200 and More NMR Experiments

A Practical Course
2. expanded Auflage, Nachdrucked 2004
ISBN: 978-3-527-31067-8
Verlag: Wiley-VCH GmbH

Buch, Englisch, 838 Seiten, Format (B × H): 170 mm x 244 mm, Gewicht: 1635 g

This work-book will guide you safely, in step-by-step descriptions, through every detail of the NMR experiments within, beginning with 1D routine experiments and ending with a series of advanced 3D experiments on a protein:
 
· Which experiment can best yield the desired information?
· How must the chosen experiment be performed?
· How does one read the required information from the spectrum?
· How does this particular pulse sequence work?
· Which other experiments give similar information?
 
This third edition of the book, following its two highly successful predecessors, has been revised and expanded to 206 experiments. They are organized in 15 chapters, covering test procedures and routine spectra, variable temperature measurements, the use of auxiliary reagents, 1D multipulse experiments, spectra of heteronuclides, and the application of selective pulses. The second and third dimensions are introduced using pulsed field gradients, and experiments on solid state materials are described. A key part describes 3D experiments on the protein ubiquitin with 76 amino acids.
 
What is new in this third edition?
 
1. 24 new experiments have been inserted into the 14 chapters that were in the 2nd edition, e.g., alpha/beta-SELINCOR-TOCSY, WET, DOSY, ct-COSY, HMSC, HSQC with adiabatic pulses, HETLOC. J-resolved HMBC, (1,1)- and (1,n)-ADEQUATE, STD, REDOR, and HR-MAS.
2. 20 new protein NMR experiments have been specially devised and are collected in the newly added Chapter 15, ProteinNMR, for which one needs a special model sample: fully 13C- and 15N-labeled human ubiquitin. Techniques used include the constant time principle, the PEP method, filters, gradient selection, and the echo/anti-echo procedure.
 
The guide has been written by experts in this field, following the principle of learning by doing: all the experiments have been specially performed for this book, exactly as described and shown in the spectra that are reproduced. Being a reference source and work-book for the NMR laboratory as well as a textbook, it is a must for every scientist working with NMR, as well as for students preparing for their laboratory courses

Zielgruppe

Organiker, Physikochemiker, Analytiker, Studenten der Chemie

Autoren/Hrsg.

Berger, Stefan

Braun, Siegmar

Fachgebiete

• Naturwissenschaften Chemie Chemie Allgemein Chemometrik, Chemoinformatik
• Naturwissenschaften Chemie Chemie Allgemein Pharmazeutische Chemie, Medizinische Chemie
• Naturwissenschaften Chemie Chemie Allgemein Chemische Labormethoden, Stöchiometrie
• Naturwissenschaften Chemie Analytische Chemie Massenspektrometrie, Spektroskopie, Spektrochemie
• Naturwissenschaften Chemie Chemie Allgemein Toxikologie, Gefahrstoffe, Sicherheit in der Chemie

Inhaltsverzeichnis

Preface v

Chapter 1 The NMR Spectrometer 1

1.1 Components of an NMR Spectrometer 1

1.1.1 The Magnet 1

1.1.2 The Spectrometer Cabinet 2

1.1.3 The Computer 3

1.1.4 Maintenance 3

1.2 Tuning a Probe-Head 3

1.3 The Lock Channel 4

1.4 The Art of Shimming 6

1.4.1 The Shim Gradients 6

1.4.2 The Shimming Procedure 8

1.4.3 Gradient Shimming 11

Chapter 2 Determination of Pulse-Duration 14

Exp. 2.1: Determination of the 90° 1H Transmitter Pulse-Duration 15

Exp. 2.2: Determination of the 90° 13C Transmitter Pulse-Duration 18

Exp. 2.3: Determination of the 90° 1H Decoupler Pulse-Duration 21

Exp. 2.4: The 90° 1H Pulse with Inverse Spectrometer Configuration 24

Exp. 2.5: The 90° 13C Decoupler Pulse with Inverse Configuration 27

Exp. 2.6: Composite Pulses 30

Exp. 2.7: Radiation Damping 33

Exp. 2.8: Pulse and Receiver Phases 36

Exp. 2.9: Determination of Radiofrequency Power 39

Chapter 3 Routine NMR Spectroscopy and Standard Tests 43

Exp. 3.1: The Standard 1H NMR Experiment 44

Exp. 3.2: The Standard 13C NMR Experiment 49

Exp. 3.3: The Application of Window Functions 54

Exp. 3.4: Computer-Aided Spectral Analysis 58

Exp. 3.5: Line Shape Test for 1H NMR Spectroscopy 61

Exp. 3.6: Resolution Test for 1H NMR Spectroscopy 64

Exp. 3.7: Sensitivity Test for 1H NMR Spectroscopy 67

Exp. 3.8: Line Shape Test for 13C NMR Spectroscopy 70

Exp. 3.9: ASTM Sensitivity Test for 13C NMR Spectroscopy 73

Exp. 3.10: Sensitivity Test for 13C NMR Spectroscopy 76

Exp. 3.11: Quadrature Image Test 79

Exp. 3.12: Dynamic Range Test for Signal Amplitudes 82

Exp. 3.13: 13° Phase Stability Test 85

Exp. 3.14: Radiofrequency Field Homogeneity 88

Chapter 4 Decoupling Techniques 91

Exp. 4.1: Decoupler Calibration for Homonuclear Decoupling 92

Exp. 4.2: Decoupl

Über Autor(innen)

Stefan Berger was intrigued by NMR after having won a bottle of beer during an introductory course in organic NMR led by Professor H. Suhr at the University of Tübingen in 1968. After completing a PhD thesis with Professor Anton Rieker, in 1973 he joined Professor J. D. Roberts at Caltech for postdoctoral work, where he also met Professor D.M. Grant and Professor D. Seebach, who were then guest professors in Pasadena. This period was decisive to try a Habilitation in NMR spectroscopy, which was achieved at the University Marburg. At the University Leipzig his aim is to combine methodological development of NMR and its application to bioorganic problems.