Highly Stereoselective Synthesis of Natural‐Product‐Like Hybrids by an Organocatalytic/Multicomponent Reaction Sequence

In an endeavor to provide an efficient route to natural product hybrids, described herein is an efficient, highly stereoselective, one‐pot process comprising an organocatalytic conjugate addition of 1,3‐dicarbonyls to α,β‐unsaturated aldehydes followed by an intramolecular isocyanide‐based multicomponent reaction. This approach enables the rapid assembly of complex natural product hybrids including up to four different molecular fragments, such as hydroquinolinone, chromene, piperidine, peptide, lipid, and glycoside moieties. The strategy combines the stereocontrol of organocatalysis with the diversity‐generating character of multicomponent reactions, thus leading to structurally unique peptidomimetics integrating heterocyclic, lipidic, and sugar moieties.     

Phase equilibrium data for the ternary system (propane + chloroform + oryzanol)

The compound oryzanol available in the rice bran (oriza sativa) is well known for its antioxidant activity. Phase equilibrium data involving oryzanol in compressed fluids, hardly found in the literature, are important to provide the basis for the extraction and fractionation processes. In this sense, the aim of this work is to report phase equilibrium measurements for the system (γ-oryzanol + chloroform) in compressed propane. Phase equilibrium experiments were performed using the static synthetic method (cloud points transition data) in a high-pressure variable-volume view cell in the temperature range of 303 K to 353 K, pressures up to 17 MPa, for oryzanol overall mass fractions of 2 wt%, 5 wt% and 10 wt% in (propane + chloroform) mixtures. A complex phase behaviour comprising vapour–liquid, liquid–liquid, vapour–liquid–liquid, solid–liquid, solid–liquid–liquid, solid–liquid–liquid–vapour transitions were visually observed for the system studied.     

Electrokinetic properties of wavellite and its floatability with cationic and anionic collectors

The reverse apatite flotation with fatty acids has been widely used for the reduction of phosphorus content of magmatic origin iron ores. However, the occurrence of phosphorus intensely disseminated as secondary minerals such as wavellite renders the anionic reverse flotation a challenge. Zeta potential measurements and microflotation tests of wavellite with the use of anionic and cationic collectors were carried out in this work. The wavellite's IEP value was achieved at pH 4.5. Below the IEP value, the surface positively charged sites are made up of aluminum ions. The species H(+), Al(OH)(2)(+), Al(OH)(2+), Al(3+), OH(-), H(2)PO(4)(-), HPO(4)(2-), and PO(4)(3-) play a role in the protonation and deprotonation reactions that will determine the wavellite-solution interface properties. The highest values of wavellite's floatability under basic pH conditions were achieved in the presence of cationic collectors (1 × 10(-4) mol L(-1)). The formation of surface complexes and the precipitation of insoluble salt of aluminum onto wavellite surface seems to be the most likely hypothesis for the chemical nature interactions between amines and wavellite. The surface formation of aluminum oleate on the wavellite's surface seems to be the most probable hypothesis for the adsorption mechanism and the resultant high floatability of wavellite between pH 7.5 and pH 10.0 in the presence of sodium oleate (1 × 10(-4) mol L(-1)). The results showed that the cationic reverse flotation of secondary phosphates is a promising route to reduce the phosphorus content of iron ores from deposits that underwent a supergene enrichment process, since wavellite floatability in the alkaline pH range, using amine as collector, was not significantly affected by the presence of corn starch.     

Tetrachlorocarbonyliridates: water-soluble carbon monoxide releasing molecules rate-modulated by the sixth ligand

A new family of compounds is presented as potential carbon monoxide releasing molecules (CORMs). These compounds, based on tetrachlorocarbonyliridate(III) derivatives, were synthesized and fully characterized by X-ray diffraction, electrospray mass spectrometry, IR, NMR, and density functional theory calculations. The rate of CO release was studied via the myoglobin assay. The results showed that the rate depends on the nature of the sixth ligand, trans to CO, and that a significant modulation on the release rate can be produced by changing the ligand. The reported compounds are soluble in aqueous media, and the rates of CO release are comparable with those for known CORMs, releasing CO at a rate of 0.03-0.58 μM min(-1) in a 10 μM solution of myoglobin and 10 μM of the complexes.     

Reversible hydrocarbon/perfluorocarbon phase-switching of [Ru(bipy)3]2+ driven by supramolecular heteromeric fluorous carboxylate-carboxylic acid H-bond interactions

The Ru(bipy)(3) dication is efficiently and reversibly transferred into perfluorocarbons due to the formation of a highly fluorophillic hydrogen-bonded fluorous carboxylate-carboxylic acid counter-anion, whilst retaining key luminescence and photosensitizer characteristics, for example in singlet oxygen production.     

Operation of a 32 GHz gyrotron

The design and operation of a 32 GHz pulsed gyrotron are reported. The device is step-tuned between the TE_1,2 (24.16 GHz) and TE_0,2 (31.78 GHz) modes with cathode voltages ranging from 30 to 40kV and beam current up to 5.0A. Experimental frequencies are in close agreement with the self-consistent calculated values and in the TE_2,2 resonator mode an output peak power of 6kW corresponding to an 18% efficiency was measured by using a fast response calorimeter with a thermal sensitivity of 0.1°C/Wmin.     

57Fe Mössbauer investigation of the ternary hydride Pd3FeHx

Ordered alloys of Pd₃Fe are shown to readily absorbe hydrogen through electrolytic loading. The resultant ternary hydride phase is observed to retain the fcc structure of Pd₃Fe with approximately the same lattice constant. The ⁵⁷Fe hyperfine field determined by Mössbauer spectroscopy is found to be 30% smaller in the hydride compared to Pd₃Fe. The reduction appears to be associated with a perturbation of the Pd moment by hydrogen. The results suggest the occupation of one type of interstitial site in the structure. The absence of the site in disordered Pd₃Fe would explain the much smaller hydrogen capacity observed for this alloy.     

相对论性核碰撞中φ介子增强

用强子和弦级联模型LUCIAE系统地研究了相对论性p+p和Pb+Pb碰撞中φ介子产生.在模型框架内实验测得的158AGeV/cPb+Pb碰撞中φ介子产额相对于同能量p+p碰撞的增强现象,依赖于弦发射胶子的集体效应和奇异夸克压低约化两机制,在一定程度内能得到解释.     

在RHIC的极限碎裂和Ф介子产生(英文)

利用强子和串级联模型LUCIAE研究了PHOBOS的极限碎裂等以及在PHIC进行的Au +Au碰撞中带电粒子多重性的经验标度规律 .对介子的产生机制也通过与带电粒子多重性的比较进行类似的研究 .结果似乎表明在串级碎裂模型中带电粒子和介子有共同的产生机制 .还讨论了PHOBOS经验标度规律的模型依赖性 .