Bifunctional catalytic/magnetic Ni@Ru core-shell nanoparticles

Core-shell structured Ni@Ru bimetallic nanoparticles are demonstrated as a bifunctional nanoplatform system for the hydrolysis reaction of ammonia-borane and also for magnetic separation.     

TheK-conversion coefficient of the 321 keVE1 transition in Hf177

TheK-conversion coefficient of the 321 keVE1 transition in Hf¹⁷⁷ has been measured by means of an iron free double focusing beta-ray spectrometer, using the internalexternal conversion method. The result obtained for α _K (321)=0.162±0.016 is in disagreement with the theoretical values for pureE1 transition (α _K =0.0154) calculated bySliv andBand. The large anomaly observed in theK-conversion process of the inhibitedE1 transition is compatible with a largeM2 admixture or, more probable with the presence of penetration matrix elements.     

G-espaces topologiques

In this paper we define a topologicalG-space, whereG is a monoid, and we extend the notion of bounded sets in this spaces.     

Magnetic moments of85–90Y nuclei

Low temperature nuclear orientation (LTNO) of neutron deficient^{85m, 86m+}g,^{87m, 90m}Y nuclei is described. The magnetic moments are compared with those of neighbouring nuclei.     

Darstellung und eigenschaften von und reaktionen mit metallhaltigen heterocyclen: XXXIII. Synthese und kristallstruktur von (μ3-thio)(μ3-organophosphido)tris(tricarbonyleisen)-(2Fe-Fe)-komplexen

The cluster compounds (μ₃-S)(μ₃-PR)Fe₃(CO)₉ are obtained by reaction of the dichloroorganylphosphane sulphides RP(S)Cl₂ (R = CH₃, 4-CH₃OC₆H₄, C₆H₅) with Na₂[Fe(CO)₄] in ether under cleavage of the PS bond. On the basis of X-ray crystallographic determinations the iron clusters crystallize for R = 4-CH₃OC₆H₄ and C₆H₅ in the monoclinic and triclinic space group C2/c and P$\text{1}$ with Z = 8 and 4, respectively.     

Running of neutrino parameters and the Higgs self-coupling in a six-dimensional UED model

We investigate a six-dimensional universal extra-dimensional model in the extension of an effective neutrino mass operator. We derive the β  -functions and renormalization group equations for the Yukawa couplings, the Higgs self-coupling, and the effective neutrino mass operator in this model. Especially, we focus on the renormalization group running of physical parameters such as the Higgs self-coupling and the leptonic mixing angles. The recent measurements of the Higgs boson mass by the ATLAS and CMS Collaborations at the LHC as well as the current three-flavor global fits of neutrino oscillation data have been taken into account. We set a bound on the six-dimensional model, using the vacuum stability criterion, that allows five Kaluza–Klein modes only, which leads to a strong limit on the cutoff scale. Furthermore, we find that the leptonic mixing angle _θ12${\theta }_{12}$ shows the most sizeable running, and that the running of the angles _θ13${\theta }_{13}$ and _θ23${\theta }_{23}$ are negligible. Finally, it turns out that the findings in this six-dimensional model are comparable with what is achieved in the corresponding five-dimensional model, but the cutoff scale is significantly smaller, which means that it could be detectable in a closer future.     

Demonstration of image-zooming capability for diffractive axicons

Diffractive axicons are optical components producing achromatic nondiffracting beams. They thus produce a focal line rather than a focal point for classical lenses. This gives the interesting property of a long focal depth. We show that this property can be used to design a simple imaging system with a linear variable zoom by using and translating a diffractive axicon as the only optical component.     

Synthesis and mesomorphism behaviour of chalcones and pyrazoles type compounds as photo-luminescent materials

The following organic and organic–inorganic hybrid compounds were prepared as photo-luminescent materials following efficient and practical synthetic methods: 1,3-bis[4-(n-alkoxy)phenyl]-2-propen-1-one (where, n-alkoxy: O(CH₂)_nH, n = 6,7,8,9 or 10); 3,5-bis[4-(n-alkoxy)phenyl]-1H-pyrazole (where, n-alkoxy: O(CH₂)_nH, n = 6,7,8,9 or 10) (in case of n = 7, a mixture of 3,5-bis(4-heptyloxyphenyl)-1H-pyrazole and 3,5-bis(4-heptyloxyphenyl)-4H-pyrazole was detected) and bis(3,5-bis [4-(n-alkoxy) phenyl]-1H-pyrazole) silver(I) nitrate (where, n-alkoxy: O(CH₂)_nH, n = 6,7,8,9 or 10). The prepared compounds have been characterised and their structures were elucidated depending upon (FTIR, UV-Vis, ¹HNMR, ¹³CNMR, 2D ¹H-¹H-COSY, 2D ¹H-¹³C-HSQC and mass spectra) in addition to molar conductivity measurements for silver(I) complexes. The mesomorphism behaviour of the prepared compounds was studied using polarised light optical microscopy and confirmed with differential scanning calorimetry and X-ray powder diffraction techniques. The studies showed that among all of these compounds only the pyrazole derivatives are liquid crystal materials. The luminescent properties of all the prepared compounds were also investigated which confirmed that all of these compounds are photo-luminescent in the crystalline solid state and in the mesophase.