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The angular dependence of the muon Knight shift,K μ, and the muon relaxation rate in Bi at 11 K were measured in external magnetic fields up to 1 T. BothK μ and the second moment,M 2, are field dependent and involveP 4 0(cos θ) andP 4 3(cos θ) terms in the angular dependence. The Knight shift behaviour is discussed in terms of the dipole-dipole interaction and the de Haas-van Alphen effect, a consistent interpretation was not achieved in either case. The field dependence ofM 2 is in complete contrast to the second moment calculations and points to a field dependent redistribution of the charge distribution around the interstitial site.  相似文献   
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μ+ SR-measurements in transversally applied magnetic fields of 2000 G and 4000 G on heavy-electron single crystal U2Zn17 are presented. They reveal that at least two types of interstitial sites are occupied by the positive muons. One of these sites (1/3, 2/3, 5/6) could be identified via induced local dipolar fields which aboveT N=9.7 K can exactly be derived from the magnetic susceptibility. The corresponding component of the μ+-signal exhibits a steplike decrease by about 40% atT N which is caused by the onset of a very broad distribution of static internal magnetic fields (ΔB≈1000 G) with zero average. Such a field distribution is in distinct contrast to dipolar-field calculations performed for the simple antiferromagnetic structure deduced from neutron diffraction. The remaining 60% of the muons contributing to this component belowT N are subject to a narrow static field distribution (ΔB≈1 G). The induced dipolar fields at the site (1/3, 2/3, 5/6) are temperature-independent belowT N. A weak dipolar coupling to the U-moments renders similar observations for muons occupying the second type of interstitial impossible.  相似文献   
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Using a high purity Bi single crystal the temperature and orientation dependence of the zero and transverse field muon spin relaxation rate has been studied in detail. The results imply that the + occupies one of the two possible interstitial sites in the distorted rhombohedral crystal structure of Bi below 10 K and the other site above 80 K. At both sites the nearest neighbor Bi atoms are found to be shifted towards the + by 10% of their nominal distance, implying a large local lattice contraction. In concomitance extremely strong electric field gradients are manifest at the nn Bi nuclei. An almost temperature independent reduced relaxation rate in the temperature range from 20 K to 60 K is interpreted in terms of short range diffusion along a limited chain of alternating types of sites. Above 100 K both long range and short range diffusion are indicated.  相似文献   
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In single crystal samples of Zn, Cd and Be (hcp structure) stroboscopicSR measurements successfully revealed anisotropies in the muon Knight shift (K). An anisotropic K can provide information on the amount of non s-electrons screening the charge of the muon implanted in these metals as a light hydrogen isotope. In Cd, the anisotropic part depends strongly on the temperature and shows a change in sign at roughly 110 K. In Zn, the anisotropic part below 10 K turns out to comprise 4th order contributions in the direction cosines of the external field. This can be understood on the basis of an anisotropicg-factor of the conduction electrons or spin-orbit coupling, respectively.  相似文献   
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Racemic K-region imines of benz[a]anthracene, 7-methylbenz[a]anthracene, chrysene and benzo[a]pyrene ( 1–4 , respectively) have been resolved by high performance liquid chromatography on a column packed with amylose tris(3,5-dimethylphenylcarbamate) on silica gel. The absolute configuration of the resolved aziridines was assigned by comparison of their circular dichromism spectra to those of the corresponding enantiomerically pure arene oxides. The mutagenicity of the enantiomers of the arene imines was investigated using Salmonella typhimurium strains TA98 and TA100. Although all arene imines investigated were potent mutagens, quantitative and qualitative differences in the mutagenic activity were observed between enantiomers.  相似文献   
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Studies of Organometallic Compounds. XVII: Synthesis and Caracterisation of μ-oxo-bis(dicyclopentadienylmethyltitane IV) (Cp2TiCH3)2O is obtained by reacting (Cp2TiCl)2O with methyllithium. IR., NMR. and MS. spectrum are reported. Autocatalytic decomposition of the product is inferred from differential thermal analytic measurements.  相似文献   
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