μ + SR studies of UM2Al3, M=Ni,Pd

Positive-muon spin rotation ( ⁺ SR) measurements have been carried out in the new heavy-fermion superconductors UM₂Al₃, M=Ni and Pd. In UNi₂Al₃ the observed ⁺ frequencies in zero applied field indicate commensurate antiferromagnetic (AF) ordering of U moments 0.1 _B /U atom. These moments coexist with superconductivity and have the highest values observed in an AF heavy-fermion superconductor. The absence of well-defined frequencies in zero-field ⁺ SR in the AF state of UPd₂Al₃ suggests symmetric ⁺ stopping sites. In this system ⁺ SR linewidths belowT _c yield a preliminary value of 8000 Å for the London penetration depth.     

Muon knight shift in platinum and in β-PdHx (x=0.70, 0.75, 0.86)

The ⁺ Knight shift in Platinum has been measured between 20 K and 785 K. It shows a strong temperature dependence and scales with the magnetic bulk susceptibility. A temperature independent contribution of +53±15 ppm and a d-electron induced hyperfine field per unpaired d-electron per atom of B _hfd ^a =–5.03 kG(±8.5%) are obtained. The ⁺ Knight shift in PdH_0.70, PdH_0.75 and PdH_0.86 shows no dependence on temperature between 20 K and RT and increases from K=–(8±3) ppm for x=0.70 to K =+(6.5±3) ppm K=+(6.5±3) ppm for x=0.86, in good agreement with proton Knight shift measurements.     

Notiz über Methoden zur Umwandlung von 1,2-Dicarbonsäuren in konjugiert ungesättigte Monocarbonsäuren. Über synthetische Methoden, 12.Mitteilung

A Note on Methods for the Transformation of 1,2-Dicarboxylic Acids into α, β-Unsaturated Monocarboxylic Acids. A model study using the Diels-Alder adduct of maleic anhydride and butadiene (see scheme 3) exemplifies the conversion of the succinic acid type of structure into α, β-unsaturated carboxylic acids via two complementary fragmentations of 3,6-dioxo-perhydro-1,2-oxazine derivatives.     

Structures and Mutagenic Properties of Products Obtained by C-Nitrosation of Opipramol

Reaction of the tricyclic psychotropic drug opipramol ( 1 ) with an excess of HNO₂ affords a product mixture mutagenic for Salmonella typhimurium. The main product is a tetracyclic furoxan 2 (yield ca. 80%), resulting from nitrosation at C(10) and C(11) of 1 . Compound 2 is not mutagenic. The essential mutagen is a nitroarene 3 formed via contraction of the central ring of 1 , and nitrosation at C(2). Its yield is extremely low (<0.1%). Nitroarenes have previously not been encountered as mutagenic products of the interaction of drugs with nitrite.     

Possibility of a Lifshitz phase transition in Cd observed by a singularity in the muon Knight shift

During the past much effort has been devoted to a systematic study of the muon Knight shiftK in metallic environments and its implications on the local electronic structure of hydrogen in metals [1]. These measurements in simple metals were essentially all carried out in polycrystalline samples at room temperature. The present measurements in Cd in polycrystalline and single crystal samples cover a temperature range between 20 K and the melting point of this strongly anisotropic metal (hcp crystal structure,c/a ratio 1.89 — idealc/a ratio 1.63). These measurements add qualitatively new and interesting aspects and insights on the screening of a light hydrogen isotope in a metal as well as on certain properties of the host material itself. The outstanding features of the muon Knight shift in Cd are: (i) a strong intrinsic temperature dependence with an increase ofK of more than 100% between 20 K and the melting point (T=593 K), (ii) an anomaly at 110 K in the form of a singularity in the isotropic part ofK which is interpreted as a band structure effect, (iii) an anisotropic Knight shift contribution fitting the expressionK(T,)=K _iso(T)+K _ax(T) * (3 · cos² –1)/2, where both, the isotropic and the axial contribution ofK , are strongly temperature dependent.     

Substituenteneffekte auf die NMR-Spektren von Pentafulvenen. (13C, 13C)-NMR-Kopplungskonstanten (1J(C,C))

Substituent Effects on NMR Spectra of Pentafulvenes. ¹³C, ¹³C-NMR Coupling Constants (¹J(C, C)) ¹H- and ¹³C-NMR spectra of 6-monosubstituted pentafulvenes 1 – 8 have been analysed, and ¹J(C, C) coupling constants have been determined from ID-inadequate spectra of ¹³C satellites. It turns out that ¹³C,¹³C coupling constants of the ring C-atoms, and especially J(1,2)/J(3,4) and J(2,3), reflect the extent of π delocalisation in the fulvene ring. With increasing electron-donating capacity of the substituent R, J(1,2)/J(3,4) values are decreasing, while J(2,3) (and J(1,5)/J(4,5) as well) are increasing, and linear correlations of Hammett substituent constants σ⁺ and ¹J(C,C) values are obtained.