Does the HyperCP evidence for the decay Sigma+ -->pmu+mu- indicate a light pseudoscalar Higgs boson?

The HyperCP Collaboration has observed three events for the decay Sigma+ -->p mu+mu- which may be interpreted as a new particle of mass 214.3 MeV. However, existing data from kaon and B-meson decays provide stringent constraints on the construction of models that support this interpretation. In this Letter we show that the "HyperCP particle" can be identified with the light pseudoscalar Higgs boson in the next-to-minimal supersymmetric standard model, the A10. In this model there are regions of parameter space where the A10 can satisfy all the existing constraints from kaon and B-meson decays and mediate Sigma+ -->p mu+mu- at a level consistent with the HyperCP observation.     

Improving the sensitivity of cellulose fiber-based lateral flow assay by incorporating a water-dissolvable polyvinyl alcohol dam

Cellulose - Lateral flow assay (LFA) is an important point-of-care (POC) test platform due to the associated portability, on-site testing, and low cost for diagnosis of pathogen infections and...     

Oxidation of aromatic sulfides with molecular oxygen: Controllable synthesis of sulfoxides or sulfones

The recent development of selective oxidation of aromatic sulfides with molecular oxygen was highlighted. The sulfoxides and sulfones could be obtained by simply switching the reaction media, i.e., bis(2-butoxyethyl)ether (BBE) or poly(ethylene glycol)dimethyl ether (PEGDME). The application of the high-boiling-point polyether as an initiator and green media can eliminate the need of large quantities of additives and volatile solvents. This strategy represents an economic and eco-friendly method that could find potential applications.     

Syntheses and Crystal Structures of Two New Pentaborates Templated by Transition-Metal Complexes

Two new pentaborates [M(dap)₃][B₅O₆(OH)₄]₂·H₂O (M = Co (1) and Ni (2); dap = 1,2-diaminopropane) have been hydrothermally synthesized. Both structures were determined by single crystal X-ray diffraction and further characterized by elemental analysis, FT-IR, thermogravimetric analysis and photoluminescence spectroscopy. Two compounds are isostructural and consist of isolated pentaborate [B₅O₆(OH)₄]^? anions and [M(dap)₃]²⁺ complex cations. The anionic [B₅O₆(OH)₄]^? groups are linked by extensive hydrogen bonds to form a 3-D supramolecular framework with large channels, in which the transition-metal complex templates are located. The luminescent properties of 1 and 2 were studied, and blue luminescence occurs with an emission maximum at 405 and 408 nm upon excitation at 332 and 328 nm respectively. Crystal data: 1, monoclinic, space group P2₁/c (No. 14), a = 9.7159(5) Å, b = 29.3372(19) Å, c = 11.5121(6) Å, β = 103.286(5)°, V = 3193.6(3) ų, Z = 4; 2, monoclinic, space group P2₁/c, a = 9.7264(4) Å, b = 29.3810(16) Å, c = 11.5185(6) Å, β = 103.249(4)°, V = 3204.0(3) ų, Z = 4.     

Coloring properties of novel 1,4-distyrylbenzene and 4,4′-distyrylbiphenyl fluorescent brighteners and their arrangement in cotton and polyester fiber

Some novel 1,4-distyrylbenzene (DSB) and 4,4′-distyrylbiphenyl (DSBP) fluorescent brighteners (FBs) were used to dye polyester and cotton fabrics. The CIE whiteness, color hue and reflectance spectrum of dyed fabrics were compared. DSBP derivatives could dye the cotton and polyester fabrics with a higher whiteness level and had a lower fluorescent quenching concentration than DSB derivatives. The color hue for the fabric dyed with DSB FBs was yellow-green, whereas that dyed with DSBP was blue–violet. The molecular arrangement in the fiber had a significant influence on their optical properties, resulting in different coloring properties. The increase in molecule planarity and rigidity generated by the interaction between the polymer and FB molecules caused a remarkable bathochromic shift in emission and excitation spectra. The H-aggregate of the DSB molecule in the fiber was easily generated, and the degree of aggregation increased with the molecular polarity. However, the aggregation of DSBP molecules in the polyester and cotton fiber was not found. The surface region of the cotton fiber was filled with FB molecules, whereas FB molecules in the polyester fiber aggregated easily, and incident light could pass through the surface region.     

The Relationship of Freeze Tolerance with Intracellular Compounds in Baker’s Yeasts

Freeze-tolerant baker’s yeasts are required for the processing of frozen doughs. The present study was carried out to investigate the cell survival rate after frozen storage and the change of fermentability in dough due to frozen storage, and to discuss quantitatively the relationship of freeze tolerance with intracellular trehalose, amino acids, and glycerol, using six types of baker’s yeasts as the test materials. The experimental results showed that the fermentability of yeast cells in frozen dough was strongly correlated with the cell survival rate. The baker’s yeast with a higher level of cell survival rate had a larger increase in the total intracellular compound content after frozen storage, and the cell survival rate increased linearly with increasing total intracellular compound content in frozen yeast cells. Trehalose was a primary compound affecting freeze tolerance, followed by glutamic acid, arginine, proline, asparagic acid, and glycerol. The basic information provided by the present study is useful for exploring the freeze-tolerance mechanisms of baker’s yeast cells, breeding better freeze-tolerant baker’s yeast strains, and developing more effective cryoprotectants.     

Visible-Light-Induced ortho-Selective Migration on Pyridyl Ring: Trifluoromethylative Pyridylation of Unactivated Alkenes

The photocatalyzed ortho-selective migration on a pyridyl ring has been achieved for the site-selective trifluoromethylative pyridylation of unactivated alkenes. The overall process is initiated by the selective addition of a CF₃ radical to the alkene to provide a nucleophilic alkyl radical intermediate, which enables an intramolecular endo addition exclusively to the ortho-position of the pyridinium salt. Both secondary and tertiary alkyl radicals are well-suited for addition to the C2-position of pyridinium salts to ultimately provide synthetically valuable C2-fluoroalkyl functionalized pyridines. Moreover, the method was successfully applied to the reaction with P-centered radicals. The utility of this transformation was further demonstrated by the late-stage functionalization of complex bioactive molecules.     

Thermal hazard assessment and ranking for organic peroxides using quantitative structure–property relationship approaches

Journal of Thermal Analysis and Calorimetry - Chemical reactivity hazards of organic peroxides are major concerns of the chemical industry due to many serious incidents every year. Thermal hazard...     

Enantioselective three-component Ugi reaction catalyzed by chiral phosphoric acid

A catalytic enantioselective three-component Ugi reaction was developed. SPINOL-derived phosphoric acid with bulky 2,4,6-tricyclohexylphenyl groups at the 6,6′ positions was found to be the best catalyst to afford α-amino amide derivatives in good to excellent yields(62% to 99%) and enantiocontrol(81% to 99% enantiomeric excess). This asymmetric reaction was applicable well to an array of aliphatic aldehydes. The gram-scale synthesis, modification of dapsone, and enantioselective synthesis of(R)-Lacosamide underline the general utility of this methodology. Influence of dihedral angles and substituents of the chiral phosphoric acids on the enantioselectivity was also discussed in this article.