Carbon-13 nuclear magnetic resonance chemical shifts

Park, K.D., Guo, K., Adebodun, F., Chiu, M.L., Sligar, S.G., et al. Distal and proximal ligand interactions in heme proteins correlations between C-O and Fe-C vibrational liequencies, oxygen-17 and carbon-13 nuclear magnetic resonance chemical shifts, and oxygen-17 nuclear quadrupole coupling constants in C O- and CO-labeled species. Biochemistry 30, 2333-2347 (1991)... 

Over 100 SbCls affinity values are collected in Table 2.2. The sample of Lewis bases contains mainly oxygen bases and, among these, mainly carbonyl compounds. Only nine nitrogen bases (seven nitriles, one pyridine, one amine) have been studied. The scale lacks second-row bases, carbon bases and halogen bases. We have not reported the values estimated indirectly from correlations between DN and solvent basicity-dependent properties, such as nuclear magnetic resonance chemical shifts of the Na nucleus [27] or of the chloroform proton [28], These values would be valid only if there was no separation into families of bases in the correlation chart, which is rarely found. As shown in this book, family-dependent correlations between basicity-dependent properties are generally the norm. 

Csaszar, A. G. 1992. Conformers of Gaseous Glycine, J. Am. Chem. Soc. 114,9568-9575. de Dios, A. C., J. G. Pearson, and E. Oldfield. 1993. Chemical Shifts in Proteins An Ab Initio Study of Carbon-13 Nuclear Magnetic Resonance Chemical Shielding in Glycine, Alanine, and Valine Residues, J. Am. Chem. Soc. 115, 9768-9773. 

The carbon-13 nuclear magnetic resonance (cmr) shift spectra are given in the form of numbers adjacent to the carbons in the chemical structures. 

Inasmuch as establishing the carbon framework of a molecule overcomes a major obstacle to structure determination, carbon nuclear magnetic resonance ( C-NMR) spectroscopy is potentially the most powerful spectroscopic implement for natural products characterization. The broad range of chemical shifts are valuable in determining the presence of different functional groups (49, 84, 85, 235, 321,... 

The section on Spectroscopy has been retained but with some revisions and expansion. The section includes ultraviolet-visible spectroscopy, fluorescence, infrared and Raman spectroscopy, and X-ray spectrometry. Detection limits are listed for the elements when using flame emission, flame atomic absorption, electrothermal atomic absorption, argon induction coupled plasma, and flame atomic fluorescence. Nuclear magnetic resonance embraces tables for the nuclear properties of the elements, proton chemical shifts and coupling constants, and similar material for carbon-13, boron-11, nitrogen-15, fluorine-19, silicon-19, and phosphoms-31. 

Fig. 22. Carbon-13 nuclear magnetic resonance of carbonyl carbon chemical shifts on complexation of K.+.

If one wishes to obtain a fluorine NMR spectrum, one must of course first have access to a spectrometer with a probe that will allow observation of fluorine nuclei. Fortunately, most modern high field NMR spectrometers that are available in industrial and academic research laboratories today have this capability. Probably the most common NMR spectrometers in use today for taking routine NMR spectra are 300 MHz instruments, which measure proton spectra at 300 MHz, carbon spectra at 75.5 MHz and fluorine spectra at 282 MHz. Before obtaining and attempting to interpret fluorine NMR spectra, it would be advisable to become familiar with some of the fundamental concepts related to fluorine chemical shifts and spin-spin coupling constants that are presented in this book. There is also a very nice introduction to fluorine NMR by W. S. and M. L. Brey in the Encyclopedia of Nuclear Magnetic Resonance.1... 

The fourth chapter in this volume, contributed by Helmut Duddeck, is an exceptionally thorough survey of substituent effects on carbon-13 nuclear magnetic resonance (NMR) chemical shifts. Organic chemists and others who are routinely dependent on 13C NMR for structure elucidation and for information about stereochemistry will welcome the summary presented here. Although... 

The H and nuclear magnetic resonance (NMR) chemical shift of all the parent structures are fully reported in CHEC-II(1996) <1996CHEC-II(6)447>. Since then, the complete proton and carbon chemical shift assignments have been made for 2- and 3-formyl, acetyl, or methyl phenoxathiin <1996PJC36>. 

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