Here is presented the top-quark pair plus photon production cross section measured in pp collisions at a centre-of-mass energy of √ s = 8 TeV with the CMS detector at the Large Hadron Collider, using data recorded in 2012 corresponding to an integrated luminosity of Lint = 19:6 fb−1. The measurement is performed in the dilepton decay channel. The fiducial region is defined by the final state of the process pp → W⁺W⁻b bl γ, with a minimum photon transverse energy of ET( γ) > 25 GeV and lies within a pseudorapidity range of η ( γ)| < 1:4442, with a separation of ∆R(γ; all) > 0:3 between the photon and quarks or leptons in η - space. Signal events are simulated using the MadGraph event generator. Data-driven templates are constructed in order to measure the photon identification efficiency using the supercluster footprint removal technique, and a fit to the charged hadron isolation is performed. The ratio of tt + γ cross section relative to the inclusive t t cross section, R = t t+ t t, is exploited in order to cancel various sources of systematic uncertainties. The combination of dilepton final state decay channels ratio in the fiducial area is measured to be R = 0:00115 ± 0:00023(stat:). Using a recent CMS t t cross section measurement at 8 TeV in the dilepton channel of t t = 245:6± 1:3(stat:)± +6:6/5:5 (syst:) ± 6:5(lumi:) pb, the top pair plus photon production cross section is calculated to be CMS / t t+γ = 944 154(stat:+syst:) fb. Being in agreement with the t t+γ SM expectation of SM / t t+γ = 861 ± 71(scale) ± 30(PDF) fb, this is the most accurate measurement of the t t +γ process to date, and the first at a centre-of-mass energy of 8 TeV in the dilepton channel.

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A thesis submitted to the Faculty of Science, University of the Witwatersrand, Johannesburg, in fulfilment of the requirements for the degree of Doctor of Philosophy. Johannesburg, December 2014. / In this thesis the evolution equations of the Yukawa couplings and quark flavour mixings are derived for the one-loop renormalisation group equations in five and six-dimensional models, compactified in different possible ways to yield standard four space-time dimensions. Different possibilities for the matter fields are discussed, such as the case of bulk propagating or brane localized fields. We discuss in both cases the evolution of the Yukawa couplings, the Jarlskog parameter and the Cabibbo-Kobayashi-Maskawa matrix elements, finding that for both scenarios, as we run up to the unification scale, significant renormalisation group corrections are present. We also discuss the results of different observables of the five-dimensional universal extra dimension model in comparison with those of six-dimensional models and the model dependence of the results. We also studied the scaling of the mass ratios and the implications for the mixing angles in these six-dimensional model as well as the 5D Minimal Supersymmetric Standard Model on an S1/Z2 orbifold. The renormalisation group equation evolutions for the Higgs sector and for the neutrino sector in six-dimensional models are also investigated. The recent experimental results of the Higgs boson from the LHC allow, in some scenarios, stronger constraints on the cutoff scale to be placed, from the requirement of the stability of the Higgs potential.

Thesis (M.S.)--Mississippi State University. Department of Mechanical Engineering. / Title from title screen. Includes bibliographical references.

The study consists of three major areas of research. First, the dihedral angle dependence of vicinal carbon-carbon coupling constants is determined for aliphatic and alicyclic carboxylic acids wherein the formal hybridization and substituents are held constant. Second, the magnitudes and relative signs of long-range carbon-carbon coupling constants in a. triple- 13 C-labeled system are determined and compared with carbon-proton and/or proton-proton coupling constants in geometrically similar compounds. Third, the effect of changes in hybridization on long-range carbon-carbon coupling constants is determined for the following three groups of molecules: olefins and saturated hydrocarbons, aliphatic carboxylic acids, and aromatic compounds. In all cases only closely related systems are compared in order to identify the effect of individual molecular parameters. Most importantly, the results indicate that carbon-carbon couplings do correlate in magnitude and sign with carbon-proton and proton-proton couplings in analogous molecular. frameworks. Thus, the coupling mechanisms are similar in all three types of coupling. In addition, the observed trends in long-range carbon-carbon couplings provide an unambiguous method for assigning carbon chemical shifts.

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