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• Preface
• Zero & Vacuum: Parallel Stories of Two Parallel Concepts
• Chemical Action & the Transition State Reactivity
• On The Algebraic Chemistry of Catalysis
• Modeling of The Solid-State Polymerization Kinetics
• Dependence of Thermodynamic Characteristics Upon Spatial-Energy Parameter of Free Atoms
• On Chemical Hardness Assessment of Aromaticity for Some Organic Compounds
• A Quantum Mechanical Calculation of The Reactivity Descriptors of Ammonia (NH3) Molecule During The Physical Process of Its Umbrella (C3v --D3h) Inversion & Identification of The Preferred Conformation of Reaction in The Gas Phase
• Computation of Some Descriptors of The Real World in Terms of A New Scale of Electronegativity. Part 1. The Dipole Moments of Some Heteronuclear Diatomic Molecules
• Computation of Some Descriptors of The Real World in Terms of A New Scale of Electronegativity. Part 2. Evaluation of Equilibrium Internuclear Bond Distances of Some Heteronuclear Diatomics
• Density Functional Study on The Stability & Reactivity of Pt(100) & Pt(111) Surfaces Modified by Ni Atoms
• Modeling on Methanol Clusters in Terms of Ab Initio & ABEEM/MM Methods
• Twisted Phenanthrene & Other Molecular Victims of Steric Repulsion
• H-4-Noreudesman-6,12-Olide(-Hydroxy-4-Oxo-11(Molecular Modeling & Spectroscopic Properties of A Sesquiterpene Lactone, 1.
• (source: Nielsen Book Data)

This book presents and discusses current research in the study of chemical modelling. Topics discussed include chemical action and the transition state reactivity; algebraic chemistry of catalysis; solid-state polymerisation kinetics; fractal features of proteins structure and dynamics; modelling on methanol clusters; chemical hardness assessment of aromaticity for certain organic compounds; dependence of thermodynamic characteristics on spatial-energy parameter or free atoms and the scattering of particles and waves on nucleon nodes of the atom.
(source: Nielsen Book Data)

• Metal-Catalyzed Cross-Coupling Reactions
• A Historic Overview of the Metal-Catalyzed Cross-Coupling Reactions / Yaushi Nishihara
• Mechanisms and Fundamental Reactions / Masayuki Iwasaki, Yasushi Nishihara
• Applications of the Cross-Coupling Reactions
• Natural Product Synthesis / Yasuhiro Okuda, Yasushi Nishihara
• Pharmaceuticals / Jiao Jiao, Yasushi Nishihara
• Liquid Crystals / Ning-Hui Chang, Megumi Kinoshita, Yasushi Nishihara
• Conjugated Polymers / Daisuke Ogawa, Yasushi Nishihara
• Recent Advances in Cross-Coupling Reactions
• Recent Advances in Cross-Coupling Reactions with Aryl Chlorides, Tosylates, and Mesylates / Shintaro Noyori, Yasushi Nishihara
• Recent Advances in Cross-Coupling Reactions with Alkyl Halides / Arisa Yamamoto, Yugo Nishimura, Yasushi Nishihara.

""Applied Cross-Coupling Reactions"" provides students and teachers of advanced organic chemistry with an overview of the history, mechanisms and applications of cross-coupling reactions. Since the discovery of the transition-metal-catalyzed cross-coupling reactions in 1972, numerous synthetic uses and industrial applications have been developed. The mechanistic studies of the cross-coupling reactions have disclosed that three fundamental reactions: oxidative addition, transmetalation, and reductive elimination, are involved in a catalytic cycle. Cross-coupling reactions have allowed us to pro

• Chapter 1: Some Milestones in the Development of Surface Chemistry and Catalysis
• 1 Introduction
• 2 1926: Catalysis, Theory and Practice
• Rideal and Taylor
• 3 1932: Adsorption of Gases by Solids
• Faraday Discussion, Oxford
• 4 1940: Seventeenth Faraday Lecture
• Langmuir
• 5 1950: Heterogeneous Catalysis
• Faraday Discussion, Liverpool
• 6 1957: Advances in Catalysis
• International Congress on Catalysis, Philadelphia
• 7 1963: Conference on Clean Surfaces with Supplement: Surface Phenomena in Semiconductors, New York
• 8 1966: Faraday Discussion Meeting, Liverpool
• 9 1967: The Emergence of Photoelectron Spectroscopy
• 10 1968: Berkeley Meeting: Structure and Chemistry of Solid Surfaces
• 11 1972: A Discussion on the Physics and Chemistry of Surfaces, London
• 12 1987: Faraday Symposium, Bath Summary
• References
• Further Reading
• Chapter 2: Experimental Methods in Surface Science Relevant to STM
• 1 Introduction
• 2 Kinetic Methods
• 3 Vibrational Spectroscopy
• 4 Work Function
• 5 Structural Studies
• 6 Photoelectron Spectroscopy
• 7 The Dynamics of Adsorption
• Summary
• References
• Further Reading
• Chapter 3: Scanning Tunnelling Microscopy: Theory and Experiment
• 1 The Development of Ultramicroscopy
• 2 The Theory of STM
• 3 The Interpretation of STM Images
• 4 Scanning Tunnelling Spectroscopy
• 5 The STM Experiment
• 6 The Scanner
• Sample Approach
• Adaptations of the Scanner for Specific Experiments
• 7 Making STM Tips
• Tip Materials
• References
• Chapter 4: Dynamics of Surface Reactions and Oxygen Chemisorption
• 1 Introduction
• 2 Surface Reconstruction and "Oxide" Formation
• 3 Oxygen States at Metal Surfaces
• 4 Control of Oxygen States by Coadsorbates
• 5 Adsorbate Interactions, Mobility and Residence Times
• 6 Atom-tracking STM
• 7 Hot Oxygen Adatoms: How Are They Formed?
• Summary
• References
• Further Reading
• Chapter 5: Catalytic Oxidation at Metal Surfaces: Atom Resolved Evidence
• 1 Introduction
• 2 Ammonia Oxidation
• Cu(110) Pre-exposed to Oxygen
• Coadsorption of Ammonia-Oxygen Mixtures at Cu(110)
• Coadsorption of Ammonia-Oxygen Mixtures at Mg(0001)
• Ni(110) Pre-exposed to Oxygen
• Ag(110) Pre-exposed to Oxygen
• 3 Oxidation of Carbon Monoxide
• 4 Oxidation of Hydrogen
• 5 Oxidation of Hydrocarbons
• 6 Oxidation of Hydrogen Sulfide and Sulfur Dioxide
• 7 Theoretical Analysis of Activation by Oxygen
• Summary
• References
• Further Reading
• Chapter 6: Surface Modification by Alkali Metals
• 1 Introduction
• 2 Infrared Studies of CO at Cu(110)-Cs
• 3 Structural Studies of the Alkali Metal-modified Cu(110) Surfaces
• Low-energy Electron Diffraction
• Scanning Tunnelling Microscopy
• Cu(110)-Cs System
• Oxygen Chemisorption at Cu(110)-Cs
• 4 Reactivity of Cu(110)-Cs to NH3 and CO2
• 5 Au(110)-K System
• 6 Cu(100)-Li System
• Summary
• References
• Further Reading
• Chapter 7: STM at High Pressure
• 1 Introduction
• 2 Catalysis and Chemisorption at Metals at High Pressure
• Carbon Monoxide and Nitric Oxide
• Hydrogenation of Olefins
• 3 Restructuring of the Pt(110)-(1 I 2) Surface by Carbon Monoxide
• 4 Adsorption-induced Step Formation
• 5 Gold Particles at FeO(111)
• 6 Hydrogen-Deuterium Exchange and Surface Poisoning
• Summary
• References
• Further Reading
• Chapter 8: Molecular and Dissociated States of Molecules: Biphasic Systems
• 1 Introduction
• 2 Nitric Oxide
• 3 Nitrogen Adatoms: Surface Structure
• 4 Carbon Monoxide
• 5 Hydrogen
• 6 Dissociative Chemisorption of HCl at Cu(110)
• 7 Chlorobenzene
• 8 Hydrocarbon Dissociation: Carbide Formation
• 9 Dissociative Chemisorption of Phenyl Iodide
• 10 Chemisorption and Trimerization of Acetylene at Pt(111)
• Summary
• References
• Further Reading
• Chapter 9: Nanoparticles and Chemical Reactivity
• 1 Introduction
• 2 Controlling Cluster Size on Surfaces
• 3 Alloy Ensembles
• 4 Nanoclusters at Oxide Surfaces
• 5 Oxidation and Polymerisation at Pd Atoms Deposited on MgO Surfaces
• 6 Clusters in Nanocatalysis
• 7 Molybdenum Sulfide Nanoclusters and Catalytic Hydrodesulfurisation Reaction Pathways
• 8 Nanoparticle Geometry at Oxide-supported Catalysts
• Summary
• References
• Further Reading
• Chapter 10: Studies of Sulfur and Thiols at Metal Surfaces
• 1 Introduction
• 2 Studies of Atomic Sulfur Adsorbed at Metal Surfaces
• Copper
• Nickel
• Gold and Silver
• Platinum, Rhodium, Ruthenium and Rhenium
• Alloy systems
• 3 Sulfur-containing Molecules
• Summary
• References
• Further Reading
• Chapter 11: Surface Engineering at the Nanoscale
• 1 Introduction
• 2 "Bottom-up" Surface Engineering
• Van der Waals Forces
• Hydrogen Bonding
• Chiral Surfaces from Prochiral Adsorbates
• Covalently Bonded Systems
• 3 Surface Engineering Using Diblock Copolymer Templates
• Summary
• References
• Further Reading
• Epilogue
• Catalysis and the Greenhouse Phenomenon
• Subject Index--.
• (source: Nielsen Book Data)

This book offers a unique perspective of the impact of scanning probe microscopes on our understanding of the chemistry of the surface at the nanoscale. Research oriented, with the concepts gleaned from Scanning Tunnelling Microscopy being related to the more established and accepted views in surface chemistry and catalysis, the authors have addressed the question "How do the models based on classical spectroscopic and kinetic studies stand up to scrutiny at the atom-resolved level?". In taking this approach the reader, new to the field of surface chemistry, should be able to obtain a perspective on how the evidence from STM confirms or questions long standing tenets. An emphasis is given to "how did we get to where we are now" and a large number of figures from the literature are included along with suggestions for further reading. Topics discussed include: - the dynamics of oxygen chemisorption at metal surfaces - control of oxygen states and surface reconstruction - dissociative chemisorption of diatomic and hydrocarbon molecules - nanoparticles and chemical reactivity - STM at high pressures - structural studies of sulfur containing molecules and molecular templating This book will appeal to all those who wish to become familiar with the contribution Scanning Tunnelling Microscopy has made to the understanding of the field of surface chemistry and heterogeneous catalysis and also to those who are new to catalysis, a fascinating and important area of chemistry.
(source: Nielsen Book Data)

A century and a half ago the pioneering physicist and chemist Michael Faraday delivered a celebrated series of lectures that attempted to explain the inner workings of matter through the chemical history of a candle. "There is no better, there is no more open door by which you can enter into the study of natural philosophy", Faraday told his audience. Now the distinguished chemist P.W. Atkins follows in Faraday's footsteps, using his predecessor's deceptively simple theme to show how far we have come in understanding the remarkable chemical reactions that govern everything from how candles burn to how life functions. While Faraday could say little more than that a chemical reaction changes a substance's appearance and properties, chemists today understand reactions in terms of the rearrangement of atoms and electrons. Atkins - tracing the course of a carbon atom released by a flaming candle - explores the complex forces that operate at the atomic and sub atomic levels to drive these rearrangements.
(source: Nielsen Book Data)

• 1. Additions to alkenes, alkynes, and carbonyl compounds / authors, R. Ballini [and 25 others]
• 2. Alkenations, cross couplings, insertions, substitutions, and halomethylations / authors, R. Ballini [and 33 others].

• Contributors xi Preface xiii
• 1 Amine-Catalyzed Cascade Reactions 1 Aiguo Song and Wei Wang 1.1 Introduction, 2 1.2 Enamine-Activated Cascade Reactions, 3 1.2.1 Enamine Enamine Cascades, 3 1.2.2 Enamine Iminium Cascades, 8 1.2.3 Enamine Catalysis Cyclization, 19 1.3 Iminium-Initiated Cascade Reactions, 21 1.3.1 Design of Iminium Enamine Cascade Reactions, 21 1.3.2 Iminium-Activated Diels Alder Reactions, 22 1.3.3 Iminium-Activated Sequential [4 + 2] Reactions, 24 1.3.4 Iminium-Activated [3 + 2] Reactions, 25 1.3.5 Iminium-Activated Sequential [3 + 2] Reactions, 27 1.3.6 Iminium-Activated [2 + 1] Reactions, 30 1.3.7 Iminium-Activated Multicomponent Reactions, 35 1.3.8 Iminium-Activated [3 + 3] Reactions, 37 1.4 Cycle-Specific Catalysis Cascades, 42 1.5 Other Strategies, 45 1.6 Summary and Outlook, 46 References, 46
• 2 Bronsted Acid Catalyzed Cascade Reactions 53 Jun Jiang and Liu-Zhu Gong 2.1 Introduction, 54 2.2 Protonic Acid Catalyzed Cascade Reactions, 55 2.2.1 Mannich Reaction, 55 2.2.2 Pictect Spengler Reaction, 56 2.2.3 Biginelli Reaction, 58 2.2.4 Povarov Reaction, 59 2.2.5 Reduction Reaction, 60 2.2.6 1,3-Dipolar Cycloaddition, 61 2.2.7 Darzen Reaction, 65 2.2.8 Acyclic Aminal and Hemiaminal Synthesis, 66 2.2.9 Rearrangement Reaction, 67 2.2.10 a, b-Unsaturated Imine-Involved Cyclization Reaction, 69 2.2.11 Alkylation Reaction, 69 2.2.12 Desymmetrization Reaction, 70 2.2.13 Halocyclization, 71 2.2.14 Redox Reaction, 72 2.2.15 Isocyanide-Involved Multicomponent Reaction, 73 2.2.16 Other Protonic Acid Catalyzed Cascade Reactions, 75 2.3 Chiral Thiourea (Urea) Catalyzed Cascade Reactions, 75 2.3.1 Neutral Activation, 76 2.3.2 Anion-Binding Catalysis, 99 2.4 Bronsted Acid and Transition Metal Cooperatively Catalyzed Cascade Reactions, 104 2.4.1 Dual Catalysis, 105 2.4.2 Cascade Catalysis, 108 2.5 Conclusions, 116 References, 117
• 3 Application of Organocatalytic Cascade Reactions in Natural Product Synthesis and Drug Discovery 123 Yao Wang and Peng-Fei Xu 3.1 Introduction, 123 3.2 Amine-Catalyzed Cascade Reactions in Natural Product Synthesis, 125 3.2.1 Iminium-Ion-Catalyzed Cascade Reactions in Natural Product Synthesis, 125 3.2.2 Cycle-Specific Cascade Catalysis in Natural Product Synthesis, 129 3.3 Bronsted Acid Catalyzed Cascade Reactions in Natural Product Synthesis, 137 3.4 Bifunctional Base/Bronsted Acid Catalyzed Cascade Reactions in Natural Product Synthesis, 139 3.5 Summary and Outlook, 140 References, 142
• 4 Gold-Catalyzed Cascade Reactions 145 Yanzhao Wang and Liming Zhang 4.1 Introduction, 145 4.2 Cascade Reactions of Alkynes, 147 4.2.1 Cascade Reactions of Enynes, 147 4.2.2 Cascade Reactions of Propargyl Carboxylates, 156 4.2.3 Cascade Reactions of ortho-Substituted Arylalkynes, 161 4.2.4 Cascade Reactions of Other Alkynes, 165 4.3 Cascade Reactions of Allenes, 170 4.4 Cascade Reactions of Alkenes and Cyclopropenes, 173 4.5 Closing Remarks, 174 References, 174
• 5 Cascade Reactions Catalyzed by Ruthenium, Iron, Iridium, Rhodium, and Copper 179 Yanguang Wang and Ping Lu 5.1 Introduction, 179 5.2 Ruthenium-Catalyzed Transformations, 180 5.3 Iron-Catalyzed Transformations, 185 5.4 Iridium-Catalyzed Transformations, 191 5.5 Rhodium-Catalyzed Transformations, 194 5.6 Copper-Catalyzed Transformations, 202 5.7 Miscellaneous Catalytic Reactions, 215 5.8 Summary, 219 References, 219
• 6 Palladium-Catalyzed Cascade Reactions of Alkenes, Alkynes, and Allenes 225 Hongyin Gao and Junliang Zhang 6.1 Introduction, 226 6.2 Cascade Reactions Involving Alkenes, 226 6.2.1 Double Mizoroki Heck Reaction Cascade, 226 6.2.2 Cascade Heck Reaction/C-H Activation, 227 6.2.3 Cascade Heck Reaction/Reduction/Cyclization, 230 6.2.4 Cascade Heck Reaction/Carbonylation, 231 6.2.5 Cascade Heck Reaction/Suzuki Coupling, 232 6.2.6 Cascade Amino-/Oxopalladation/Carbopalladation Reaction, 234 6.3 Cascade Reactions Involving Alkynes, 237 6.3.1 Cascade Heck Reactions, 238 6.3.2 Cascade Heck/Suzuki Coupling, 238 6.3.3 Cationic Palladium(II)-Catalyzed Cascade Reactions, 239 6.3.4 Cascade Heck Reaction/Stille Coupling, 241 6.3.5 Cascade Heck/Sonogashira Coupling, 243 6.3.6 Cascade Sonogashira Coupling Cyclization, 244 6.3.7 Cascade Heck and C-H Bond Functionalization, 247 6.3.8 Cascade Reactions Initiated by Oxopalladation, 253 6.3.9 Cascade Reactions Initiated by Aminopalladation, 256 6.3.10 Cascade Reactions Initiated by Halopalladation or Acetoxypalladation, 259 6.3.11 Cascade Reactions of 2-(1-Alkynyl)-alk-2-en-1-ones, 263 6.3.12 Cascade Reactions of Propargylic Derivatives, 263 6.4 Cascade Reactions Involving Allenes, 264 6.4.1 Cascade Reactions of Monoallenes, 264 6.4.2 Cross-Coupling Cyclization of Two Different Allenes, 274 6.5 Summary and Outlook, 276 Acknowledgments, 277 References, 277
• 7 Use of Transition Metal Catalyzed Cascade Reactions in Natural Product Synthesis and Drug Discovery 283 Peng-Fei Xu and Hao Wei 7.1 Introduction, 283 7.2 Palladium-Catalyzed Cascade Reactions in Total Synthesis, 284 7.2.1 Cross-Coupling Reactions, 284 7.2.1.1 Heck Reaction, 284 7.2.1.2 Stille Reaction, 291 7.2.1.3 Suzuki Coupling Reaction, 297 7.2.2 Tsuji Trost Reaction, 301 7.2.3 Other Palladium-Catalyzed Cascade Reactions in Total Synthesis, 303 7.3 Ruthenium-Catalyzed Cascade Reactions in Total Synthesis, 305 7.4 Gold-and Platinum-Catalyzed Cascade Reactions in Organic Reactions, 318 7.5 Copper-and Rhodium-Catalyzed Cascade Reactions in Organic Synthesis, 322 7.6 Summary, 326 References, 326
• 8 Engineering Mono-and Multifunctional Nanocatalysts for Cascade Reactions 333 Hexing Li and Fang Zhang 8.1 Introduction, 334 8.2 Heterogeneous Monofunctional Nanocatalysts, 335 8.2.1 Metal-Based Monofunctional Nanocatalysts, 335 8.2.2 Metal Oxide Based Monofunctional Nanocatalysts, 340 8.2.3 Orgamometallic-Based Monofunctional Nanocatalysts, 340 8.2.4 Graphene Oxide Based Monofunctional Nanocatalysts, 343 8.3 Heterogeneous Multifunctional Nanocatalysts, 344 8.3.1 Acid Base Combined Multifunctional Nanocatalysts, 344 8.3.2 Metal Base Combined Multifunctional Nanocatalysts, 349 8.3.3 Organometallic Base Combined Multifunctional Nanocatalysts, 349 8.3.4 Binary Organometallic Based Multifunctional Nanocatalysts, 350 8.3.5 Binary Metal Based Multifunctional Nanocatalysts, 352 8.3.6 Metal Metal Oxide Combined Multifunctional Nanocatalysts, 353 8.3.7 Organocatalyst Acid Combined Multifunctional Nanocatalysts, 353 8.3.8 Acid Base Metal Combined Multifunctional Nanocatalyst, 356 8.3.9 Triple Enzyme Based Multifunctional Nanocatalysts, 356 8.4 Conclusions and Perspectives, 359 References, 360
• 9 Multiple-Catalyst-Promoted Cascade Reactions 363 Peng-Fei Xu and Jun-Bing Ling 9.1 Introduction, 363 9.2 Multiple Metal Catalyst Promoted Cascade Reactions, 364 9.2.1 Catalytic Systems Involving Palladium, 365 9.2.2 Catalytic Systems Involving Other Metals, 368 9.3 Multiple Organocatalyst Promoted Cascade Reactions, 370 9.3.1 Catalytic Systems Combining Multiple Amine Catalysts, 371 9.3.2 Catalytic Systems Combining Amine Catalysts and Nucleophilic Carbenes, 380 9.3.3 Catalytic Systems Combining Amine and Hydrogen-Bonding Donor Catalysts, 385 9.3.4 Catalytic Systems Involving Other Organocatalysts, 390 9.4 Metal/Organic Binary Catalytic System Promoted Cascade Reactions, 394 9.4.1 Catalytic Systems Combining Secondary Amine and Metal Catalysts, 394 9.4.2 Catalytic Systems Combining Bronsted Acid and Metal Catalysts, 404 9.4.3 Catalytic Systems Combining Hydrogen-Bonding Donor and Metal Catalysts, 411 9.4.4 Catalytic Systems Combining Other Organo-and Metal Catalysts, 413 9.5 Summary and Outlook, 415 References, 415 Index 419.
• (source: Nielsen Book Data)

The development of catalytic versions of cascade reactions has become one of the most active and burgeoning reaction areas in organic synthesis. Covering both organocatalysis and transition-metal catalysis for these reactions, Catalytic Cascade Reactions illustrates the versatility and application of cascade reactions for synthesizing valuable compounds, such as drugs and natural products. Highlighting catalytic versus non-catalytic reactions, an important shift in academic and industry practice, the text brings chemists and the organic synthesis community up to speed on the many recent advances in the field.
(source: Nielsen Book Data)

• Synthesis in the Key of Catellani: Norbornene-Mediated ortho C-H Functionalization.- Mechanistic Considerations in the Development and Use of Azine, Diazine and Azole N-Oxides in Palladium-Catalyzed Direct Arylation.- Palladium and Copper Catalysis in Regioselective, Intermolecular Coupling of C-H and C-Hal Bonds.- Pd-Catalyzed C-H Bond Functionalization on the Indole and Pyrrole Nucleus.- Remote C-H Activation via Through-Space Palladium and Rhodium Migrations.- Palladium-Catalyzed Aryl-Aryl Bond Formation Through Double C-H Activation.- Palladium-Catalyzed Allylic C-H Bond Functionalization of Olefins.- Ruthenium-Catalyzed Direct Arylations Through C-H Bond Cleavages.- Rhodium-Catalyzed C-H Bond Arylation of Arenes.- Cross-Dehydrogenative Coupling Reactions of sp3-Hybridized C-H Bonds.- Functionalization of Carbon-Hydrogen Bonds Through Transition Metal Carbenoid Insertion.- Metal-Catalyzed Oxidations of C-H to C-N Bonds.
• (source: Nielsen Book Data)

Table of Contents - Synthesis in the Key of Catellani: Norbornene-Mediated ortho C-H Functionalization - Mechanistic Considerations in the Development and Use of Azine, Diazine and Azole N-Oxides in Palladium-Catalyzed Direct Arylation - Palladium and Copper Catalysis in Regioselective, Intermolecular Coupling of C-H and C-Hal Bonds - Pd-Catalyzed C-H Bond Functionalization on the Indole and Pyrrole Nucleus - Remote C-H Activation via Through-Space Palladium and Rhodium Migrations - Palladium-Catalyzed Aryl-Aryl Bond Formation Through Double C-H Activation - Palladium-Catalyzed Allylic C-H Bond Functionalization of Olefins - Ruthenium-Catalyzed Direct Arylations Through C-H Bond Cleavages - Rhodium-Catalyzed C-H Bond Arylationof Arenes - Cross-Dehydrogenative Coupling Reactions of sp3-Hybridized C-H Bonds - Functionalization of Carbon-Hydrogen Bonds Through Transition Metal Carbenoid Insertion - Metal-Catalyzed Oxidations of C-H to C-N Bonds.
(source: Nielsen Book Data)

• Magentic scenario of chemical reaction
• magnetic interactions in chemical reactions
• magnetic effects in chemical reactions
• chemically induced radio-frequency emission
• reaction yield detected magnetic resonance - RYDMR
• RYDMR in solids
• RYDMR in liquid solutions
• RYDMR in photosynthetic systems
• radio-induced magnetic isotope effect
• microwave-stimulated nuclear polarization
• coherence in spin dynamics and chemical reactivity
• on the action of electromagnetic waves on biological processes.
• (source: Nielsen Book Data)

Covering the fields of chemical kinetics, theoretical chemistry and metabolite chemistry, this work considers the chemical generation and reception of radio- and microwaves.
(source: Nielsen Book Data)
An overview of spin chemistry and chemical physics. This text should be useful reading for chemical physicists, physical organic chemists, materials scientists, and radio- and biophysicists.
(source: Nielsen Book Data)