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Nuclear magnetic resonance nuclei possibility

Wachtell (Ref 23) worked on the application of this principle. However, early in his work a major problem was encountered in finding the quadrupole resonance of the chlorine nucleus which did not exist in the frequency range in which it had been expected (20—40 megacycles). Nuclear Magnetic Resonance studies finally have shown that this quadrupole resonance should exist around 150 kilocycles. Future studies of single crystals of AP should reveal the presence and the exact location of this resonance. If this can be done, then the analysis of particle size, based on the shift of the quadrupole resonance frequency, may be possible... [Pg.535]

Figure 9-21 Schematic representation of the possible alignments of a magnetic nucleus (here hydrogen) in an applied magnetic field. Transitions between the two states constitute the phenomenon of nuclear magnetic resonance. The arrows through the nuclei represent the average component of their nuclear magnetic moment in the field direction. Figure 9-21 Schematic representation of the possible alignments of a magnetic nucleus (here hydrogen) in an applied magnetic field. Transitions between the two states constitute the phenomenon of nuclear magnetic resonance. The arrows through the nuclei represent the average component of their nuclear magnetic moment in the field direction.
NMR refers to nuclear magnetic resonance spectroscopy. The nucleus most commonly studied with nmr is the hydrogen nucleus, but it is possible to study the nucleus of carbon-13 and other atoms as well. [Pg.89]

The enormous advances and changes in organometallic chemistry since the discovery of ferrocene would not have been possible had there not been a concomitant development of instrumental techniques and widespread availability of instruments. Infrared spectroscopy has long been known, but recent extensions in both theory and instrumentation have greatly expanded its applications. More recently, it has been complemented and supplemented by Raman spectroscopy. Nuclear magnetic resonance (NMR) spectroscopy, particularly for the hydrogen nucleus, has been an extremely important tool much early work is reviewed in the article by Maddox et al. 172). In more recent years, nuclei such as F, °B, and a variety of others have also... [Pg.27]

The structure and identity of such compounds that are of practical relevance as com-plexing agents may be elucidated unequivocally by both one-dimensional and two-dimensional nuclear magnetic resonance spectroscopy of the isotopes H-l, C-13, and P-31. Sufficiently high concentrations also render possible their quantitative analysis [87-91]. However, because of the low sensitivity, especially of the phosphorus nucleus, problems are encountered with the limits of detection in practical applications. [Pg.132]

The foundation of MRI is a phenomenon called nuclear magnetic resonance (NMR), which was discovered in the mid-1940s. Today NMR has become one of the most important spectroscopic methods used in chemistry. NMR is based on the observation that, like electrons, the nuclei of many elements possess an intrinsic spin. Like electron spin, nuclear spin is quantized. For example, the nucleus of H has two possible magnetic nuclear spin quantum numbers, -I-j and - y... [Pg.236]

Nuclear magnetic resonance (NMR) in principle gives information about the environment of a nucleus that possesses a magnetic dipole. For solid samples, which of course include all LDH derivatives, special techniques must be employed to average out the effects of local anisotropies, and even so it is not possible to obtain the superb resolution typical of solution NMR spectra (301). Despite these limitations, the technique has been extensively applied to LDH derivatives, with H (287,329,330), (287), N (331), Cl (332), Se (333), Al... [Pg.413]


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