systems.4.2 Technical Concepts (A. Behr).4.2.1 Reaction Systems.4.2.2 Tec.
2
Aqueous-Phase Organometallic Catalysis: Concepts and Applications (2004)
DE HCISBN: 9783527307128 bzw. 3527307125, in Deutsch, Wiley-VCH, gebundenes Buch, mit Einband.
Lieferung aus: Vereinigte Staaten von Amerika, Versandkostenfrei.
Von Händler/Antiquariat, Book Deals [60506629], Lewiston, NY, U.S.A.
This Book is in Good Condition. Clean Copy With Light Amount of Wear. 100% Guaranteed. Summary: 1 Introduction.1 Introduction (B. Cornils, W.A. Herrmann).2 Basic Aqueous Chemistry.2.1 Organic Chemistry in Water (A. Lubineau, J. Aug, M.-C. Scherrmann).2.1.1 Introduction.2.1.2 Origin of the Reactivity in Water.2.1.3 Pericyclic Reactions.2.1.3.1 Diels - Alder Reactions.2.1.3.2 Hetero Diels -Alder Reactions.2.1.3.3 Other Cycloadditions.2.1.3.4 Claisen Rearrangements.2.1.4 Carbonyl Additions.2.1.4.1 Aldol-type Reactions.2.1.4.2 Michael-type Reactions.2.1.4.3 Allylation Reactions.2.1.5 Oxido-reductions.2.1.5.1 Oxidations.2.1.5.2 Reductions.2.1.6 Radical Reactions.2.1.7 Outlook.2.2 Organometallic Chemistry in Water (W.A. Herrmann, F.E. Khn).2.2.1 Introduction.2.2.2 Water as a Solvent and Ligand.2.2.3 Organometallic Reactions of Water.2.2.4 Catalytic Reactions with Water.2.2.4.1 Water-gas Shift Reaction.2.2.4.2 Wacker- Hoechst Acetaldehyde Process.2.2.4.3 Olefin Hydration.2.2.4.4 Hydrodimerization.2.2.5 Water-soluble Metal Complexes.2.2.6 Perspectives.2.3 Characterization of Organometallic Compounds in Water (G. Laurenczy).2.3.1 Introduction.2.3.2 General Survey.2.3.3 Effect of High Hydrostatic Pressure on Aqueous Organometallic Systems.2.3.4 Aqueous Organometallics with Pressurized Gases.2.3.5 Concluding Remarks.3 Catalysts for an Aqueous Catalysis.3.1 Variation of Central Atoms.3.1.1 Transition Metals (D.J. Darensbourg, C.G. Ortiz).3.1.1.1 Introduction.3.1.1.2 Water-soluble Catalysts by Virtue of Water-soluble Ligands.3.1.1.3 Water-soluble Catalysts through Water Coordination.3.1.2 Lanthanides in Aqueous-phase Catalysis (S. Kobayashi).3.1.2.1 Introduction.3.1.2.2 Aldol Reactions.3.1.2.3 Mannich-type Reactions.3.1.2.4 Diels - Alder Reactions.3.1.2.5 Micellar Systems.3.1.2.6 Asymmetric Catalysis in Aqueous Media.3.1.2.7 Conclusions.3.2 Variation of Ligands.3.2.1 Monophosphines (O. Stelzer , S. Rossenbach, D. Hoff).3.2.1.1 General Features, Scope, and Limitations.3.2.1.2 Anionic Phosphines.3.2.1.3 Cationic Phosphines.3.2.1.4 Nonionic Water-soluble Phosphines.3.2.2 Diphosphines and Other Phosphines (M. Schreuder Goedheijt, P.C.J. Kamer, J.N.H. Reek, P.W.N.M. van Leeuwen).3.2.2.1 General.3.2.2.2 Diphosphines - Introduction of Sulfonate Groups by Direct Sulfonation.3.2.2.3 Introduction of Sulfonate Groups During Synthesis.3.2.2.4 Diphosphines with Quaternized Aminoalkyl or Aminoaryl Groups.3.2.2.5 Diphosphines with Hydroxyalkyl or Polyether Substituents.3.2.2.6 Carboxylated Diphosphines.3.2.2.7 Amphiphilic Diphosphines.3.2.2.8 Other Phosphines.3.2.3 Ligands or Complexes Containing Ancillary Functionalities (P. Kalck, M. Urrutigoity).3.2.3.1 Complexes Containing at Least Two Classical Functionalities.3.2.3.2 Cationic Complexes.3.2.3.3 Immobilization on Silica Supports.3.2.3.4 Macromolecular Ligands or Supports.3.2.3.5 Ligands not Containing Phosphorus.3.2.3.6 Additional Perspectives.3.2.4 Tenside Ligands (G. Papadogianakis).3.2.4.1 Introduction.3.2.4.2 Tenside Phosphines and Amines.3.2.4.3 Hydroformylation Reactions Catalyzed by Transition Metal Surfactant -Phosphine Complexes.3.2.4.4 Hydrogenation Reactions Catalyzed by Transition Metal Surfactant -Phosphine Complexes.3.2.4.5 Carbonylation Reactions Catalyzed by Transition Metal Surfactant -Phosphine Complexes.3.2.4.6 Concluding Remarks and Future Prospects.3.2.5 Chiral Ligands (W.A. Herrmann, R.W. Eckl, F.E. Khn).3.2.5.1 Introduction.3.2.5.2 Sulfonated Chiral Phosphines.3.2.5.3 Other Water-soluble Chiral Ligands.3.2.5.4 Conclusions.3.2.6 Other Concepts (A. Brner).3.2.6.1 Hydroxyphosphines as Ligands.3.2.6.2 Amines and Polyoxometallates as Ligands (W.A. Herrmann, C.-P. Reisinger).4 Catalysis in Water as a Special Unit Operation.4.1 Fundamentals of Biphasic Reactions in Water (Y.nal, M. Baerns, P. Claus).4.1.1 Introduction.4.1.2 Gas/Liquid-phase Reactions.4.1.3 Gas/Liquid/Liquid-phase Reactions.4.1.4 Place of Reaction in Aqueous Biphasic Systems.4.2 Technical Concepts (A. Behr).4.2.1 React.
Von Händler/Antiquariat, Book Deals [60506629], Lewiston, NY, U.S.A.
This Book is in Good Condition. Clean Copy With Light Amount of Wear. 100% Guaranteed. Summary: 1 Introduction.1 Introduction (B. Cornils, W.A. Herrmann).2 Basic Aqueous Chemistry.2.1 Organic Chemistry in Water (A. Lubineau, J. Aug, M.-C. Scherrmann).2.1.1 Introduction.2.1.2 Origin of the Reactivity in Water.2.1.3 Pericyclic Reactions.2.1.3.1 Diels - Alder Reactions.2.1.3.2 Hetero Diels -Alder Reactions.2.1.3.3 Other Cycloadditions.2.1.3.4 Claisen Rearrangements.2.1.4 Carbonyl Additions.2.1.4.1 Aldol-type Reactions.2.1.4.2 Michael-type Reactions.2.1.4.3 Allylation Reactions.2.1.5 Oxido-reductions.2.1.5.1 Oxidations.2.1.5.2 Reductions.2.1.6 Radical Reactions.2.1.7 Outlook.2.2 Organometallic Chemistry in Water (W.A. Herrmann, F.E. Khn).2.2.1 Introduction.2.2.2 Water as a Solvent and Ligand.2.2.3 Organometallic Reactions of Water.2.2.4 Catalytic Reactions with Water.2.2.4.1 Water-gas Shift Reaction.2.2.4.2 Wacker- Hoechst Acetaldehyde Process.2.2.4.3 Olefin Hydration.2.2.4.4 Hydrodimerization.2.2.5 Water-soluble Metal Complexes.2.2.6 Perspectives.2.3 Characterization of Organometallic Compounds in Water (G. Laurenczy).2.3.1 Introduction.2.3.2 General Survey.2.3.3 Effect of High Hydrostatic Pressure on Aqueous Organometallic Systems.2.3.4 Aqueous Organometallics with Pressurized Gases.2.3.5 Concluding Remarks.3 Catalysts for an Aqueous Catalysis.3.1 Variation of Central Atoms.3.1.1 Transition Metals (D.J. Darensbourg, C.G. Ortiz).3.1.1.1 Introduction.3.1.1.2 Water-soluble Catalysts by Virtue of Water-soluble Ligands.3.1.1.3 Water-soluble Catalysts through Water Coordination.3.1.2 Lanthanides in Aqueous-phase Catalysis (S. Kobayashi).3.1.2.1 Introduction.3.1.2.2 Aldol Reactions.3.1.2.3 Mannich-type Reactions.3.1.2.4 Diels - Alder Reactions.3.1.2.5 Micellar Systems.3.1.2.6 Asymmetric Catalysis in Aqueous Media.3.1.2.7 Conclusions.3.2 Variation of Ligands.3.2.1 Monophosphines (O. Stelzer , S. Rossenbach, D. Hoff).3.2.1.1 General Features, Scope, and Limitations.3.2.1.2 Anionic Phosphines.3.2.1.3 Cationic Phosphines.3.2.1.4 Nonionic Water-soluble Phosphines.3.2.2 Diphosphines and Other Phosphines (M. Schreuder Goedheijt, P.C.J. Kamer, J.N.H. Reek, P.W.N.M. van Leeuwen).3.2.2.1 General.3.2.2.2 Diphosphines - Introduction of Sulfonate Groups by Direct Sulfonation.3.2.2.3 Introduction of Sulfonate Groups During Synthesis.3.2.2.4 Diphosphines with Quaternized Aminoalkyl or Aminoaryl Groups.3.2.2.5 Diphosphines with Hydroxyalkyl or Polyether Substituents.3.2.2.6 Carboxylated Diphosphines.3.2.2.7 Amphiphilic Diphosphines.3.2.2.8 Other Phosphines.3.2.3 Ligands or Complexes Containing Ancillary Functionalities (P. Kalck, M. Urrutigoity).3.2.3.1 Complexes Containing at Least Two Classical Functionalities.3.2.3.2 Cationic Complexes.3.2.3.3 Immobilization on Silica Supports.3.2.3.4 Macromolecular Ligands or Supports.3.2.3.5 Ligands not Containing Phosphorus.3.2.3.6 Additional Perspectives.3.2.4 Tenside Ligands (G. Papadogianakis).3.2.4.1 Introduction.3.2.4.2 Tenside Phosphines and Amines.3.2.4.3 Hydroformylation Reactions Catalyzed by Transition Metal Surfactant -Phosphine Complexes.3.2.4.4 Hydrogenation Reactions Catalyzed by Transition Metal Surfactant -Phosphine Complexes.3.2.4.5 Carbonylation Reactions Catalyzed by Transition Metal Surfactant -Phosphine Complexes.3.2.4.6 Concluding Remarks and Future Prospects.3.2.5 Chiral Ligands (W.A. Herrmann, R.W. Eckl, F.E. Khn).3.2.5.1 Introduction.3.2.5.2 Sulfonated Chiral Phosphines.3.2.5.3 Other Water-soluble Chiral Ligands.3.2.5.4 Conclusions.3.2.6 Other Concepts (A. Brner).3.2.6.1 Hydroxyphosphines as Ligands.3.2.6.2 Amines and Polyoxometallates as Ligands (W.A. Herrmann, C.-P. Reisinger).4 Catalysis in Water as a Special Unit Operation.4.1 Fundamentals of Biphasic Reactions in Water (Y.nal, M. Baerns, P. Claus).4.1.1 Introduction.4.1.2 Gas/Liquid-phase Reactions.4.1.3 Gas/Liquid/Liquid-phase Reactions.4.1.4 Place of Reaction in Aqueous Biphasic Systems.4.2 Technical Concepts (A. Behr).4.2.1 React.
3
Aqueous-Phase Organometallic Catalysis
DE NWISBN: 9783527307128 bzw. 3527307125, in Deutsch, John Wiley & Sons, neu.
Von Händler/Antiquariat, Majestic Books [51749587], London, ,, United Kingdom.
Die Beschreibung dieses Angebotes ist von geringer Qualität oder in einer Fremdsprache. Trotzdem anzeigen
Die Beschreibung dieses Angebotes ist von geringer Qualität oder in einer Fremdsprache. Trotzdem anzeigen
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