Abstract
The range of 13C chemical shifts is normally 0-230 ppm. In a proton- decoupled spectrum they are found as sharply resolved single peaks, and they are measured with reference to TMS taken as zero, although addition of TMS is often not carried out since the position of the solvent signal with reference to TMS is known, and the signals may be calibrated with reference to the solvent signal. The chemical shifts of common solvents are presented in Table 4.1.
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J.W. Cooper, Spectroscopic Techniques for Organic Chemists, John Wiley and Sons, New York (1980).
D. Shaw, Pulsed Fourier Transform NMR Spectroscopy, Elsevier Scientific Publishing Co., Amsterdam (1979).
F.W. Wehrli and T. Wirthlin, Interpretation of Carbon-13 NMR Spectra, Heyden and Son Ltd., London (1978).
G.C.Levy, Ed., Topics in Carbon-13 NMR Spectroscopy, Vols. 1-3, John Wiley and Sons, New York (1979).
E. Breitmaier and W. Voelter,13C-NMR Spectroscopy, Verlag Chemie,Weinheim (1978)
C. Brevard and P. Graner, Handbook of High Resolution Multinuclear NMR, John Wiley and Sons, New York (1981).
G.C. Levy, R.L. Lichter, and G.L. Nelson, Carbon-13 Nuclear Magnetic Resonance Spectroscopy, John Wiley and Sons, New York (1980).
H. Günther, NMR Spectroscopy, John Wiley and Sons, New York (1980).
L.M. Jackman and S. Sternhell, Applications of Nuclear Magnetic Resonance Spectroscopy in Organic Chemistry, International Series in Organic Chemistry, Vol. 10, Pergamon Press, Oxford (1969).
F.A. Bovey, Nuclear Magnetic Resonance Spectroscopy, Academic Press, New York (1969).
E.D. Becker, High Resolution NMR, Academic Press, New York (1980).
M.L. Martin and G.J. Martin, Practical NMR Spectroscopy, Heyden and Son Ltd., London (1980).
T. Clerc and E. Pretsch, Kernresonanz Spektroskopie, Akademische Verlagsgesell-schaft, Frankfurt (1973).
A. Carrington and A.D. McLachlan, Introduction to Magnetic Resonance, Chapman and Hall, London (1979).
H. Saito, G.Izumi, T. Mamizuka, S.Suzuki, and T.R.Tabeta, A 13C cross polarisation-magic angle spinning (CP-MAS) NMR study of crystalline cyclohexa-amylose inclusion complexes. Conformation-dependent 13C chemical shifts are related to the dihedral angles of glycosidic linkages. J. Chem. Soc., Chem. Commun., 13–86(1982).
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© 1986 Springer-Verlag New York Inc.
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Atta-ur-Rahman (1986). Chemical Shifts and Spin—Spin Couplings in 13C-NMR Spectroscopy. In: Nuclear Magnetic Resonance. Springer, New York, NY. https://doi.org/10.1007/978-1-4612-4894-1_4
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DOI: https://doi.org/10.1007/978-1-4612-4894-1_4
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