The impossibility of heavy neutrino dark matter in the Littlest Higgs Model with T-parity: Constraints from direct search

We consider the Littlest Higgs Model with T-parity (LHT), in the parameter region where a heavy neutrino is the lightest T-odd particle (LTP). Having emphasized that this corresponds to a sizable region in the parameter space of the theory, we show that both the Cryogenic Dark Matter Search (CDMS) and Xenon10 experiments disallow the entire region where the masses of the new particles in LHT can lie within several TeV. Therefore, any observation of the signals of a heavy neutrino LTP is likely to seriously reopen the issue of cold dark matter in the universe.     

Synthesis of carbon nanotubes by catalytic vapor decomposition (CVD) method: Optimization of various parameters for the maximum yield

This paper describes an effect of flow rate, carrier gas (H₂, N₂ and Ar) composition, and amount of benzene on the quality and the yield of carbon nanotubes (CNTs) formed by catalytical vapour dcomposition (CVD) method. The flow and mass control of gases and precursor vapors respectively were found to be interdependent and therefore crucial in deciding the quality and yield of CNTs. We have achieved this by modified soap bubble flowmeter, which controlled the flow rates of two gases, simultaneously. With the help of this set-up, CNTs could be prepared in any common laboratory. Raman spectroscopy indicated the possibilities of formation of single-walled carbon nanotubes (SWNTs). From scanning electron microscopy (SEM) measurements, an average diameter of the tube/bundle was estimated to be about 70 nm. The elemental analysis using energy dispersion spectrum (EDS) suggested 96 at.wt.% carbon along with ca. 4 at.wt.% iron in the as-prepared sample. Maximum yield and best quality CNTs were obtained using H₂ as the carrier gas.      

Enhancement of oxygen and methane solubility in 1-hexyl-3-methylimidazolium bis(trifluoromethylsulfonyl) imide using carbon dioxide

The presence of CO(2) increases the solubility of O(2) and CH(4) in 1-hexyl-3-methylimidazolium bis(trifluoromethylsulfonyl) imide at 25 degrees C and pressures to 13 bar.     

Polyimides from diisocyanates and dianhydride

Polyimides soluble in polar solvents such as dimethylacetamide (DMAC) and dimethylformamide (DMF) were synthesized by reacting 3,3′,4,4′-benzophenonetetracarboxylic dianhydride (BTDA) and three different diisocyanates with the following general structure: where R is ethyl, propyl, or phenyl. Thermal properties of these polymides have been compared with that obtained by reacting 2,2-bis(4-isocyanatophenyl)propane and BTDA.     

A generalized VMD mechanism for radiative decays of cc mesons

A generalized VMD mechanism, implemented through the OPC model, is proposed for E1 and M1 decays of $\text{c}\text{c}$ mesons wherein the photon couples to two infinite sequences of radial excitations of ³S₁ and ³D₁$\text{c}\text{c}$ states. The results reveal good accord with data under the conventional assignments, with a parameter signifying a reduced magnetic coupling of ψ-ions with c quarks.     

Lattice-dynamical calculations of the thermodynamic properties of CsBr and CsI

Results of a quasi-harmonic calculation of the normal mode frequencies, mode-Grüneisen parameters, the coefficient of thermal expansion α, the heat capacity C_p, and the macroscopic Grüneisen function γ(itT) for CsBr and CsI are presented. Very good agreement with the experimental results for α and C_p is obtained. A self-consistent procedure is used to parametrize the models so that some often neglected vibrational and configuration-dependent effects can be accounted for. Predictions are made for the values that the potential energy derivatives and the elastic constants would have in the absence of vibrational motion.     

Development and validation of UPLC tandem mass spectrometry assay for separation of a phase II metabolite of ramipril using actual study samples and its application to a bioequivalence study

In this paper, we present a validated UPLC‐MS/MS assay for determination of ramipril and ramiprilat from human plasma samples. The assay is capable of isolating phase II metabolites (acylglucornides) of ramipril from in vivo study samples which is otherwise not possible using conventional HPLC conditions. Both analytes were extracted from human plasma using solid‐phase extraction technique. Chromatographic separation of analytes and their respective internal standards was carried out using an Acquity UPLC BEH C₁₈ (2.1 × 100 mm), 1.7 µm column followed by mass spectrometric detection using an Waters Quattro Premier XE. The method was validated over the range 0.35–70.0 ng/mL for ramipril and 1.0–40.0 ng/mL for ramiprilat. Copyright © 2010 John Wiley & Sons, Ltd.     

Synthesis and Cation Recognition Study of Novel Benzo Crown Ether Functionalized Enamine Derivatives

A novel series of benzo crown ether (dibenzo 18-crown-6 ether, benzo 18-crown-6 ether, and benzo 15-crown-5 ether) functionalized enamines derivatives from amino benzo crown ether (4-amino dibenzo 18-crown-6 ether, 4-amino benzo 18-crown-6 ether, 4-amino benzo 15-crown-5 ether) and substituted 3-(dimethylamino)-1-phenylprop-2-en-1-one compounds have been synthesized. All the synthesized compounds were characterized by infrared, ¹H NMR, ¹³C NMR, distortionless enhancement polarization transfer, and mass and elemental analysis techniques. The cation recognition property for benzo crown ether enamine 8a was studied by absorption and fluorescence spectroscopy.     

Temperature-Gradient-Directed NMR Monitoring of a [3 + 3]-Cyclocondensation Reaction Between Alkynone and Ethyl 2-Amino-1H-indole-3-carboxylate Toward the Synthesis of Pyrimido[1,2-a]indole Catalyzed by Cs2CO3

We describe a NMR strategy to resolve temperature-gradient-monitored real-time chemical reaction involving a [3 + 3]-cyclocondensation reaction between alkynone and ethyl 2-amino-1H-indole-3-carboxylate toward the synthesis of pyrimido[1,2-a]indole catalyzed by Cs₂CO₃. The in situ NMR study clearly indicates that the reactant undergoes [3 + 3]-cyclocondensation reaction through a concerted mechanism, resulting in the product formation. The detailed NMR spectroscopic data led to the optimization of the reaction conditions and quantitative analysis of the product accurately and efficiently.

Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications® to view the free supplemental file.     

A Review on Obesity Management through Natural Compounds and a Green Nanomedicine-Based Approach

Obesity is a serious health complication in almost every corner of the world. Excessive weight gain results in the onset of several other health issues such as type II diabetes, cancer, respiratory diseases, musculoskeletal disorders (especially osteoarthritis), and cardiovascular diseases. As allopathic medications and derived pharmaceuticals are partially successful in overcoming this health complication, there is an incessant need to develop new alternative anti-obesity strategies with long term efficacy and less side effects. Plants harbor secondary metabolites such as phenolics, flavonoids, terpenoids and other specific compounds that have been shown to have effective anti-obesity properties. Nanoencapsulation of these secondary metabolites enhances the anti-obesity efficacy of these natural compounds due to their speculated property of target specificity and enhanced efficiency. These nanoencapsulated and naive secondary metabolites show anti-obesity properties mainly by inhibiting the lipid and carbohydrate metabolizing enzymes, suppression of adipogenesis and appetite, and enhancing energy metabolism. This review focuses on the plants and their secondary metabolites, along with their nanoencapsulation, that have anti-obesity effects, with their possible acting mechanisms, for better human health.