Synthesis of some novel functionalized dihydropyrido[2,3-d]pyrimidines via an one-pot three-component reaction catalysed by InCl3

Some novel functionalized dihydropyrido[2,3-d]pyrimidine derivatives 4 were synthesized using a one-pot three-component reaction of 6-aminouracils 1, aryl aldehydes 2 and 3-cyanoacetyl indole 3 using InCl₃ as catalyst.     

Holographic Dark Energy in Higher Derivative Gravity with Varying Gravitational Constant

In this paper we investigate the holographic dark energy scenario in higher derivative gravity with a varying gravitational constant. We introduce a kind of energy density from higher derivative gravity which has role of the same as holographic dark energy. We obtain the exact differential equation , which determine the evolution of the dark energy density based on varying gravitational constant G. We also find out a cosmological application of our work by evaluating a relation for the equation of state of dark energy for low redshifts containing varying G correction.     

Deviations from tri-bimaximal neutrino mixing using type II seesaw

We study the possibility of generating deviations from tri-bimaximal (TBM) neutrino mixing to explain the non-zero reactor mixing angle within the framework of both type I and type II seesaw mechanisms. The type I seesaw term gives rise to the μ–τ   symmetric TBM pattern of neutrino mass matrix as predicted by generic flavor symmetry models like _A4$A_4$ whereas the type II seesaw term gives rise to the required deviations from TBM pattern to explain the non-zero _θ13${\theta }_{13}$. Considering extremal values of Majorana CP phases such that the neutrino mass eigenvalues have the structure (_m1,−_m2,_m3)$(m_1,-m_2,m_3)$ and (_m1,_m2,_m3)$(m_1,m_2,m_3)$, we numerically fit the type I seesaw term by taking oscillation as well as cosmology data and then compute the predictions for neutrino parameters after the type II seesaw term is introduced. We consider a minimal structure of the type II seesaw term and check whether the predictions for neutrino parameters lie in the 3σ range. We also outline two possible flavor symmetry models to justify the minimal structure of the type II seesaw term considered in the analysis.     

Half-Metallic Ferromagnetism in the Co-Doped CdS Diluted Magnetic Semiconductor

JETP Letters - The magnetic properties of Co-doped CdS has been investigated by ab initio calculations using the GGA + U approximation. The study reveals the ferromagnetic ordering of Co-doped CdS...     

Carbon-13 NMR relaxation and transitions in polymers

High-resolution proton-decoupled carbon-13 nuclear magnetic resonance relaxation parameters have been obtained as a function of temperature for a set of completely amorphous polymers, semicrystalline polymers, and a series of ethylene–vinyl acetate copolymers. With these samples the nature of the glass temperature, other postulated amorphous transitions, and the β transition were investigated. For the completely amorphous polymers, the average correlation times depend on temperature according to the Williams–Landel–Ferry relation. Spectral collapse occurs at temperatures whose ratio to T_g is in the range 1.2–1.4 and corresponds to a correlation time of about 10^?7s. The loss of resolvable spectra is demonstrated to be a consequence of experimental methods and is not due to the occurrence of another amorphous transition. Both the methylene and methine carbons can be resolved for the ethylenevinyl acetate copolymers. Although the correlation time for the methylene carbon is continuous and resolvable through the β transition region, the methine branch-point resonance is lost. The implication of these results to the molecular nature of the β transition is discussed.     

Diethyldisulfoammonium chlorometallates as heterogeneous Brønsted–Lewis acidic catalysts for one‐pot synthesis of 14‐aryl‐7‐(N‐phenyl)‐14H‐dibenzo[a,j]acridines

A new series of Brønsted–Lewis acidic diethyldisulfoammonium chlorometallates, [DEDSA][FeCl₄] and [DEDSA]₂[Zn₂Cl₆], were synthesized as solid materials from the reaction of [(Et)₂N(SO₃H)₂][Cl] ionic liquid with transition metal chlorides (FeCl₃ and ZnCl₂) at 80 °C in neat condition for 2 h. The chlorometallates were fully characterized using various spectroscopic and analytical techniques such as Fourier transform infrared, UV–visible and Raman spectroscopies, powder X‐ray diffraction, scanning electron microscopy, energy‐dispersive X‐ray and thermogravimetric analyses, Hammett acidity and elemental analyses. Their catalytic activity was studied as reusable heterogeneous catalysts for the three‐component synthesis of novel 14‐aryl‐7‐(N‐phenyl)‐14H‐dibenzo[a,j]acridines under solvent‐free conditions at 100 °C.     

Aza-Michael Addition of Amines to α,β-Unsaturated Compounds Using Molecular Iodine as Catalyst

Aza-Michael adducts are obtained in very good yields by the conjugate addition of aliphatic amines to α,β-unsaturated compounds using molecular iodine as catalyst in dichloromethane at room temperature. Aromatic amines were found to be reactive under reflux in toluene.     

Effect of E × B electron drift and plasma discharge in dc magnetron sputtering plasma

Study of electron drift velocity caused by Etimes B motion is done with the help of a Mach probe in a dc cylindrical magnetron sputtering system at different plasma discharge parameters like discharge voltage, gas pressure and applied magnetic field strength. The interplay of the electron drift with the different discharge parameters has been investigated. Strong radial variation of the electron drift velocity is observed and is found to be maximum near the cathode and it decreases slowly with the increase of radial distance from the cathode. The sheath electric field, E measured experimentally from potential profile curve using an emissive probe is contributed to the observed radial variation of the electron drift velocity. The measured values of the drift velocities are also compared with the values from the conventional theory using the experimental values of electric and magnetic fields. This study of the drift velocity variation is helpful in providing a useful insight for determining the discharge conditions and parameters for sputter deposition of thin film.     

Selectivity in the Ligand Functionalization of Photocatalytic Metal Oxide Nanoparticles for Phase Transfer and Self-Assembly Applications

The functionalization of photocatalytic metal oxide nanoparticles of TiO₂, ZnO, WO₃ and CuO with amine-terminated (oleylamine) and thiol-terminated (dodecane-1-thiol) alkyl-chain ligands was studied under ambient conditions. A high selectivity was observed in the binding specificity of a ligand towards nanoparticles of these different oxides. It was observed that oleylamine binds stably to only TiO₂ and WO₃, whereas dodecane-1-thiol binds stably only to ZnO and CuO. Similarly, polar-to-nonpolar solvent phase transfer of TiO₂ and WO₃ nanoparticles could be achieved by using oleylamine, but not dodecane-1-thiol, whereas the opposite holds for ZnO and CuO. The surface chemistry of ligand-functionalized nanoparticles was probed by attenuated total reflectance (ATR)-FTIR spectroscopy, which enabled the occupation of the ligands at the active sites to be elucidated. The photostability of the ligands on the nanoparticle surface was determined by the photocatalytic self-cleaning properties of the material. Although TiO₂ and WO₃ degrade the ligands within 24 h under both UV and visible light, ligands on ZnO and CuO remain unaffected. The gathered insights are also highly relevant from an application point of view. As an example, because the ligand-functionalized nanoparticles are hydrophobic in nature, they can be self-assembled at the air-water interface to give nanoparticle films with demonstrated photocatalytic as well as anti-fogging properties.     

A vanadyl complex grafted to periodic mesoporous organosilica: a green catalyst for selective hydroxylation of benzene to phenol

Selective benzene hydroxylation: A periodic mesoporous organosilica embedded with a vanadyl(IV) acetylacetonate complex has been synthesized through a co-condensation method. This system is a catalyst for direct hydroxylation of benzene to phenol, presenting a selectivity of 100?% towards the phenol formation as well as an excellent catalytic recyclability (see scheme).