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Nuclear Magnetic Resonance Spectroscopy de Joseph B Lambert

Nuclear Magnetic Resonance Spectroscopy

Autor Joseph B Lambert, Eugene P Mazzola, Clark D Ridge
en Limba Engleză Hardback – 11 ian 2019

Structura și metodologia acestei a doua ediții a Nuclear Magnetic Resonance Spectroscopy sunt concepute pentru a susține un curs universitar complet, oferind un echilibru între rigoarea teoretică necesară specialiștilor și abordarea practică solicitată de chimiștii sinteticieni. Remarcăm organizarea progresivă a materialului, care debutează cu bazele analitice ale rezonanței magnetice nucleare și avansează spre complexitatea sistemelor multi-puls și multi-dimensionale. Subliniem faptul că autorii Joseph B Lambert, Eugene P Mazzola și Clark D Ridge au integrat în text nu doar teorie, ci și sfaturi practice esențiale pentru execuția experimentelor, inclusiv parametri tehnici specifici precum timpii de relaxare și ciclarea fazelor. Considerăm că relevanța acestui volum pentru curriculumul de chimie și biochimie este susținută de includerea unui capitol extins de elucidare structurală, unde o problemă complexă este rezolvată pas cu pas, ilustrând aplicabilitatea tehnicilor discutate. Cititorii familiarizați cu NMR and Chemistry de J.W. Akitt vor aprecia în acest volum detalierea parametrilor experimentali concreți — cum ar fi numărul de scanări sau timpii de mixare — elemente care transformă textul dintr-o expunere teoretică într-un ghid de laborator veritabil. În timp ce alte lucrări se concentrează pe o abordare non-matematică, ediția de față menține standardul academic prin anexe ce utilizează operatori de produs și diagrame de nivel de coerență, oferind astfel o înțelegere profundă a mecanismelor din spatele semnalelor RMN. Este o resursă care acoperă atât nucleele clasice (proton, carbon-13), cât și metodele moderne de procesare a datelor necesare în cercetarea farmaceutică și criminalistică.

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Specificații

ISBN-13: 9781119295235
ISBN-10: 1119295238
Pagini: 480
Dimensiuni: 172 x 251 x 32 mm
Greutate: 1.06 kg
Ediția:2nd edition
Editura: Wiley
Locul publicării:Chichester, United Kingdom

Public țintă

Students and post graduate students working in analytical and bio sciences, as well as scientists who use NMR spectroscopy as a primary tool in their work, e.g. biochemistry, pharmaceutical sciences, forensic sciences, medical imaging,

De ce să citești această carte

Recomandăm această ediție studenților și cercetătorilor care au nevoie de o punte între teoria pură și practica de laborator. Spre deosebire de manualele introductive, volumul oferă setări experimentale detaliate și probleme rezolvate ce reflectă fluxul real de lucru în elucidarea structurilor organice și anorganice. Este un instrument esențial pentru stăpânirea tehnicilor RMN 1D și 2D în chimia modernă.

Despre autor

Joseph B. Lambert, Eugene P. Mazzola și Clark D. Ridge sunt experți recunoscuți în domeniul spectroscopiei, cu o vastă experiență academică și practică. Joseph B. Lambert este o figură proeminentă în chimia organică, cunoscut pentru contribuțiile sale la studiul structurilor moleculare prin metode fizice. Co-autorii săi aduc expertiză suplimentară în aplicațiile biochimice și farmaceutice ale RMN, reușind să creeze un text care reflectă evoluțiile tehnologice recente ale spectrometrelor Fourier transform și ale metodelor de procesare a datelor prin microcomputere, esențiale în laboratoarele moderne de cercetare.

Notă biografică

Joseph B. Lambert, Ph.D., is Research Professor of Chemistry at Trinity University. Eugene P. Mazzola, Ph.D., is an adjunct professor of chemistry at the University of Maryland as well as a researcher at the UMD-FDA Joint Institute for Food Safety and Applied Nutrition. Clark D. Ridge, Ph.D., is an NMR spectroscopist based at the Health and Human Sciences division of the FDA at College Park, Maryland.

Descriere scurtă

Combines clear and concise discussions of key NMR concepts with succinct and illustrative examples Designed to cover a full course in Nuclear Magnetic Resonance (NMR) Spectroscopy, this text offers complete coverage of classic (one-dimensional) NMR as well as up-to-date coverage of two-dimensional NMR and other modern methods. It contains practical advice, theory, illustrated applications, and classroom-tested problems; looks at such important ideas as relaxation, NOEs, phase cycling, and processing parameters; and provides brief, yet fully comprehensible, examples. It also uniquely lists all of the general parameters for many experiments including mixing times, number of scans, relaxation times, and more. Nuclear Magnetic Resonance Spectroscopy: An Introduction to Principles, Applications, and Experimental Methods, 2nd Edition begins by introducing readers to NMR spectroscopy - an analytical technique used in modern chemistry, biochemistry, and biology that allows identification and characterization of organic, and some inorganic, compounds. It offers chapters covering: Experimental Methods; The Chemical Shift; The Coupling Constant; Further Topics in One-Dimensional NMR Spectroscopy; Two-Dimensional NMR Spectroscopy; Advanced Experimental Methods; and Structural Elucidation. * Features classical analysis of chemical shifts and coupling constants for both protons and other nuclei, as well as modern multi-pulse and multi-dimensional methods * Contains experimental procedures and practical advice relative to the execution of NMR experiments * Includes a chapter-long, worked-out problem that illustrates the application of nearly all current methods * Offers appendices containing the theoretical basis of NMR, including the most modern approach that uses product operators and coherence-level diagrams By offering a balance between volumes aimed at NMR specialists and the structure-determination-only books that focus on synthetic organic chemists, Nuclear Magnetic Resonance Spectroscopy: An Introduction to Principles, Applications, and Experimental Methods, 2nd Edition is an excellent text for students and post-graduate students working in analytical and bio-sciences, as well as scientists who use NMR spectroscopy as a primary tool in their work.

Cuprins

Preface to First Edition
Preface to Second Edition
Symbols
Abbreviations
1. Introduction
1.1. Magnetic Properties of Nuclei
1.2. The Chemical Shift
1.3. Excitation and Relaxation
1.4. Pulsed Experiments
1.5. The Coupling Constant
1.6. Quantitation and Complex Splitting
1.7. Commonly Studied Nuclides
1.8. Dynamic Effects
1.9. Spectra of Solids
Problems
Tips on Solving NMR Problems
Bibliography
2. Introductory Experimental Methods
2.1. The Spectrometer
2.2. Sample Preparation
2.3. Optimizing the Signal
2.3a. Sample Tube Placement
2.3b. Probe Tuning
2.3c. Field/Frequency Locking
2.3d. Spectrometer Shimming
2.4. Determination of NMR Spectra-Acquisition Parameters
2.4a. Number of Data Points
2.4b. Spectral Width
2.4c. Filter Bandwidth
2.4d. Acquisition Time
2.4e. Transmitter Offset
2.4f. Flip Angle
2.4g. Receiver Gain
2.4h. Number of Scans
2.4i. Steady-State Scans
2.4j. Oversampling and Digital Filtration
2.4k. Decoupling for X Nuclei
2.4l. Typical NMR Experiments
2.5. Determination of NMR Spectral-Processing Parameters
2.5a. Exponential Weighting
2.5b. Zero Filling
2.5c. FID Truncation and Spectral Artifacts
2.5d. Resolution
2.6. Determination of NMR Spectra:  Spectral Presentation
2.6a. Signal Phasing and Baseline Correction
2.6b. Zero Referencing
2.6c. Determination of Certain NMR Parameters
2.7. Calibrations
2.7a. Pulse Width (Flip Angle)
2.8b. Decoupler Field Strength
Problems
Bibliography
3. The Chemical Shift
3.1. Factors That Influence Proton Shifts
3.2. Proton Chemical Shifts and Structure
3.2a. Saturated Aliphatics
3.2b. Unsaturated Aliphatics
3.2c. Aromatics
3.2d. Protons on Oxygen and Nitrogen
3.2e. Programs for Empirical Calculations
3.3. Medium and Isotope Effects
3.4. Factors That Influence Carbon Shifts
3.5. Carbon Chemical Shifts and Structure
3.5a. Saturated Aliphatics
3.5b. Unsaturated Compounds
3.5c. Carbonyl Groups
3.5d. Programs for Empirical Calculation
3.6. Tables of Chemical Shifts
Problems
Further Tips on Solving NMR Problems
Bibliography
4. The Coupling Constant
4.1. First- and Second-Order Effects
4.2. Chemical and Magnetic Equivalence
4.3. Signs and Mechanisms of Coupling
4.4. Couplings over One Bond
4.5. Geminal Couplings
4.6. Vicinal Couplings
4.7. Long-Range Couplings
4.8. Spectral Analysis
4.9. Tables of Coupling Constants
Problems
Bibliography
5. Further Topics in One-Dimensional NMR Spectroscopy
5.1. Spin-Lattice and Spin-Spin Relaxation
5.2. Reactions on the NMR Time Scale
5.3. Multiple Resonance
5.4. The Nuclear Overhauser Effect
5.5. Spectral Editing
5.6. Sensitivity Enhancement
5.7. Carbon Connectivity
5.8. Phase Cycling, Composite Pulses, and Shaped Pulses
Problems
Bibliography
6. Two-Dimensional NMR Spectroscopy
6.1. Proton-Proton Correlation Through J Coupling
6.2. Proton-Heteronucleus Correlation
6.3. Proton-Proton Correlation Through Space or Chemical Exchange
6.4. Carbon-Carbon Correlation
6.5. Higher Dimensions
6.6. Pulsed Field Gradients
6.7. Diffusion-Ordered Spectroscopy
6.7. Summary of Two-Dimensional Methods
Problems
Bibliography
7. Advanced Experimental Methods
Part A. One-Dimensional Techniques
7.1. T1 Measurements
7.2. 13C Spectral Editing Experiments
7.2a. The APT Experiment
7.2b. The DEPT Experiment
7.3. NOE Experiments
7.3a. The NOE Difference Experiment
7.3b. The Double-Pulse, Field-Gradient, Spin-Echo NOE Experiment
Part B. Two-Dimensional Techniques
7.4. Two-Dimensional NMR Data-Acquisition Parameters
7.4a. Number of Data Points
7.4b. Number of Time Increments
7.4c. Spectral Widths
7.4d. Acquisition Time
7.4e. Transmitter Offset
7.4f. Flip Angle
7.4g. Relaxation Delay
7.4h. Receiver Gain
7.4i. Number of Scans per Time Increment
7.4j. Steady-State Scans
7.5. Two-Dimensional NMR Data-Processing Parameters
7.5a. Weighting Functions
7.5b. Zero Filling
7.5c. Digital Resolution
7.5d. Linear Prediction
7.6. Two-Dimensional NMR Data Display
7.6a. Phasing and Zero Referencing
7.6b. Symmetrization
7.6c. Use of Cross Sections in Analysis
Part C. Two-Dimensional Techniques:  The Experiments
7.7. Homonuclear Chemical-Shift Correlation Experiments via Scalar Coupling
7.7a. The COSY Family:  COSY-90°, COSY-45°, Long-Range COSY, and DQF-COSY
7.7b. The TOCSY Experiment
7.8. Direct Heteronuclear Chemical-Shift Correlation via Scalar Coupling
7.8a. The HMQC Experiment
7.8b. The HSQC Experiment
7.8c. The HETCOR Experiment
7.9. Indirect Heteronuclear Chemical-Shift Correlation via Scalar Coupling
7.9a. The HMBC Experiment
7.9b. The FLOCK Experiment
7.9c. The HSQC-TOCSY Experiment
7.10. Homonuclear Chemical-Shift Correlation via Dipolar Coupling
7.10a. The NOESY Experiment
7.10b. The ROESY Experiment
7.11. 1D and Advanced 2D Experiments
7.11a. The 1D TOCSY Experiment
7.11b. The 1D NOESY and ROESY Experiments
7.11c. The Multiplicity-Edited HSQC Experiment
7.11d. The H2BC Experiment
7.11e. Nonuniform Sampling
7.11f. Pure Shift NMR
7.11g. Covariance NMR
7.12. Pure Shift-Covariance NMR
Bibliography
8. Structural Elucidation:  An Example
Part A. Spectral Analysis
8.1. 1H NMR Data
8.2. 13C NMR Data
8.3. The DEPT Experiment
8.4. The HSQC Experiment
8.5. The COSY Experiment
8.6. The HMBC Experiment
8.7. General Molecular Assembly Strategy
8.8. A Specific Molecular Assembly Procedure
8.9. The NOESY Experiment
Part B Computer-Assisted Structure Elucidation
8.10. CASE Procedures
8.11. T-2 Toxin
Appendix 1 Derivation of the NMR Equation
Appendix 2 The Bloch Equations
Appendix 3 Quantum Mechanical Treatment of the Two-Spin System
Appendix 4 Analysis of Second-Order, Three- and Four-Spin Systems by Inspection
Appendix 5 Relaxation
Appendix 6 Product-Operator Formalism and Coherence-Level Diagrams
Bibliography
Appendix 7 Stereochemical Considerations
A7.1. Homotopic Groups
A7.2. Enantiotopic Groups
A7.3. Diastereotopic Groups
Bibliography
Index