Modelling 1H NMR Spectra of Organic Compounds : Theory, Applications and NMR Prediction Software

Provides a theoretical introduction to graduate scientists and industrial researchers towards the understanding of the assignment of 1H NMR spectra Discusses, and includes on enclosed CD, one of the best, the fastest and most applicable pieces of NMR prediction software available Allows students of organic chemistry to solve problems on 1 H NMR with access to over 500 assigned spectra

Preface.Chapter 1: Introduction to 1H NMR.1.1 Historical background.1.2 Basic Theory.1.3 The 1H chemical shift.1.3.1.Nuclear shielding, reference compounds,.1.4. 1H Substituent chemical shifts (SCS).1.4.1. Two-bond effects (H.C.X), Shoolery's rules,.1.4.2. Three-bond effects (H.C.C.X).1.4.3.1H SCS in olefins and aromatics.1.5 Long range effects on 1H chemical shifts.1.5.1. Steric (Van-der-Waals) shifts.1.5.2. electric field and anisotropic shifts.1.5.3. ã electron effects, aromatic ring currents.1.5.4. Hydrogen bonding shifts.1.6.Tables of 1H Chemical Shifts of Common Cyclic Systems.Chapter 2: Interpretation of 1H NMR coupling patterns.2.1 Fine Structure due to HH coupling.2.2 The Analysis of NMR Spectra.2.2.1. Nomenclature of the spin system, chemical and magnetic equivalence.2.2.2. Two interacting nuclei, the AB spectrum.2.2.3. Three interacting nuclei, the ABX spectrum.2.2.4. Four interacting nuclei, the ABRX spectrum, the AA?XX? spectrum.2.2.5. Iterative Computer Analysis, examples.2.3. The Mechanism of Spin-Spin Coupling.2.3.1. Geminal HH Couplings.2.3.2. Vicinal HH Couplings, CH:CH couplings, CH.CH couplings.2.3.3. Ab-initio calculations of couplings.2.3.4. Long-range HH Couplings.2.4. HF Couplings.2.4.1. Geminal HF Couplings.2.4.2. Vicinal HF Couplings, CH:CF couplings, CH.CF couplings.2.4.3. Long-range HF Couplings.Chapter 3: Methods of Predicting 1H Chemical Shifts.3.1. Quantum mechanical calculations of 1H Chemical shifts.3.2. The Data Base Approach, the Hose code.3.3. Semi-empirical calculations,.3.4. Theory of the CHARGE program,.3.4.1 Through Bond Effects.3.4.2 1H Chemical Shifts in Substituted Methanes and Ethanes.3.4.3 Through Space Effects, steric, electric field, magnetic anisotropy.3.4.4Hydrogen Bonding Shifts, ab-initio calculations.3.4.5 Aromatic Compounds, ring currents, ã-electron densities.Chapter 4: Modelling 1H Chemical Shifts, Alkanes,Alkenes and Alkynes.4.1. Alkanes.4.1.1 H..H and C..H steric effects.4.1.2 The methyl effect.4.1.3 C.C Bond Anisotropy.4.1.4 Observed vs Calculated Shifts.a) Acyclic alkanes.b) Cyclic Alkanes.c) Methyl Cycloalkanes.d) Androstane.e) Chemical Shift contributions in Cyclohexane.4.2 Alkenes.4.2.1.C=C Bond Anisotropy and Shielding.4.2.2 Observed vs Calculated Shifts.a) Acyclic alkenes.b) Monocyclic alkenes.c) Aromatic alkenes.d) Norbornenes and bicyclooctenes.e) Pinenes.f) Conclusions.4.3.Alkynes.4.3.1.CðC Bond Anisotropy and Shielding.4.3.2 Observed vs Calculated Shifts.4.3.3. Acetylene SCS.4.3.4. Contributions to Acetylene SCS.4.3.5. Napthyl and Phenanthryl acetylenes.4.4. Summary.Chapter 5: MODELLING 1H CHEMICAL SHIFTS, Aromatics.5.1 Aromatic Hydrocarbons.5.1.1. Ring currents, ã-electron density, steric effects.5.1.2. Observed vs Calculated Shifts.a) Condensed aromatics.b) Cyclophanes.c)Substituted Benzenes.5.2. Heteroaromatics.5.2.1. Theory and Application to Heteroaromatics.5.2.2. Observed vs Calculated Shifts..a) Furans, thiophenes and pyrroles.b) Indoles,quinolines ans isoquinolines.c) Diazabenzenes and azoles.5.2.3. Ring current and ã-electron shifts.5.3. Summary.Chapter 6: MODELLING 1H CHEMICAL SHIFTS, Mono valent Substituents.6.1. Flourocompounds.6.1.1. Electric field theory.6.1.2. Fluoroalkanes.6.1.3. Fluoroalkenes.6.2. Steric,Anisotropic and Electric Field Effects in Chloro,bromo and Iodo SCS.6.2.1. Aromatic h