Authors | |
Publisher | Springer Nature Switzerland AG |
Year | 23/02/2022 |
Pages | 313 |
Version | hardback |
Readership level | Professional and scholarly |
Language | English |
ISBN | 9783030887681 |
Categories | Quantum physics (quantum mechanics & quantum field theory) |
A Graduate Course in NMR Spectroscopy
Chapter-1: BASIC CONCEPTS
1.1 Nuclear Spin and Magnetic Moments
1.2 Nuclear Spins in a Magnetic Field
1.3 Spin Lattice Relaxation
1.4 Spin temperature1.5 Resonance Absorption of Energy and The NMR Experiment
1.5.1. The basic NMR spectrometer
1.6 Kinetics of Resonance Absorption
1.7 Selection Rules
1.8 Line widths
1.9 Bloch equations
1.10 More about relaxation
1.11 SensitivityEXERCISES
CHAPTER 2: HIGH RESOLUTION NMR SPECTRA OF MOLECULES
2.1 Introduction
2.2 Chemical Shift
2.2.1 Anisotropy of chemical shifts
2.2.2 Factors Influencing Isotropic Chemical shifts
2.3 Spin-Spin Coupling
2.4 Analysis of NMR spectra of molecules
2.4.1 First Order Analysis
2.4.2 Quantum Mechanical Analysis2.5 Dynamic Effects in the NMR spectra
2.5.1 Two site Chemical Exchange
2.5.2. Collapse of spin multiplets
2.5.3 Conformational Averaging of J- values
EXERCISES
CHAPTER 3: FOURIER TRANSFORM NMR
3.1 Introduction
3.2 Principles of Fourier transform NMR
3.3 Theorems on Fourier transforms
3.4 The FTNMR Spectrometer3.5. Practical aspects of recording FTNMR spectra
3.5.1. Carrier Frequency and off-set
3.5.2. RF pulse3.5.3. Free Induction Decay (FID) and the spectrum
3.5.4. Single channel and quadrature detection
3.5.5. Signal digitization and sampling3.5.6. Folding of signals
3.5.7. Acquisition time and the resolution
3.5.8. Signal averaging and Pulse repetition rate3.6. Data processing in FT NMR
3.6.1. Zero filling
3.6.2. Digital filtration or window multiplication or apodization3.7 Phase correction
3.8. Dynamic range in FTNMR
3.9. Spin-echo3.10. Measurement of relaxation times
3.10.1. Measurement of relaxation time
3.10.2. Measurement of relaxation time3.11. Water suppression through spin-echo: Watergate
3.12 Spin decoupling
3.13 Broad band decoupling
3.14 Biliniear Rotational Decoupling (BIRD)EXERCISES
CHAPTER 4: POLARIZATION TRANSFER
4.1 Introduction
4.2 Experimental Schemes
4.3 Origin of NOE
4.3.1 A simplified treatment
4.3.2 A more rigorous treatment4.4 Steady state NOE
4.5 Transient NOE
4.6. Selective population inversion
4.7. INEPT
4.7.1. Disadvantages of INEPT
4.8 Refocused INEPT
4.9 DEPT
EXERCISES
CHAPTER 5: Density matrix description of NMR
5.1 Introduction
5.2 Density matrix5.3 Elements of Density Matrix
5.4. Time evolution of density operator
5.5. Matrix representations of RF pulses
5.6. Product Operator Formalism
5.6.1. Basis operator sets
5.6.2. Time-evolution of Cartesian Basis Operators
5.6.2.1 Free evolution under the influence of the Hamiltonian5.6.2.2 Chemical Shift evolution
5.6.2.3 Scalar coupling evolution
5.6.2.4 Rotation by pulses5.6.2.5 Calculation of the spectrum of J-coupled two spin system
EXERCISES
Chapter 6: Multidimensional NMR Spectroscopy
6.1 Segmentation of the time axis
6.2 Two dimensional NMR6.3 Two-dimensional Fourier Transformation in NMR
6.4 Peak shapes in 2D spectrum
6.5 Quadrature detection in two-dimensional NMR6.6 Types of 2D-NMR spectra
6.6.1 2D- resolution/ separation experiments
6.6.2. Two-dimensional correlation experiments
6.6.2.1 The COSY experiment
6.6.2.1.1 COSY of two-spins
6.6.2.1.2 COSY of three-spins
6.6.2.1.3 Disadvantages of COSY
6.6.2.2 Double-Quantum Filtered COSY (DQF-COSY)
6.6.2.3 Total Correlation Spectroscopy (TOCSY)
6.6.2.4 Two-dimensional Nuclear Overhauser Effect spectroscopy (2D-NOESY)
6.6.2.5 Two-dimensional ROESY
6.6.3 Two-dimensional heteronuclear correlation experiments
6.6.3.1 Heteronuclear COSY
6.6.3.2 Heteronuclear Multiple Bond Correlation (HMBC)
6.6.3.3 Combination of mixing sequences
6.7 Three dimensional NMR
6.7.1 The CT-HNCA experiment
6.7.2 The HNN experiment6.7.3 The constant-time HN(CO)CA experiment
6.7.4 The HN(C)N experimentEXERCISES
APPENDIX
A1. Hamiltonian of dipole-dipole interactionA2. Chemical Shift Anisotropy
A3. Solid state NMR: basic features
A4. Coherence selection by linear Field Gradients
A5. Pure shift NMR: ZS and PSYCHE methods
A6. HADAMARD NMR for selective excitation