Nuclear magnetic resonance spectroscopy zero-field

Zero-Field Nuclear Magnetic Resonance Spectroscopy. 

The pulse Fourier transform approach to magnetic resonance spectroscopy has been extensively developed and successfully applied to systems of one-half spin and their mutual interactions. But resonance spectroscopy of spin systems with the higher half- and integer spin quantum numbers is commonplace, for example, in the case of alkali metal nuclear magnetic resonance (NMR) and electron paramagnetic resonance (EPR) of transition metal compounds involving multi-quantum transitions. Similarly, magnetic resonance at zero field entails the observation of multi-quantum transitions. 

Liao. M.-Y. Harbison, G.S. Two-dimensional nuclear magnetic resonance correlation spectroscopy at zero field. J. Chem. Phys. 1999. 111. 3077-3082. 

The new techniques of phosphorescence-microwave multiplet resonance spectroscopy with optical detection have been reviewed by El-Sayed and Kwiram Such exciting experiments as the optical detection on electron-nuclear double resonance (ENDOR) and of electron-electron double resonance (EEDOR) in zero magnetic field have been achieved, and it is certain that much detailed knowledge concerning the phosphorescent states will evolve from this field. 

In this section we have described in considerable detail just one aspect of the spectroscopy of OH, namely, the measurement of zl-doubling frequencies and their nuclear hyperfine structure. This has led us to develop the theory of the fine and hyperfine levels in zero field as well as a brief discussion of the Stark effect. We should note at this point, however, that OH was the first transient gas phase free radical to be studied by pure microwave spectroscopy [121], We will describe these experiments in chapter 10. We note also that magnetic resonance investigations using microwave or far-infrared laser frequencies have also provided much of the most important and accurate information these studies are described in chapter 9, where we are also able to compare OH with the equally important radical, CH, a species which, until very recently, had not been detected and studied by either electric resonance techniques or pure microwave spectroscopy. 

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