15N-NMR Spectroscopy
Published on 1. April 1981
Book
Hardback
VII, 384 pages
978-3-540-10459-9 (ISBN)
Description
After the proton and carbon, nitrogen is, with oxygen, the most impor tant atom in organic and especially bioorganic molecules. However, the development of nitrogen spectroscopy is indeed very recent. This is due to the fact that nitrogen-14, which is the naturally abundant iso tope, suffers, for structural studies, from the disadvantages inherent in nuclei with a quadrupolar moment (Table 1.1). Actually, indirect 15N measurements were reported in the early days of double resonance spectroscopy and the first direct detection of 15N resonance signals at the natural abundance level was realized in 1964 (R 17) at 4.33 MHz 1 (~ 1T) using a 15 mm o.d. cell in the field sweep mode (~ 0.16 min- ). Signal-to-noise ratios only of 3-4 were obtained for neat liquids and this low sensitivity of the 15N resonance still remains the main dis advantage for 15 spectroscopy (Table 1.1). However, nitrogen-15 has, N probably more than any other nucleus, benefited from the advances of NMR technology, i.e. Fourier transformation, multinuclear facilities, wide-bore super conducting solenoids, and, with the new generation of spectrometers, 15N-NMR is entering the field of routine investigation. Nevertheless, in spite of these spectacular improvements, obtaining 15N spectra of diluted species or large biochemical molecules is often not very easy and a good knowledge of the relaxation properties pecu liar to 15N may be necessary in order to adjust the pulse sequences and the decoupler duty cycle correctly (Section 2).
More details
Series
Language
English
Place of publication
Heidelberg
Germany
Publishing group
Springer Berlin
Target group
Professional and scholarly
Illustrations
10
10 s/w Abbildungen
10 black & white illustrations, biography
Weight
760 gr
ISBN-13
978-3-540-10459-9 (9783540104599)
DOI
10.1007/978-3-642-50172-2
Schweitzer Classification
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G.J. Martin | M.L. Martin | J.-P. Gouesnard
15N-NMR Spectroscopy
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12/2012
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15N-NMR Spectroscopy
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Content
1 Introduction.- Table.- 2 Relaxation Phenomena and Nuclear Overhauser Effects. Molecular Dynamics and Observation of the 15N Signals.- 2.1 The Mechanisms of Nitrogen Relaxation.- 2.2 Electron Nuclear Relaxation and Influence of Paramagnetic Species.- 2.2.1 Effect of Paramagnetic Impurities.- 2.2.2 Use of Relaxation Reagents.- 2.3 Nitrogen Relaxation in Small Molecules.- 2.4 Nitrogen Relaxation in Large Molecules. The Isotopic Substitution Method.- 2.5 The Nuclear Overhauser Effect.- Tables.- 3 Experimental Techniques in 15N Spectroscopy.- 3.1 Experimental Methods for Recording 15N Spectra.- 3.1.1 Indirect Detection: CW INDOR Spectra and FT Double Resonance Experiments.- 3.1.2 The Conventional Single Pulse Method.- 3.1.3 Methods of Polarization Transfer.- 3.2 Sample Preparation.- 3.2.1 The NMR Cell.- 3.2.2 Purification of the Sample.- 3.2.3 Chemically Assisted 15N Spectroscopy.- 3.2.4 15N Labelling Experiments.- Tables.- 4 Reference for 15N Chemical Shifts.- 4.1 External and Internal Locking and Referencing.- 4.2 The Various References Used in 15N Spectroscopy. Conversion to the External Nitromethane Scale.- 4.3 Universal Scales of Nitrogen Chemical Shifts.- 4.4 Absolute Nitrogen Shieldings.- Tables.- 5 Medium Effects in 15N Spectroscopy.- 5.1 Physical Properties and Polarity Factors of Solvents.- 5.1.1 Physical Properties of Solvents.- 5.1.2 Empirical Parameters of Solvent Polarity.- 5.2 Solvent Effects on 15N Chemical Shifts.- 5.2.1 Qualitative Discussion of Solvent-Induced 15N Shifts.- 5.2.2 Quantitative Treatment of Solvent-Induced 15N Shifts.- 5.3 Solvent Effects on nJ15N~X Coupling Constants.- 5.3.1 Direct Solvent Effects on nJ15N~X Coupling Constants.- 5.3.2 Protonation Effects on nJ15N~X Coupling Constants.- 5.3.3 Indirect Solvent Effects on nJN~X Coupling Constants (Tautomeric Equilibria).- Table.- 6 15N Chemical Shifts.- 6.1 Tables of 15N Chemical Shifts.- 6.1.1 Accuracy of 15N Chemical Shift Determination.- 6.1.2 List of Tables of ?15N Data.- 6.1.3 Bioorganic Molecules.- 6.2 Correlation Analysis of 15N Chemical Shifts.- 6.2.1 Correlation between ?15N and Topological Qualitative Parameters.- 6.2.2 Correlations between ?15N and Chemical Shifts of Other Nuclei.- 6.2.3 Correlations between and Computed Electronic Density Q.- 6.2.4 Correlation between ?15N and Hammett-like Substituent Parameters.- 6.2.5 Correlations between ?15N and Free Energies of Activation of Hindered Rotation Processes about N-X Bonds.- 6.2.6 Correlations between ?15N and Various Parameters (?, IP, dN-N'?IR', pH).- Tables.- 7. nJ15N~X Coupling Constants.- 7.1 Tables of nJ15N~X Coupling Constants.- 7.2 Correlation Analysis of nJ15N~X Coupling Constants.- 7.2.1 nJ15N~X Coupling Constants.- 7.2.2 Coupling Constants.- 7.2.3 Coupling Constants between 15N and Other Hetero Nuclei.- Tables.- 8 Application of 15N Spectroscopy to the Study of Dynamic Processes and Reaction Mechanisms.- 8.1 Exchange Processes studied by Line-Shape Modification Experiments.- 8.1.1 Practical Aspects of Dynamic NMR of Rare Isotopes.- 8.1.2 Line-Shape Modifications Due to Modulation of Scalar Coupling Interactions by Proton Transfers.- 8.1.3 Line-Shape Modifications Involving Chemical Shift Averaging.- 8.2 CIDNP Experiments.- 8.3 Application of 15N Spectroscopy to the Study of Chemical and Biochemical Mechanisms.- 8.3.1 Tautomerism in Nitrogen Derivatives.- 8.3.2 Application of 15N Spectroscopy to the Study of Chemical Mechanisms.- 8.3.3 Applications of 15N Spectroscopy to the Study of Biochemical Mechanisms.- References.- Index of Compounds.