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The properties of two-dimensional four-pulse electron spin echo envelope modulation spectra of nuclei with nuclear spin I = 3/2 in disordered systems are discussed by means of calculated lithium hyperfine sublevel correlation spectra. Since a case of small coupling is treated, the multifrequency transition components appear only in the first quadrant of the two-dimensional spectra. The influence of the hyperfine and nuclear quadrupole interaction parameters on the cross peak ridges in the two-dimensional powder pattem is analyzed. Furthermore the possibility to determine the magnitude of the dipolar hyperfine and the nuclear quadrupole coupling from the cross peak line shapes is investigated. In this context the potential of those spectral features representing the so-called multiquantum transitions for the interpretation of the spectra is demonstrated.

Di-tert-butyl nitroxide was adsorbed on LiY zeolites, and the formation of adsorption complexes of this radical with lithium cations was proven by means of two-dimensional electron spin−echo modulation spectroscopy. The evaluation of the experimental hyperfine sublevel correlation spectra revealed a negative isotropic hyperfine coupling for both lithium isotopes. Furthermore a complex geometry was obtained where the Li + ion is located within the molecular mirror plane of the DTBN nitroxide radical with an oxygen−lithium cation bond length of 0.19 nm.

The location and coordination geometry of vanadium(IV) ions in the cesium salt of molybdovanadophosphoric heteropolyacid Cs(4)PVMo(11)O(40) were studied using orientation-selective pulsed ENDOR (electron nuclear double resonance) experiments. To enhance the orientation selectivity for the paramagnetic vanadyl species, these investigations were done at Q-band frequencies. It was possible to resolve interactions of the paramagnetic vanadyl ions (VO(2+)) with all relevant nuclei, (1)H, (31)P, (51)V, and (133)Cs. The location of the vanadyl species was studied by determination of the complete (31)P hyperfine tensor. This approach was done for both the fresh and the calcined Cs(4)PVMo(11)O(40) materials, and no differences in the structures of the VO(2+) complexes were found. The ENDOR results give experimental evidence for the location of the V(IV) ions. For both samples, it was possible to exclude the incorporation of V(IV) at the Mo sites. The VO(2+) species are directly attached to the outer surface of the heteropolyanion and coordinated to four of the outer oxygen atoms with a V-P distance of 3.96 A.