10 research outputs found

    On the Relativistic Separable Functions for the Breakup Reactions

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    In the paper the so-called modified Yamaguchi function for the Bethe-Salpeter equation with a separable kernel is discussed. The type of the functions is defined by the analytic stucture of the hadron current with breakup - the reactions with interacting nucleon-nucleon pair in the final state (electro-, photo-, and nucleon-disintegration of the deuteron).Comment: 4 pages, 2 figures, to be published in EPJ Wo

    The Separable Kernel of Nucleon-Nucleon Interaction in the Bethe-Salpeter Approach

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    The dispersion relations for nucleon-nucleon (NN) T-matrix in the framework of Bethe-Salpeter equation for two spin one-half particle system and with separable kernel of interaction are considered in the paper. The developed expressions are applied for construction of the separable kernel of interaction for S partial-waves in singlet and triplet channels. We calculate the low energy scattering parameters and the phase shifts and also the deuteron binding energy with the separable interaction. The approach can be easily extended to higher partial-waves for NN-scattering and other reactions (anti N N-, pi N-scattering).Comment: RevTex 4 style, 9 pages, 1 figur

    On the Relativistic Separable Functions for the Breakup Reactions

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    In the paper the so-called modified Yamaguchi function for the Bethe-Salpeter equation with a separable kernel is discussed. The type of the functions is defined by the analytic stucture of the hadron current with breakup - the reactions with interacting nucleon-nucleon pair in the final state (electro-, photo-, and nucleon-disintegration of the deuteron)

    4,5-Bis(dimethylamino)quinolines: Proton Sponge versus Azine Behavior

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    Two first representatives, <b>5</b> and <b>6</b>, of the still unknown 4,5-bis(dimethylamino)quinoline have been synthesized and studied. While the former, being protonated either at the peri-NMe<sub>2</sub> groups or at the ring nitrogen, has been shown to display properties of both a proton sponge and azine, its counterpart <b>6</b> behaves exclusively as azine giving only a quinolinium salt

    4,5-Bis(dimethylamino)quinolines: Proton Sponge versus Azine Behavior

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    Two first representatives, <b>5</b> and <b>6</b>, of the still unknown 4,5-bis(dimethylamino)quinoline have been synthesized and studied. While the former, being protonated either at the peri-NMe<sub>2</sub> groups or at the ring nitrogen, has been shown to display properties of both a proton sponge and azine, its counterpart <b>6</b> behaves exclusively as azine giving only a quinolinium salt

    4,5-Bis(dimethylamino)quinolines: Proton Sponge versus Azine Behavior

    No full text
    Two first representatives, <b>5</b> and <b>6</b>, of the still unknown 4,5-bis(dimethylamino)quinoline have been synthesized and studied. While the former, being protonated either at the peri-NMe<sub>2</sub> groups or at the ring nitrogen, has been shown to display properties of both a proton sponge and azine, its counterpart <b>6</b> behaves exclusively as azine giving only a quinolinium salt
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