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Resonance condition electronic Zeeman interaction

Now we can define the anisotropic resonance condition for an S = 1/2 system subject to the electronic Zeeman interaction only as... [Pg.74]

For nitroxides in dilute liquid solution, the generally anisotropic spin Hamilton operator is simplified tremendously and, if imresolved proton hyperfine couplings are treated as line broadening, only the electron-Zeeman interaction and the hyperfine coupling to the magnetic nucleus (7 = 1) remain [20]. The g- and hyperfine (4-) tensors are averaged to isotropic values due to fast motion of the spin probe and the resonance condition for the irradiated microwave becomes... [Pg.74]

Before we develop the resonance conditions for systems with hyperhne and with zero-held interactions, we return to the electronic Zeeman term S B as an example interaction to discuss a hitherto ignored complexity that is key to the usefulness of EPR spectroscopy in (bio)chemistry, namely anisotropy the fact that all interactions... [Pg.70]

One key aspect of ENDOR spectroscopy is the nuclear relaxation time, which is generally governed by the dipolar coupling between nucleus and electron. Another key aspect is the ENDOR enhancement factor, as discussed by Geschwind [294]. The radiofrequency frequency field as experienced by the nucleus is enhanced by the ratio of the nuclear hyperfine field to the nuclear Zeeman interaction. Still another point is the selection of orientation concept introduced by Rist and Hyde [276]. In ENDOR of unordered solids, the ESR resonance condition selects molecules in a particular orientation, leading to single crystal type ENDOR. Triple resonance is also possible, irradiating simultaneously two nuclear transitions, as shown by Mobius et al. [295]. [Pg.138]


See other pages where Resonance condition electronic Zeeman interaction is mentioned: [Pg.147]    [Pg.222]    [Pg.51]    [Pg.84]    [Pg.457]    [Pg.82]    [Pg.119]   
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