Radiative muon capture in medium-heavy nuclei

Radiative muon capture in nuclei is thoroughly investigated in view of its sensitivity to the pseudoscalar coupling constant g_P. In the photon energy domain of interest (k ? 60 MeV) the effective one-body hamiltonian in use is shown essentially to hold true, with minor corrections due to the muon propagator in the nuclear field and to the two-step process. The closure approximation is avoided by appropriately integrating the response function calculated in the Fermi gas model, in the energy-momentum transfer plane.Theoretical predictions in medium-heavy nuclei of the high-energy photon spectrum, of photon polarization, and of muon-spin photon angular correlation are given for various values of the pseudoscalar coupling constant.     

Differential Algebra-Based Multiple Gaussian Particle Filter for Orbit Determination

Journal of Optimization Theory and Applications - The nonlinear filtering problem plays a fundamental role in multiple space-related applications. This paper offers a new filtering technique that...     

Ion chemistry of phthalamic acids. 2—mass spectral retrosynthesis of phthalanilic acids and structure analysis of [C8H6NO2]+ ions from N-cyclohexylphthalamic acid and [MH]+ of N-cyclohexylphthalimide

Under electron impact o-phthalanilic acids show the retrosynthetic reaction previously described for other phthalamic acids. As primary amine derivatives they undergo thermal and electron impact induced water loss. Like the molecular ions of the related phthalimides, their [M? H₂O]^+˙ do not give [C₈H₆NO₂]⁺ fragments, which are obtained from the N-cyclohexyl derivative. The structure of such fragments is investigated by collisionally activated mass analysed ion kinetic energy spectra, and compared with the [MH]⁺ of phthalimide, obtained by chemical ionization with CH₄ or NH₃ and assumed to be possible models.     

Syntheses of 2-arylimidazole derivatives through annelations employing benzylamines

Annelations of benzylamines with hydroximino derivatives of pentane-2,4-dione or of alkyl acetoacetates, acetoacetamides, and acetoacetanilides, afford imidazole derivatives and provide easy incorporation of the benzylic carbon and nitrogen in the heterocycle. The limits of the reaction have been explored.