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Advances in physical organic chemistry. Volume 52 /

Detalles Bibliográficos
Clasificación:Libro Electrónico
Otros Autores: Williams, Ian (Editor ), Williams, Nick (Editor )
Formato: Electrónico eBook
Idioma:Inglés
Publicado: London, United Kingdom : Academic Press, 2018.
Colección:Advances in Physical Organic Chemistry Ser.
Temas:
Acceso en línea:Texto completo

MARC

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245 0 0 |a Advances in physical organic chemistry.  |n Volume 52 /  |c edited by Ian H. Williams, Nicholas H. Williams. 
264 1 |a London, United Kingdom :  |b Academic Press,  |c 2018. 
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490 1 |a Advances in Physical Organic Chemistry Ser. ;  |v v. Volume 52 
588 0 |a Online resource; title from PDF title page (ScienceDirect, viewed November 26, 2018). 
505 0 |a Front Cover; Advances in Physical Organic Chemistry; Copyright; Contents; Contributors; Preface; Chapter One: The Conundrum of the (C4H7)+ Cation: Bicyclobutonium and Related Carbocations; 1. Introduction; 1.1. Early Studies; 1.2. Terminology; 1.3. Kinetic Isotope Effects; 1.4. Gas-Phase Studies; 1.5. Vibrational Spectroscopy; 1.6. Structures and Equilibrium of Bicyclobutonium and Cyclopropylmethyl Cations; 1.7. NMR Spectroscopic Investigations; 1.8. EIEs on NMR Spectra of Fast-Rearranging (C4H7)+ Cations; 1.9. Quantum-Chemical Calculations of EIEs in (C4H7)+ Cations. 
505 8 |a 1.9.1. The Size and the Direction of the EIEs1.9.2. Population of the Equilibrating Sites; 1.9.3. The Size of the EIE; 1.9.4. The EIE-Induced Direction of the NMR Chemical Shifts of the Averaged Methylene Signals; 1.9.5. Quantum-Chemical Calculations for the (C4H7)+ Cation System; 2. Substituted (C4H7)+ Carbocations; 2.1. Fast-Equilibrating Substituted Bicyclobutonium Ions; 2.1.1. Solvolysis Results of Substituted Cyclobutyl Derivatives; 2.2. NMR Spectroscopic and Computational Investigations of Substituted (C4H7)+ Cations; 2.2.1. 1-Methyl-Bicyclobutonium Cation. 
505 8 |a 2.2.2. The 1-(Trimethylsilyl)Bicyclobutonium Ion2.3. EIEs in Substituted Cyclopropylmethyl and Substituted Cyclobutyl Cations; 2.4. Static Substituted Bicyclobutonium Ions; 2.5. Spin-Spin Coupling Constants; 2.6. 1,3-Disubstituted Static Bicyclobutonium Ions; 3. Conclusion; References; Chapter Two: Organic Reaction Outcomes in Ionic Liquids; 1. Introduction; 1.1. Scope of This Review; 1.2. Ionic Liquids: Common Structures and Nomenclature; 2. Understanding Reaction Outcomes in Ionic Liquids: Key Milestones; 2.1. Not All Ionic Liquids Are Created Equal. 
505 8 |a 2.2. The Importance of the Proportion of the Ionic Liquid in the Reaction Mixture2.3. Understanding the Microscopic Origins of Ionic Liquid Effects; 2.4. Correlating Reaction Outcomes With Solvent Parameters; 3. Opportunities Delivered by the Understanding Gained; 3.1. Extending the Knowledge to Other Systems; 3.2. Rational Design of an Ionic Liquid Solvent; 3.3. Biasing Product Selectivity; 4. Summary and Outlook; Acknowledgments; References; Chapter Three: Polymer Mechanochemistry: A New Frontier for Physical Organic Chemistry; 1. Introduction. 
505 8 |a 2. A Quantitative Model of Mechanochemical Kinetics2.1. Approximate Solutions of the Master Equation of Mechanochemical Kinetics; 2.1.1. Zeroth-Order Approximation: The EB Model; 2.1.2. First-Order Approximation: Tilted Potential Energy Surface (TPES) and Cusp Models; 2.1.3. Second-Order and Complete Harmonic Approximations; 2.2. Accuracy of the Conventional Approximations and Systematic Strategies of Improving Them; 2.3. Complicating Factors: Ensemble Effects, the Minimum Length of the Macromolecular Segment, Multibarrier Reactions, an ... 
650 0 |a Physical organic chemistry. 
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650 7 |a Physical organic chemistry  |2 fast  |0 (OCoLC)fst01715687 
650 7 |a Fisico-Quimica (Organica)  |2 larpcal 
700 1 |a Williams, Ian,  |e editor. 
700 1 |a Williams, Nick,  |e editor. 
776 0 8 |i Print version:  |a Gold, V.  |t Advances in physical organic chemistry.  |d London : Academic Press, 1969-  |z 9780128152119  |w (OCoLC)37236247 
830 0 |a Advances in Physical Organic Chemistry Ser. 
856 4 0 |u https://sciencedirect.uam.elogim.com/science/bookseries/00653160/52  |z Texto completo