Collision Theory and Statistical Theory of Chemical Reactions. (= Lecture Notes in Chemistry - Volume 18).

Christov, Stefan G.:

ISBN 10: 3540100121 / ISBN 13: 9783540100126

Editore: Springer, Berlin, 1980

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322 S., 3540100121 Sprache: Englisch Gewicht in Gramm: 540 Groß 8°, (large 8vo), Original-Karton (Softcover), Bibliotheks-Exemplar mit Rückenschild, Stempel auf Vorsatz, Titel, Schnitt und Innendeckel, Ecken und Kanten leicht berieben, Deckel mit kleiner Schabspur, insgesamt gutes und innen sauberes Exemplar, (library copy in alltogether good condition),

Codice articolo 57662

Dati bibliografici

• Titolo: Collision Theory and Statistical Theory of Chemical Reactions. (= Lecture Notes in Chemistry - Volume 18).
• Editore: Springer, Berlin
• Data di pubblicazione: 1980
• Lingua: Inglese
• ISBN 10: 3540100121
• ISBN 13: 9783540100126
• Rilegatura: Brossura
• Peso: 540 grammi
• Cataloghi dei venditori:
  • Chemie

Descrizione articolo

Riassunto

Since the discovery of quantum mechanics,more than fifty years ago,the theory of chemical reactivity has taken the first steps of its development. The knowledge of the electronic structure and the properties of atoms and molecules is the basis for an un­ derstanding of their interactions in the elementary act of any chemical process. The increasing information in this field during the last decades has stimulated the elaboration of the methods for evaluating the potential energy of the reacting systems as well as the creation of new methods for calculation of reaction probabili­ ties (or cross sections) and rate constants. An exact solution to these fundamental problems of theoretical chemistry based on quan­ tum mechanics and statistical physics, however, is still impossible even for the simplest chemical reactions. Therefore,different ap­ proximations have to be used in order to simplify one or the other side of the problem. At present, the basic approach in the theory of chemical reactivity consists in separating the motions of electrons and nu­ clei by making use of the Born-Oppenheimer adiabatic approximation to obtain electronic energy as an effective potential for nuclear motion. If the potential energy surface is known, one can calculate, in principle, the reaction probability for any given initial state of the system. The reaction rate is then obtained as an average of the reaction probabilities over all possible initial states of the reacting ~artic1es. In the different stages of this calculational scheme additional approximations are usually introduced.

Contenuti

Historical Introduction.- I The Potential Energy of Reactive Systems.- 1. The Adiabatic Approximation.- 2. Corrections to the Adiabatic Approximation.- 3. Potential Energy Surfaces.- 3.1. Calculation of the Electronic Surfaces.- 3.2. Correlation between Chemical Reactivity and Electronic Structure (or Electronic State).- II Dynamics of Molecular Collisions.- 1. General Considerations.- 1.1. Separation of Nuclear Motions.- 1.2. Time-Dependent and Time-Independent Collision Theory.- 2. Transition Probability and Cross Section.- 3. Classical Trajectory Calculations.- 4. Quantum-Mechanical Calculations.- 4.1. One-Dimensional Consideration.- 4.2. Many-Dimensional Consideration.- 5. Quasi-Classical Calculations.- 6. Non-Adiabatic Transitions in Chemical Reactions.- 6.1. Semiclassical Consideration.- 6.2. Quantum-Mechanical Consideration.- III General Theory of Reaction Rates.- 1. Basic Assumptions.- 2. Collision Theory Formulation of Reaction Rates.- 3. “Statistical” Formulation of Reaction Rates.- 4. Classical and Semiclassical Approximations to the Rate Equations.- 4.1. Collision Theory Treatment.- 4.2. Statistical Theory Treatment.- 5. Adiabatic Statistical Theory of Reaction Rates.- 5.1. Exact Formulation of the Adiabatic Theory.- 5.2. Approximate Equations of the Adiabatic Theory.- 6. Evaluation of the Transmission Coefficient and the Tunneling Correction.- 6.1. General Remarks.- 6.2. Evaluation of the Transmission Coefficient.- 6.3. Evaluation of the Tunneling Correction.- 6.3.1. One-Dimensional Treatment.- 6.3.2. Many-Dimensional Treatment.- 7. General Consequences from the Rate Equations.- 7.1. Basic Relations.- 7.2. Effective Activation Energy and Collision (Frequency) Factor.- 7.3. Effective Activation Energy, Rate Constant and Reaction Heat.- 7.4. Kinetic Isotope Effects.- IV Applications of Reaction Rate Theory.- 1. General Considerations.- 2. Gas Phase Reactions.- 2.1. Unimolecular Reactions.- 2.1.1. General Remarks.- 2.1.2. Collision Theory Treatment.- 2.1.3. Statistical Treatment.- 2.2. Bimolecular Reactions.- 2.2.1. General Remarks.- 2.2.2. Collision Theory Treatment.- 2.2.3. Statistical Treatment.- 2.2.4. Calculations of the Correction Factors H and Hac for the Isotopic H + H2 Reactions.- 2.2.5. Calculations of the Rate Constants and Arrhenius Parameters of the Isotopic H2+ H Reactions.- 3. Dense Phase Reactions.- 3.1. General Remarks.- 3.2. Redox Reactions.- 3.3. Proton-Transfer Reactions in Solution.- 3.4. Electrode Reactions.- 3.5. Biochemical Reactions.- Concluding Remarks.- References.