Nuclear Magnetic Resonance of OrientedAu196,Au198, andAu200m

Abstract
Thermal equilibrium nuclear orientation was employed to orient nuclei of Au196, Au198, and Au200m as dilute impurities in nickel and iron at temperatures down to 4 mK. The degree of nuclear orientation was determined from the anistropy of γ radiation emitted from the oriented nuclei. For Ni(Au200m) both the magnetic hyperfine interaction |μH|=(7.65±0.30)×1018 erg and the magnetic hyperfine splitting |μHI|=(6.473±0.012)×1019 erg were determined from an analysis of the temperature dependence of γ-ray anisotropies and by nuclear magnetic resonance on oriented nuclei (NMR/ON), respectively. As a result the spin I and the magnetic moment μ of the isomeric state could be derived as Iπ=12() and μ(12)={+}{()}(6.10±0.20)μN. From the measured anisotropies of five γ rays originating from the β decay of Au200m, spins and multipolarities could be assigned in the Hg200 decay scheme. Nuclear magnetic resonance was also observed on oriented Au196 and Au198 in nickel at frequencies of 58.3±0.4 MHz and 58.5±0.4 MHz, respectively. The hyperfine interaction for Ni(Au197), measured previously by spin echo, and our result for Ni(Au196,198) agree with the known atomic hyperfine anomalies between Au197 and Au196,198 only if the hyperfine field is assumed to have a noncontact contribution. For Ni(Au196,198) with Hhf=()260.8±1.3 kOe, the contact part is then found to be Hc=367±70 kOe, with the noncontact contribution amounting to Hnc=+106±70 kOe. The angular distributions of several γ rays are in excellent agreement with a decay scheme proposed by Cunnane et al., in which they found negative-parity levels of spins 5, 7, 9, and 11 at energies of 1852, 1963, 2144, and 2642 keV, respectively, in Hg200.