Solid solution of transition metal-dicarboxylates with tunable magnetic properties

Single crystals of inorganic–organic hybrid compounds, M₅(OH)₂[CO₂(CH₂)₂CO₂]₄ [M = Mn(Mn-s), Fe(Fe-s), Co(Co-s), Mn/Fe(Mn---Fe-n) and Mn/Co(Mn---Co-n)] were prepared under hydrothermal condition at 180 °C from a mixture of transition metal(II) chlorides, succinic acid, potassium hydroxide, and water. Crystal structure of all compounds present the same structural type in the single-crystal X-ray diffraction refinements and X-ray powder diffraction analysis. The single crystal structural analyses for three homo-metallic compounds were performed and the prepared compounds have divalent metal ions on the basis of bond valence sum calculations. The unit cell constants for the hetero-metallic compounds, e.g., Mn/Fe, Mn/Co solid solutions were determined. Magnetic measurements show that the Mn-s may have antiferromagnetic interaction at low temperature. The Fe-s and the Co-s compounds have ferrimagnetic coupling below 10 K. The Mn---Co-n compounds show the ferromagnetic magnetic behavior while the Mn---Fe-n compounds present antiferromagnetic ordering.     

Aluminum phthalocyanine: an active and simple catalyst for cyanosilylation of aldehydes

Aluminum phthalocyanine (AlPc) in the presence of Ph₃PO acts as a highly effective catalyst for cyanosilylation of various aldehydes to the corresponding cyanohydrin trimethylsilyl ethers. The reaction proceeds smoothly with 5 mol% catalyst loading at room temperature, giving up to 96% yield. Copyright © 2007 John Wiley & Sons, Ltd.     

Some characterizations of Krull domains

In this paper, we define the v-finiteness for a length function L_v on the set of all v-ideals of an integral domain R and show that R is a Krull domain if and only if every proper integral v-ideal of R has v-finite length and L_v((AB)_v)=L_v(A)+L_v(B) for every pair of proper integral v-ideals A and B in R. We also give Euclidean-like characterizations of factorial, Krull, and π-domains. Finally we define the notion of quasi-∗-invertibility and show that if every proper prime t-ideal of an integral domain R is quasi-t-invertible, then R is a Krull domain.     

Low energy electron beam irradiator using sprayed double walled carbon nanotubes

We fabricated a prototype of an e-beam irradiator which is low energy and diode type by using sprayed double walled carbon nanotubes (DWCNTs). The diode type e-beam irradiator consisted of a grounded e-beam window which was made of thin Havar foil and a negatively charged cathode where carbon nanotubes were sprayed on titanium coated aluminum rod. Synthesized DWCNTs which were purified through the chemical processes and then mixed with ethanol were sprayed several hundred times on the surface area of 2×300 mm². A phosphor screen located on the e-beam window and a CCD camera was used to observe the emitted electron beams directly from the cathode to the air with an increase of the voltage. The measured e-beam current was 1.5 mA at −95 kV.     

Synthesis,characterisation, and X-ray structures of zinc(II) complexes bearing camphor-based ethyleneamineimines as pre-catalysts for heterotactic-enriched polylactide from rac-lactide

Transition Metal Chemistry - A series of Zn(II) complexes bearing camphor-based ethyleneamine derivatives, [LnZnCl2]...     

Residual detection of naproxen,methyltestosterone and 17α‐hydroxyprogesterone caproate in aquatic products by simple liquid–liquid extraction method coupled with liquid chromatography–tandem mass spectrometry

In the present study, we aimed to develop a reliable screening method based on liquid chromatography coupled with tandem mass spectrometry (LC–MS/MS) for the detection and quantification of naproxen, methyltestosterone and 17α‐hydroxyprogesterone caproate residues. The target analytes were extracted from samples of eel, flatfish and shrimp using acetonitrile with 1% acetic acid, followed by liquid–liquid purification with n‐hexane. Chromatographic separation was achieved on a reversed‐phase analytical column using 0.1% formic acid containing 10 mm ammonium formate in distilled water (A) and methanol (B) as mobile phases. All the matrix‐matched calibration curves were linear (R² ≥ 0.99) over the concentration range of the tested analytes. Recovery at three spiking levels (0.005, 0.01 and 0.02 mg/kg) ranged from 68 to 117% with intra‐ and inter‐day precisions <10%. Five market samples for each matrix (eel, flatfish and shrimp) were collected and tested for method application. In summary, the proposed method is feasible to screen and quantify the analytes with high selectivity in aquatic food products meant for human consumption.