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Organic

Most popular at the top

  • Electro-Optics and Dielectrics of Macromolecules and Colloidsby

    Springer US 2012; US$ 99.00

    Theoretical Advances.- Specific Kerr Constants of Rigid, Ellipsoidal Macromolecules in Conducting Solution at Very Low Ionic Strength.- Transient Electric Birefringence of Macromolecular Solutions at Reversing Fields of Arbitrary Strength and Duration.- The Limit of the Numerical Method of Inverting the Laplace Transformation and the Uniqueness of... more...

  • Elements of Organic Photochemistryby

    Springer US 2012; US$ 99.00

    1 Basic Photophysical and Photochemical Concepts.- 1.1. Introduction.- 1.2. Energy Distribution in the Excited Molecule.- 1.2a. Light Absorption.- 1.2b. Internal Conversion and Intersystem Crossing.- 1.2c. Fluorescence and Phosphorescence.- 1.3. Photochemical Kinetics: Concentrations, Rates, Yields, and Quantum Yields.- 1.4. Classification of Molecular... more...

  • Neighboring Group Participationby

    Springer US 2012; US$ 99.00

    1. General Considerations.- 1. Introduction.- 1.1. Historical and General Description of Neighboring Group Effects.- 1.2. Terms and Definitions.- 2. Some Factors that Influence Anchimeric Assistance.- 2.1. The Stabilities of Bridged Carbocations?Some Molecular Orbital Calculations.- 2.2 Hyperconjugation?An Alternative Explanation?.- 2.3. The Effect... more...

  • Carbon-13 NMR Shift Assignments of Amines and Alkaloidsby M. Shamma

    Springer US 2012; US$ 99.00

    1. Pyrroles.- 2. Pyrrolidines.- 3. Retrorsine: A Pyrrolizidine Alkaloid.- 4. Pyridines.- 5. Piperidines.- 6. Simple Enamines.- 7. Tropanes.- 8. Quinolizidines.- a. Simple Quinolizidines.- b. Julolidines.- c. Matrines.- d. Sparteines.- e. Nuphar Alkaloids.- f. Lycopodium Alkaloids.- 9. Quinolines.- a. Simple Quinolines.- b. Quinolones.- c. Reduced Quinolines.-... more...

  • The PMO Theory of Organic Chemistryby Michael Dewar

    Springer US 2012; US$ 99.00

    1. Introduction to MO Theory.- 1.1. The Hydrogen Atom; Orbits and Orbitals.- 1.2. The Orbital Approximation; Helium.- 1.3. Lithium; the Pauli Principle.- 1.4. The Atoms Be-Ne; Hund?s Rule.- 1.5. The Hydrogen Molecule; Molecular Orbitals.- 1.6. The Born-Oppenheimer Approximation.- 1.7. HHe +, HHe, and HLi; Perturbation Theory.- 1.8. Methane; Symmetry... more...

  • The PMO Theory of Organic Chemistryby Michael Dewar

    Springer US 2012; US$ 99.00

    1. Introduction to MO Theory.- 1.1. The Hydrogen Atom; Orbits and Orbitals.- 1.2. The Orbital Approximation; Helium.- 1.3. Lithium; the Pauli Principle.- 1.4. The Atoms Be-Ne; Hund?s Rule.- 1.5. The Hydrogen Molecule; Molecular Orbitals.- 1.6. The Born-Oppenheimer Approximation.- 1.7. HHe+, HHe, and HLi; Perturbation Theory.- 1.8. Methane; Symmetry... more...

  • Organotransition-Metal Chemistryby

    Springer US 2012; US$ 99.00

    Synthesis of Organotransition Metals.- Metallocarboranes: Past, Present, and Future.- Novel Rhodium and Palladium Complexes with Benzoyl and Thiobenzoyl Isocyanates as Ligands.- Polycyanovinyl Transition Metal Derivatives.- A New Preparation of Organocopper(I)-Isonitrile Complexes and Their Reactions.- An Unusual Behavior of ?-Vinyl Alcohol Complexes... more...

  • Polychloroaromatic Compoundsby

    Springer US 2012; US$ 99.00

    1 Aromatic and Alkaromatic Chlorocarbons.- 2 Polychloroheteroaromatic Compounds.- 3 Polychloroaryl Derivatives of Metals and Metalloids.- 4 Polychloroaromatics and Heteroaromatics of Industrial Importance.- Author Index. more...

  • Physical Chemistry of Organic Solvent Systemsby

    Springer US 2012; US$ 99.00

    1 Introduction and Solvent Properties.- 2 Thermodynamic Measurements.- 1 Solubility, Calorimetry, Volume Measurements and Viscosities.- 2 Electrochemical Measurements.- 3 Precision Cryoscopy.- 4 Interpretation of Thermodynamic Data.- 3 Acid-base Behaviour.- 4 Spectroscopic Measurements.- 1 Electronic Absorption Spectroscopy.- 2 Infrared and Raman Spectroscopy.-... more...

  • Protective Groups in Organic Chemistryby

    Springer US 2012; US$ 99.00

    1 Protection of C-H Bonds.- 2 Protection of N-H Bonds and NR3.- 3 Protection of Alcholic Hydroxyl Groups and Glycols Systems.- 4 Protection of Phenols and Catechols.- 5 Protection of Carboxyl Groups.- 6 Protection of Phosphoric and Related Acids.- 7 Protection of Thiols.- 8 Protection of Carbon-Carbon Multiple Bonds.- 9 Protection of Aldehydes and... more...