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Mechanical Catalysis
Methods of Enzymatic, Homogeneous, and Heterogeneous Catalysis
Gerhard Swiegers (Author)
9780470262023, Wiley
Hardback, published 17 October 2008
384 pages
24.3 x 16.3 x 2.3 cm, 0.658 kg
?This book is a useful addition to the library of any individual working with functionalized catalysts, especially those that may undergo conformational changes during the reaction process. This text is especially informative for those working with enzymes, biomimetic, and organometallic-based catalysts. It also unifies many of the kinetic models that have been put forth to describe heterogeneous, homogeneous, and enzymatic catalysis.? (Journal of the American Chemical Society, October 2009)
Preface xxi Contributors xxv Glossary xxvii 1 Introduction to Thermodynamic (Energy-Dependent) and Mechanical (Time-Dependent) Processes: What Are They and How Are They Manifested in Chemistry and Catalysis? 1.1 Thermodynamic (Energy-Dependent) and Mechanical (Time-Dependent) Processes 1 1.2 What Is a Thermodynamic Process? 5 1.3 What Is a Mechanical Process? 7 1.4 The Difference between Energy-Dependent (Thermodynamic) and Time-Dependent (Mechanical) Processes 9 1.4.1 Time-Dependent (Mechanical) Processes Are Path-Reliant and Spatiotemporal in Character 9 1.4.2 Time-Dependent (Mechanical) Processes Have a Flat Underlying Energy Landscape (or Are Unaffected by the Energy Landscape) 10 1.4.3 Time-Dependent (Mechanical) Processes Display Deterministic Chaos; This Causes Them to be Stochastic and Complex 11 1.4.4 Time-Dependent (Mechanical) Processes Often Involve Synergies of Action 14 1.4.5 Time-Dependent (Mechanical) Processes Characterize Numerous Aspects of Human Experience 15 1.5 Time- and Energy-Dependence in Chemistry and Catalysis 17 1.5.1 The Origin of Time- and Energy-Dependent Processes in Chemistry 17 1.5.2 Examples of Time-Dependent Processes in Chemistry 19 1.5.3 Time- and Energy-Dependent Processes in Catalysis 21 1.5.4 Is There Such a Thing as a Time-Dependent Process in Catalysis? 23 1.6 The Aims, Structure, and Major Findings of this Series 24 1.6.1 Summary of the Key Finding: Many Enzymes Seem to be Time-Dependent Catalysts 25 1.6.2 The Aims and Structure of this Series. Summary: Other Major Findings of this Series 28 References 34 2 Heterogeneous, Homogeneous, and Enzymatic Catalysis. A Shared Terminology and Conceptual Platform. The Alternative of Time-Dependence in Catalysis 37 2.1 Introduction: The Problem of Conceptually Unifying Heterogeneous, Homogeneous, and Enzymatic Catalysis? Trends in Catalysis Science 37 2.2 Background: What Is Heterogeneous, Homogeneous, and Enzymatic Catalysis 38 2.2.1 Homogeneous and Heterogeneous Catalysis 38 2.2.2 Hybrid Homogeneous–Heterogeneous Catalysts 40 2.2.3 Enzymatic Catalysis 41 2.2.4 Theories and Mimicry of Enzymatic Catalysis 42 2.3 Distinctions Within Homogeneous Catalysis: Single-Centered and Multicentered Homogeneous Catalysis 44 2.3.1 Single-Centered Homogeneous Catalysts. Most Manmade Homogeneous Catalysts Are Single-Centered Catalysts 44 2.3.2 Multicentered Homogeneous Catalysts: Most Enzymes Are Multicentered Homogeneous Catalysts 46 2.4 The Distinction between Single-Site/Multisite Catalysts and Single-Centered/MultiCentered Catalysts in Heterogeneous Catalysis: An Important Convention Used in This Series 48 2.4.1 A Key Convention Used in This Series: A Catalytic Site Is a Collection of Atoms about Which a Reaction Is Catalyzed. A Catalytic Center Is an Atom Within that Site Which Binds and Facilitates the Transformation of a Reactant 48 2.5 The Alternative of Time-Dependence in Catalysis 48 References 52 3 A Conceptual Description of Energy-Dependent (“Thermodynamic”) and Time-Dependent (“Mechanical”) Processes in Chemistry and Catalysis 55 3.1 Introduction 55 3.2 Theoretical Considerations: Common Processes in Uncatalyzed Reactions 56 3.2.1 Reactions as Collisions Between Molecules 56 3.2.2 The Fundamental Origin of Energy-Dependent and Time-Dependent Reactions 57 3.2.3 Time-Dependent and Energy-Dependent Domains Were First Observed in Unimolecular Gas-Phase Reactions 58 3.2.4 The Pathway of the Reaction Is also Controlled by the Least-Likely Step in the Sequence 59 3.2.5 Transition State Theory (TST) Describes the Pathway and Rate of Energy-Dependent Reactions. Transition State Theory Corresponds to the High-Pressure Limit of Hinshelwood–RRK Theory 61 3.2.6 Time-Dependent Reactions in the Liquid Phase: Some Examples 63 3.2.7 The Transition between Energy-Dependence and Time-Dependence as a Function of Temperature. Curvature in Arrhenius Plots 65 3.2.8 Methods of Creating Time-Dependent Reactions 67 3.2.9 Summary: The Key Properties of Time-Dependent and Energy-Dependent Reactions 68 3.3 Theoretical Considerations: Common Processes in Catalyzed Reactions 68 3.3.1 Catalyzed Reactions Are More Likely to be Time-Dependent than Are Uncatalyzed Reactions 68 3.3.2 Catalysis Changes the Reaction Processes 69 3.3.3 Physical Manifestation of Time- and Energy-Dependence in Catalysts 72 3.3.4 The Distinction Between Time-Dependent Catalysis and Diffusion-Controlled Catalysis 72 3.3.5 Energy-Dependent and Time-Dependent Control of Catalysis 73 3.3.6 The Influence of the Product Release Step 74 3.4 Conclusions: Energy- and Time-Dependent Catalysis 75 Acknowledgments 75 References 76 4 Time-Dependence in Heterogeneous Catalysis. Sabatier’s Principle Describes Two Independent Catalytic Realms: Time-Dependent (“Mechanical”) Catalysis and Energy-Dependent (“Thermodynamic”) Catalysis 77 4.1 Introduction 77 4.2 Sabatier’s Principle in Heterogeneous Catalysis 79 4.2.1 Volcano Plots 79 4.2.2 Some Important Points about Volcano Plots 82 4.2.3 Time-Dependent Catalysis in Volcano Plots 82 4.2.3.1 How Is Time-Dependence Created on the Left-Hand Side of the Volcano Plot? 82 4.2.3.2 Why Do Volcano Plots Slope Upward on the Left 84 4.2.3.3 The Rate-Determining Step in a Time-Dependent Catalyst 86 4.2.3.4 The Physical Manifestation of Time-Dependent Catalysis. “Saturation” of a Time-Dependent Catalyst 87 4.2.4 Energy-Dependent Catalysis in Volcano Plots 88 4.2.4.1 How Is Energy-Dependence Created on the Right-Hand Side of the Volcano Plot? 88 4.2.4.2 Why Do Volcano Plots Slope Downward on the Right? 88 4.2.4.3 The Rate-Determining Step in an Energy-Dependent Catalyst 89 4.2.4.4 The Physical Manifestation of Energy- Dependence. Saturation in an Energy-Dependent Catalyst 89 4.2.5 The Physical Origin of Sabatier’s Principle 89 4.2.6 Other Plots Illustrating Sabatier’s Principle 90 4.2.7 Modeling of Volcano Plots 91 4.2.8 Reaction Pathway as a Function of the Most-Favored Transition State 92 4.3 Exceptions to Sabatier’s Principle 93 4.4 Sabatier’s Principle in Homogeneous Catalysis 93 4.5 Conclusions. Sabatier’s Principle Describes Two Independent Catalytic Domains: Energy- and Time-Dependent Catalysis 94 Acknowledgments 95 References 95 5 Time-Dependence in Homogeneous Catalysis. 1. Many Enzymes Display the Hallmarks of Time-Dependent (“Mechanical”) Catalysis. Nonbiological Homogeneous Catalysts Are Typically Energy-Dependent (“Thermodynamic”) Catalysts 97 5.1 Introduction 97 5.2 Historical Background: Are Enzymes Generally Energy-Dependent or Time-Dependent Catalysts? 99 5.3 The Methodology of This Chapter: Identify, Contrast, and Rationalize the Common Processes Present in Biological and Nonbiological Homogeneous Catalysts 100 5.4 Does Michaelis–Menten Kinetics in Enzymes Indicate that They Are Time-Dependent Catalysts? 102 5.4.1 Michaelis–Menten Kinetics 102 5.4.2 Kinetics in Most Nonbiological Catalysts 103 5.4.3 The Contradiction of Saturation Kinetics in Enzymes 103 5.4.4 Saturation in Time- and Energy-Dependent Catalysts. Saturation Kinetics Is Necessarily an Indication of Time-Dependence 104 5.4.5 Physical Studies of the Rate Processes in Enzymes Are Consistent with a Time-Dependent Action 106 5.4.6 A Time-Dependent Catalyst Cannot Become an Energy-Dependent Catalyst, or vice versa, Without Changing the Temperature or Chemically Altering the Reactivity of the Reactants 107 5.4.7 The Current View of Michaelis–Menten Kinetics Is Flawed by an Unwarranted Assumption 107 5.4.8 Summary: Michaelis–Menten Kinetics Is Characteristic of Time-Dependent Catalysis. Time-Dependent Catalysis Provides an Explanation for Michaelis–Menten Kinetics in Enzymes 109 5.5 Other General Characteristics of Catalysis by Enzymes and Comparable Nonbiological Homogeneous Catalysts 110 5.5.1 Enzymes Employ Weak and Dynamic Individual Binding Interactions with Their Substrates. Nonbiological Catalysts Do Not 110 5.5.2 Enzymes Display Transition State Complementarity. Nonbiological Catalysts Do Not 111 5.5.3 Enzymatic Catalysis Is “Structure-Sensitive.” Nonbiological Catalysis Is “Structure-Insensitive” 112 5.5.4 Enzymes Transform Catalytically Unconventional Groups into Potent Catalysts. Nonbiological Catalysts Use Only Conventional Catalytic Groups 113 5.5.5 Enzymes Catalyze Forward and Reverse Reactions. Nonbiological Catalysts Do Not 113 5.5.6 Enzymes Display High Selectivity and Activity. Nonbiological Catalysts Do Not 115 5.5.7 Enzymes Display Convergent Synergies. Nonbiological Catalysts Display Complementary Synergies 115 5.5.8 Summary 116 5.6 Rationalization of the Underlying Processes. The Mechanism of Action in Time-Dependent and Energy-Dependent Catalysts 117 5.6.1 Common Processes in Multicentered Homogeneous Catalysts 117 5.6.2 The Influence of the Strength of the Individual Catalyst–Reactant Binding Interactions 119 5.6.3 The Coexistence of Transition State Complementarity, Structure-Sensitive Catalysis, and Unconventional Catalytic Groups in Enzymes Is Caused by their Weak Individual Binding Interactions 122 5.6.4 The Origin of the Time-Dependence and the Synergies of Enzymes 123 5.6.5 The Mechanism of Time-Dependence in Enzymes Resolves the Contradiction of a Kinetically Observed Rapidly Forming and Dissociating Intermediate in the Face of Strong Overall Substrate Binding 125 5.6.6 Catalysis in Enzymes Involves Synchronization of Enzyme Binding and Enzyme Flexing 125 5.6.7 Summary: The Origin of the General Properties of Enzymes 127 5.6.8 Catalysis in Nonbiological Analogues Depends on the Activation Energy E a 127 5.6.9 Enzymatic Selectivity and Synergies Derive from Time-Dependence 128 5.6.10 Enzymatic Activity Is Consistent with Time-Dependence 129 5.7 All Generalizations Support Time-Dependence in Enzymes 129 5.8 Time-Dependence in a Nonbiological Catalyst Generates the Distinctive Properties of Enzymes 130 5.9 Conclusion: Many Enzymes Are Time-Dependent Catalysts 133 Acknowledgments 134 References 134 6 Time-Dependence in Homogeneous Catalysis. 2. The General Actions of Time-Dependent (“Mechanical”) and Energy-Dependent (“Thermodynamic”) Catalysts 137 6.1 Introduction 137 6.2 Time- and Energy-Dependent, Multicentered Homogeneous Catalysts 139 6.3 The Action of Energy-Dependent, Multicentered Homogeneous Catalysts 141 6.4 The Action of Time-Dependent, Multicentered Homogeneous Catalysts 146 6.4.1 The Activation Energy E a Does Not Provide a True Measure of the Threshold Energy in Time-Dependent Catalysts 148 6.4.2 Weak and Dynamic Binding and Activation Is Sufficient to Fulfill the Threshold Energy in Time-Dependent Catalysts 149 6.4.3 Transition State Formation in a Time-Dependent Catalyst Can Be Thought of as a Coordinated Mechanical Process 150 6.4.4 Time-Dependent Catalysts Are Machine-Like (Mechanical) in Their Catalytic Action 150 6.4.5 The Origin of Michaelis–Menten Kinetics in Time-Dependent Catalysts 151 6.4.6 Time-Dependent Catalysts like Many Enzymes Display All of the Characteristic Hallmarks of Mechanical Processes 153 6.4.7 Additional Insights into Enzymatic Catalysis: The Bidirectionality of Enzymatic Catalysis Originates from the Mechanical Nature of the Catalytic Action 154 6.4.8 Additional Insights into Enzymatic Catalysis: Many Enzymes Select the First-Encountered Transition State, Rather than the Lowest Energy Transition State 155 6.5 The Importance of Recognizing Time-Dependent Catalysis 155 6.6 Time-Dependent Catalysis Is Very Different to Energy-Dependent Catalysis and Therefore Seems Unfamiliar 156 6.7 Conclusions for Biology 157 6.8 Conclusions for Homogeneous Catalysis 157 6.9 The “Ideal” Homogeneous Catalyst 158 6.10 Conclusions for the Conceptual Unity of the Field of Catalysis 158 Acknowledgments 159 References 159 7 Unifying the Many Theories of Enzymatic Catalysis. Theories of Enzymatic Catalysis Fall into Two Camps: Energy-Dependent (“Thermodynamic”) and Time-Dependent (“Mechanical”) Catalysis 161 7.1 Introduction 161 7.2 Theories of Enzymatic Catalysis 163 7.2.1 Adsorption Theory 163 7.2.2 “Lock-and-Key” Theory 163 7.2.3 Haldane’s Strain Theory 164 7.2.4 Pauling’s Theory of Transition State Complementarity 165 7.2.5 Koshland’s Induced Fit Theory. Fersht’s Concept of Stress and Strain 165 7.2.6 Intramolecularity 165 7.2.7 Orbital Steering 167 7.2.8 Entropy Traps 168 7.2.9 The Proximity (Propinquity) Effect 168 7.2.10 “Coupled” Protein Motions 168 7.2.11 The Spatiotemporal Hypothesis 169 7.3 Theories Explaining Enzymatic Catalysis Fall into Two Camps: Energy-Dependent and Time-Dependent Catalysis 169 7.3.1 Haldane’s Strain Theory and Fersht’s Concept of Stress and Strain Are Valid Explanations for Rate Accelerations but Do Not Seem to be Responsible for the Rate Accelerations of Many Enzymes 171 7.3.2 Theories Based on Reaction Entropy Are Valid Explanations for Rate Accelerations but Do Not Seem to be Behind the Rate Accelerations of Many Enzymes 172 7.3.3 Experiments Studying Intramolecular Reaction Rates Were Probably Often Conceptually Contradictory 172 7.3.4 Theories of “Coupled” Protein Motions and Machine-Like Catalytic Actions Seem to Be Generally Accurate Descriptions of Enzymatic Catalysis 173 7.4 Studies Verifying Pauling’s Theory in Model Systems Are Correct, but Describe Energy-Dependent and not Time-Dependent Catalysis 174 7.5 The Anomaly Described in the Spatiotemporal Hypothesis Originates, in Part, from the Onset of Time-Dependence 176 Acknowledgments 177 !References 177 8 Synergy in Heterogeneous, Homogeneous, and Enzymatic Catalysis. The “Ideal” Catalyst 181 8.1 Introduction 181 8.2 Synergy in Heterogeneous Catalysts 183 8.3 Single-Centered Nonbiological Homogeneous Catalysts and Their ‘Mutually Enhancing’ Synergies 184 8.3.1 Facial Selectivity in Single-Centered Catalysts 184 8.3.2 Energy-Dependent, Single-Centered Homogeneous Catalysts Display ‘Mutually Enhancing’ Synergies 187 8.3.3 The Synergies in Time-Dependent, Single-Centered Homogeneous Catalysts 188 8.3.4 The Selectivity of Single-Centered Catalysts 189 8.4 Multicentered, Energy-Dependent Homogeneous Catalysts and Their Functionally Complementary Synergies 190 8.5 Enzymes and Their Functionally Convergent Synergies 194 8.6 Biomimetic Chemistry and Its Pseudo-Convergent Synergies 197 8.6.1 Cyclodextrin-Appended Epoxidation Catalysts: Pseudo-Convergence in a Nonbiological, Multicentered Catalyst 198 8.7 The Spectrum of Synergistic Action in Homogeneous Catalysis 200 8.7.1 The Relationship Between Complementary and Convergent Synergies 202 8.7.2 The Ideal Catalyst 203 8.8 Synergy in Catalysis Is Conceptually Related to Other Synergistic Processes in Human Experience 205 References 206 9 A Conceptual Unification of Heterogeneous, Homogeneous, and Enzymatic Catalysis 209 9.1 Introduction 209 9.2 Diffusion-Controlled and Reaction-Controlled Catalysis 210 9.3 The Diversity of Catalytic Action in Heterogeneous Catalysts 211 9.4 The Diversity of Catalytic Action in Nonbiological Homogeneous Catalysts 212 9.5 The Diversity of Catalytic Action in Enzymes 214 9.6 Heterogeneous Catalysis and Enzymatic Catalysis Has, Effectively, Involved Combinatorial Experiments that Have Produced Time-Dependent Catalysts. Nonbiological Homogeneous Catalysis Has Not 214 9.7 Homogeneous and Enzymatic Catalysts Are the 3-D Equivalent of 2-D Heterogeneous Catalysts 215 9.8 A Conceptual Unification of Heterogeneous, Homogeneous, and Enzymatic Catalysis 216 References 218 10 The Rational Design of Time-Dependent (“Mechanical”) Homogeneous Catalysts. A Literature Survey of Multicentered Homogeneous Catalysis 219 10.1 Introduction 219 10.2 The Rational Design of Time-Dependent Homogeneous Catalysts 221 10.2.1 Design Criteria for a Time-Dependent Homogeneous Catalyst 221 10.2.2 The Problem of Simultaneously Identifying Suitable Catalytic Groups and Their Active Spatial Arrangement 223 10.2.3 Time-Dependent Homogeneous Catalysis May Conceivably Be Achieved by Mimicry of a Natural Time-Dependent Catalyst 225 10.2.4 Time-Dependent Homogeneous Catalysis May Conceivably Be Achieved in the form of a Combinatorial Experiment Involving a “Statistical Proximity” Effect 226 10.2.4.1 A Time-Dependent Combinatorial Catalyst May Display Unique Kinetics 228 10.2.4.2 Previous Attempts at Concentration-Based Biomimetic Catalysis Involved Energy-Dependent Systems 229 10.2.5 Time-Dependent Catalysis May Be Useful in Transformations of Small Gaseous Molecules 230 10.2.6 Why Do We Need New Time-Dependent Catalysts? 230 10.3 Elements of Rational Design in Multicentered Catalysis 230 10.3.1 Modes of Binding in Multicentered Catalysts 230 10.3.2 Optimizing the Spatial Arrangement of Catalytic Groups 231 10.3.2.1 Intramolecular Catalysts 231 10.3.2.2 Intermolecular Catalysts 233 10.3.2.3 Unconventional Approaches to Optimizing the Spatial Organization of Catalytic Groups 233 10.3.3 Creating Functionally Convergent Catalysts 234 10.3.3.1 Practical Approaches to Achieving Functionally Convergent Catalysis 234 10.4 A Review of Nonbiological, Multicentered Molecular Catalysts Described in the Chemical Literature 235 10.4.1 Intramolecular Catalysts 235 10.4.1.1 Functionally Convergent Catalysis (Class A Type): Cofacial and Capped Metalloporphyrins as Oxygen Reduction Catalysts 235 10.4.1.2 Functionally Convergent Catalysis (Class B Type): [1.1]Ferrocenophanes and Related Compounds as Hydrogen Generation Catalysts 241 10.4.1.3 Pseudoconvergent Catalysis: Supramolecular, Bifunctional Catalysts of Organic Reactions 245 10.4.1.4 Probable Functionally Convergent Catalysis: Rhodium-Phosphine Hydroformylation Catalysts 248 10.4.1.5 Possible Functionally Convergent Catalysis: Ruthenium-Based Water Oxidation Catalysts 249 10.4.1.6 Functionally Complementary Catalysis: Intramolecular Epoxidation Catalysts 252 10.4.1.7 Metal Clusters in Multicentered Molecular Catalysis: Triruthenium Dodecacarbonyl Hydrogenation Catalysts 252 10.4.1.8 Statistical Approaches to Functionally Convergent Catalysis: Macromolecular Intramolecular Catalysts 254 10.4.2 Intermolecular Catalysts 259 10.4.2.1 Functionally Complementary Catalysis 259 10.4.2.2 Statistical Approaches to Functionally Convergent Catalysis: Concentration Effects in Intermolecular Catalysts 260 10.4.2.3 Statistical Approaches to Functionally Convergent Catalysis: Self-Assembled, Supramolecular Catalysts 261 10.4.3 Footnote: Unexpected Mechanistic Changes in Multicentered Catalysts 262 Acknowledgments 263 References 263 11 Time-Dependent (“Mechanical”), Nonbiological Catalysis. 1. A Fully Functional Mimic of the Water-Oxidizing Center (WOC) in Photosystem II (PSII) 267 11.1 Introduction 267 11.2 The Physical and Chemical Properties of the Cubanes 1a-b 273 11.2.1 Chemical Structures 273 11.2.2 Stepwise Hydride Abstraction, Leading to Water Release 275 11.2.3 Dioxygen Generation 275 11.2.4 A Possible Catalytic Cycle 277 11.2.5 Other Reactions 277 11.2.6 Summary 278 11.3 Nafion Provides a Means of Solubilizing and Immobilizing Hydrophobic Metal Complexes 278 11.4 Photoelectrochemical Cells and Dye-Sensitized Solar Cells for Water-Splitting 279 11.5 Photocatalytic Water Oxidation by Cubane 1b Doped into a Nafion Support 282 11.5.1 Solution Electrochemistry 282 11.5.2 Electrochemistry of 1b Doped into a Nafion Membrane 283 11.5.3 Electrocatalytic Effects Are Observed Under cv Conditions 283 11.5.4 a Photo-electrocatalytic Effect Is Observed at 1.00 v (vs. Ag/AgCl) 284 11.5.5 if the Photocurrent Is Caused by Water Oxidation Catalysis, This Involves a Decrease in the Overpotential of 0.4 V 285 11.5.6 The Photocurrent Is Observed only in the Presence of Water. The System Saturates at Low Water Content, Consistent with a Time-Dependent Catalytic Action 286 11.5.7 The pH Dependence of the Photocurrent Is Consistent with Water Oxidation 287 11.5.8 Bulk Water Is a Reactant and Oxygen Is Generated 287 11.5.9 The Quantity of Gas Generated Matches the Current Obtained. Notable Turnover Frequencies Are Implied 287 11.5.10 Photocurrent as a Function of the Illumination Wavelength 290 11.5.11 The Photoaction Spectrum of the Catalysis Corresponds to the Main LMCT Absorption Peak of 1b 290 11.6 The Challenge of Dye-Sensitized Water-Splitting 291 11.7 The Mechanism of the Catalysis 292 11.8 Conclusions 293 References 294 12 Time-Dependent (“Mechanical”), Nonbiological Catalysis. 2. Highly Efficient, “Biomimetic” Hydrogen-Generating Electrocatalysts 297 12.1 Introduction 297 12.2 Monomer and Polymer Preparation 301 12.3 Catalytic Experiments 302 12.3.1 PPy-9 and PPy-12 Display Anodic Shifts in the Most Positive Potential for Hydrogen Generation 302 12.3.2 PPy-9 and PPy-12 Increase the Rate of Hydrogen Generation on Pt by ca. 7-Fold after 12 Hat20.44 V 304 12.3.3 PPy-9 and PPy-12 Increase the Rate of Hydrogen Generation on Pt per Unit Area by ca. 3.5-Fold 307 12.3.4 The Mechanism of Catalysis in PPy-9. Is PPy-9 a Combinatorial (“Statistical Proximity”) Catalyst? 308 12.3.5 Polypyrrole Is Likely Involved in the Catalytic Cycle 309 12.3.6 Other Evidence for the Involvement of Polypyrrole in the Catalytic Cycle 311 12.3.7 The Pyrrole in Polypyrrole Is a Powerful, Time-Dependent, Combinatorial, “Statistical Proximity” Catalyst 313 12.4 Conclusions: A Combinatorial “Statistical Proximity” Catalyst Was Obtained as a Bulk, Hybrid Homogeneous–Heterogeneous Catalyst 316 Acknowledgments 317 References 317 13 Time-Dependent (“Mechanical”), Nonbiological Catalysis. 3. A Readily Prepared, Convergent, Oxygen-Reduction Electrocatalyst 319 13.1 Introduction 319 13.2 Cofacial Diporphyrin Oxygen-Reduction Catalysts 321 13.3 Vapor-Phase Polymerization of Pyrrole as a Means of Immobilizing High Concentrations of Monomeric Catalytic Groups at an Electrode Surface 323 13.4 Preparation and Catalytic Properties of PPy- 3 324 13.4.1 Vapor-Phase Preparation of Polypyrrolle-Co Tetraphenylporphyrin, PPy- 3 324 13.4.2 Electrochemistry of, and Oxygen Reduction by, Polypyrrolle-Co Tetraphenylporphyrin, PPy- 3 324 13.4.3 Rotating Disk Electrochemistry (RDE) of Polypyrrolle-Co Tetraphenylporphyrin, PPy- 3 326 13.4.4 Rotating Ring Disk Electrochemistry (RRDE) of Polypyrrolle-Co Tetraphenylporphyrin, PPy- 3 328 13.4.5 The Product Distribution Relative to the Proportion of 3 in the Polypyrrolle-Co Tetraphenylporphyrin, PPy- 3 329 13.5 PPy-3 as a Fuel Cell Catalyst 330 13.5.1 PPy-3 on Carbon Fiber Paper 330 13.5.2 Electrochemical Characterization of PPy-3 on Carbon Fiber Paper 330 13.5.3 Morphology of the PPy-3 Carbon Fiber Composite Film 330 13.5.4 Oxygen-Reduction Catalysis by the PPy- 3 Carbon Fiber Composite Film in Simple Fuel Cell Test Apparatus 331 13.6 Conclusions 334 References 335 Appendix A Why Is Saturation Not Observed in Catalysts that Display Conventional Kinetics? 337 Appendix B Graphical Illustration of the Processes Involved in the Saturation of Molecular Catalysts 341 Index 347
Gerhard F. Swiegers
Gerhard F. Swiegers
Gerhard F. Swiegers
Gerhard F. Swiegers
Robin Brimblecombe, Jun Chen, Junhua Huang, Ulrich T. Mueller-Westerhoff, and Gerhard F. Swiegers
Robin Brimblecombe, Jun Chen, Junhua Huang, Ulrich T. Mueller-Westerhoff, and Gerhard F. Swiegers
Gerhard F. Swiegers
Gerhard F. Swiegers
Gerhard F. Swiegers
Junhua Huang and Gerhard F. Swiegers
Robin Brimblecombe, G. Charles Dismukes, Greg A. Felton, Leone Spiccia, and Gerhard F. Swiegers
Jun Chen, Junhua Huang, Gerhard F. Swiegers, Chee O. Too, and Gordon G. Wallace
Jun Chen, Gerhard F. Swiegers, Gordon G. Wallace, and Weimin Zhang
Subject Areas: Chemistry [PN]
