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15N-NMR Spectroscopy (Paperback, Softcover reprint of the original 1st ed. 1981)
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15N-NMR Spectroscopy (Paperback, Softcover reprint of the original 1st ed. 1981)
Series: NMR Basic Principles and Progress, 18
Expected to ship within 10 - 15 working days
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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).
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