Brown HT

Journal of Thermal Analysis and Calorimetry - Thermal behavior of Brown HT food dye was studied in correlation with the physical and biological antioxidant properties. Brown HT’s structure...     

Tartrazine: physical,thermal and biophysical properties of the most widely employed synthetic yellow food-colouring azo dye

Journal of Thermal Analysis and Calorimetry - The food-colouring dye tartrazine is a significant additive and in the same time a biologically active material. Thermal behaviour of trisodium...     

Supersymmetry breaking

We review the various mechanisms of supersymmetry breaking and its transmission to the observable sector. We argue that hybrid models where gauge dominates over gravity mediation, but gravity provides the main contributions to the Higgs sector masses and the neutralino mass, are able to combine the advantages and reduce the disadvantages of the two transmission mechanisms.      

Nonlinear supersymmetry and goldstino couplings to the MSSM

We briefly review the nonlinear supersymmetry formalisms in the standard realization and superfield methods. We then evaluate the goldstino couplings to the minimal supersymmetric standard model (MSSM) superfields and discuss their phenomenological consequences. These relate to the tree-level Higgs mass and to invisible Higgs- and Z-boson decays. The Higgs mass is increased from its MSSM tree-level value and brought above the LEP2 mass bound for a low scale of supersymmetry breaking √f ∼ 2 TeV to 7 TeV. The invisible decay rates of the Higgs and Z bosons into goldstino and neutralino are computed and shown to bring stronger constraints on f than their decays into goldstino pairs, which are subleading in 1/f.     

A Novel Approach for the Synthesis of 5‐Pyridylindolizine Derivatives via 2‐(2‐Pyridyl)pyridinium Ylides

New indolizine derivatives were synthesized by an efficient one‐pot three‐component procedure starting from commercially available materials such as 2,2′‐dipyridyl, substituted bromoacetophenones, and electron‐poor alkynes in 1,2‐epoxybutane as reaction solvent and acid scavenger.