The ϱ−ππ coupling constant in lattice gauge theory

We present a method for studying hadronic transitions in lattice gauge theory which requires computer time comparable to that required by recent hadron spectrum calculations. This method is applied to a calculation of the decay ?→ππ.     

Sequential intermediates in the base-catalyzed conversion of bis(pi-conjugated propargyl) sulfones to 1,3-dihydrobenzo- and naphtho[c]thiophene-2,2-dioxides

[reaction: see text] In a recent article, we reported on the base-catalyzed rearrangements of dipropargyl selenides, -sulfides, -sulfoxides, and -sulfones that eventually lead to polycyclic aromatic products. In the present work, we report on the first isolation and characterization of the thiophene dioxide intermediates 5b,c from a mild tandem isomerization/cyclization/aromatization of bis(pi-conjugated propargyl) sulfones. Monoallene 2b,c and diallene 3b intermediates were also identified by NMR. A kinetic study of the rearrangement of 1a-c revealed that the unusual facile tandem process is highly dependent on the nature of gamma-substitution.     

Semileptonic decays of d mesons in three-flavor lattice QCD

We present the first three-flavor lattice QCD calculations for D-->pilnu and D-->Klnu semileptonic decays. Simulations are carried out using ensembles of unquenched gauge fields generated by the MILC Collaboration. With an improved staggered action for light quarks, we are able to simulate at light quark masses down to 1/8 of the strange mass. Consequently, the systematic error from the chiral extrapolation is much smaller than in previous calculations with Wilson-type light quarks. Our results for the form factors at q(2)=0 are f(D-->pi)(+)(0)=0.64(3)(6) and f(D-->K)(+)(0)=0.73(3)(7), where the first error is statistical and the second is systematic, added in quadrature. Combining our results with experimental branching ratios, we obtain the Cabibbo-Kobayashi-Maskawa matrix elements |V(cd)|=0.239(10)(24)(20) and |V(cs)|=0.969(39)(94)(24), where the last errors are from experimental uncertainties.     

Structure and soft mode behavior of two chalcogenide crystals

The crystal structures of T?₃PSe₄ and T?₃AsS₄ have been determined by x-ray diffraction techniques. These isomorphous materials are layered, with orthorhombic Pcmn symmetry. Ultrasonic measurements have shown that the $\text{a}$$\text{b}$ shear mode velocity is anomalously low for both materials. Measurements at high pressure on T?₃PSe₄ have shown that the anomalous shear velocity softens to zero at 1.40 ± 0.01 GPa, indicating a second- order structural transition at that pressure.     

On The Navier-Stokes Equations with Constant Total Temperature

For various applications in fluid dynamics, one can assume that the total temperature is constant. Therefore, the energy equations can be replaced by an algebraic relation. The resulting set of equations in the inviscid case is analyzed in this paper. It is shown that the system is strictly hyperbolic and well posed for the initial-value problem. Boundary conditions are described such that the linearized system is well posed. The hopscotch method is investigated and numerical results are presented.     

Stabilization of a multi-tethered lighter-than-air rigid-body sphere undergoing vortex-induced vibrations in uniform flow

Nonlinear Dynamics - We consider the stabilization of a multi-tethered lighter-than-air sphere undergoing vortex-induced vibrations in uniform flow. Motivated by recent engineering applications, we...     

Über die mechanische Kraftwirkung an der Conductoroberfläche

Ohne Zusammenfassung     

Zu v. Pettenkofer's Methode der Kohlens?urebestimmung

Ohne Zusammenfassung     

13C-NMR. Spectroscopy of naturally occurring substances. XLV. Iboga alkaloids.

The carbon shifts of the Iboga-type alkaloids catharanthine, voacangine, coronaridine, ibogaine, dihydrocatharanthine and epiibogamine were recorded and correlated with the conformation of the natural bases. A ¹³C-NMR. analysis of heyneanine determined its C(19) configuration and a similar study of epiheyneanine proved its structure.