4,132 research outputs found
Soft gluon resummation in the signal-background interference process of
We present a precise theoretical prediction for the signal-background
interference process of , which is useful to constrain the
Higgs boson decay width and to measure Higgs couplings to the SM particles. The
approximate NNLO -factor is in the range of (),
depending on , at the 8 (13) TeV LHC. And the soft gluon resummation
can increase the approximate NNLO result by about at both the 8 TeV and
13 TeV LHC. The theoretical uncertainties including the scale, uncalculated
multi-loop amplitudes of the background and PDF are roughly
at . We also confirm that the approximate
-factors in the interference and the pure signal processes are the same.Comment: 18 pages, 9 figures; v2 published in JHE
Search for the signal of monotop production at the early LHC
We investigate the potential of the early LHC to discover the signal of
monotops, which can be decay products of some resonances in models such as
R-parity violating SUSY or SU(5), etc. We show how to constrain the parameter
space of the models by the present data of boson hadronic decay branching
ratio, mixing and dijet productions at the LHC. Then, we study
the various cuts imposed on the events, reconstructed from the hadronic final
states, to suppress backgrounds and increase the significance in detail. And we
find that in the hadronic mode the information from the missing transverse
energy and reconstructed resonance mass distributions can be used to specify
the masses of the resonance and the missing particle. Finally, we study the
sensitivities to the parameters at the LHC with =7 TeV and an
integrated luminosity of in detail. Our results show that the
early LHC may detect this signal at 5 level for some regions of the
parameter space allowed by the current data.Comment: 25 pages, 18 figures, 3 tables, version published in Phys.Rev.
(E)-3-(1-Methyl-1H-pyrrol-2-yl)-1-phenylÂprop-2-en-1-one
The crystal structure of the title compound, C14H13NO, exhibits an E configuration. The conjugated compound is slightly twisted with a dihedral angle of 29.3° between the benzene and pyrrole rings. Two interÂmolecular C—H⋯O interÂactions lead to a dimer. In the crystal, intermolecular C—H⋯O interactions generate an inversion dimer
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