A note on infinite aS-groups

Let G be a group. If every nontrivial subgroup of G has a proper supplement, then G is called an aS-group. We study some properties of aS-groups. For instance, it is shown that a nilpotent group G is an aS-group if and only if G is a subdirect product of cyclic groups of prime orders. We prove that if G is an aS-group which satisfies the descending chain condition on subgroups, then G is finite. Among other results, we characterize all abelian groups for which every nontrivial quotient group is an aS-group. Finally, it is shown that if G is an aS-group and |G| ≠ pq, p, where p and q are primes, then G has a triple factorization.     

A minimalist NMR approach for the structural revision of mucoxin

In an attempt to revise the structural assignment of mucoxin, and faced with 64 diastereomeric possibilities, we resorted to the synthesis of truncated structures that contained the core stereochemical sites. Twelve stereochemical analogues were synthesized, their (1)H and (13)C NMR spectra were analyzed and four recurring stereochemical trends were distilled from the data. Applying the observed trends to the diastereomeric population pared the possible choices for the correct structure of mucoxin from 64 to 4. Synthesis of these analogues led to the identification of the correct structure of mucoxin.     

Selective oxidation of sulfides to sulfoxides using 30% hydrogen peroxide catalyzed with a recoverable silica-based tungstate interphase catalyst

Various types of aromatic and aliphatic sulfides are selectively oxidized to sulfoxides and sulfones in good to excellent yields using 30% H2O2 in the presence of catalytic amounts of a novel recoverable silica-based tungstate interphase catalyst at room temperature. The catalyst can be recovered and reused for at least eight reaction cycles under the described reaction conditions without considerable loss of reactivity. [reaction: see text]     

Aqueous solutions of ionic liquids: study of the solution/vapor interface using molecular dynamics simulations

We performed a detailed molecular dynamics study of the interfacial structure of aqueous solutions of 1-butyl-3-methylimidazolium tetrafluoroborate in order to explain the anomalous dependence of the surface tension on concentration. At low concentrations the surface tension decreases with concentration. At higher concentrations the surface becomes saturated; a plateau is observed in simulations with a non-polarizable force field while a possible increase is detected in simulations with a polarizable force field. The structure is characterized by a surplus of cations at the surface (with hydrophobic butyl chains pointing toward vacuum) which at low concentrations is only partly compensated by the anions because of asymmetric solvation. A more hydrophobic 1-butyl-3-methylimidazolium hexafluorophosphate is also simulated for comparison.     

A Proline-Based Aminophosphinic Acid Ligand and It’s Vanadyl Complex: Synthesis,Characterization and In Vitro Inhibitory Effects on α-Amylase And α-Glucosidase

Abstract

A proline-based aminophosphinic acid ligand and it's vanadium complex have been synthesized and characterized by spectroscopic techniques. The inhibitory activity on pancreatic α-amylase and Baker's yeast α-glucosidase has been examined in vitro. The novel complex showed more inhibitory potency against pancreatic α-amylase and Baker's yeast α-glucosidase compared to acarbose as an antidiabetic drug.

Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file.     

Defect capture under rapid solidification of the melt induced by the action of femtosecond laser pulses and formation of periodic surface structures on a semiconductor surface

A theory of defect-strain instability with formation of periodic surface relief in semiconductors irradiated by ultra-short (τ_p=10^-13 s) powerful laser pulses is developed. The period and time of formation of surface relief are calculated. Regimes of multi-pulse laser ablation leading to formation of either a smooth surface or arrays of surface-relief spikes are pointed out and corresponding experimental results are interpreted from the viewpoint of the developed theory. Received: 4 December 2000 / Accepted: 23 July 2001 / Published online: 11 February 2002     

Novel method for the synthesis of 1,2,4‐oxadiazoles using alumina supported ammonium fluoride under solvent‐free condition

Alumina supported ammonium fluoride was found as an efficient reagent for the synthesis of 1,2,4‐oxadi‐azoles of amidoximes under solvent free conditions using microwave irradiation. This method is a one‐pot, easy, rapid, and high‐yielding reaction for the synthesis of 1,2,4‐oxadiazole derivatives from amidoximes and acyl chlorides. Reaction of amidoximes with acylchlorides in the presence of alumina without ammonium fluoride gave only the corresponding O‐acylamidoximes as major product.     

Laser‐micromachined cellulose acetate adhesive tape as a low‐cost smart material

An off‐the‐shelf, moisture‐responsive, acetate‐backed adhesive tape is investigated as a commercially available smart material for fabricating low‐cost, multifunctional, humidity‐responsive millimeter‐scale structures. Laser ablation is used for cutting and thinning‐down the tape to enhance its response. Water‐submerged cantilevers show a radius of curvature of 3 mm or lower (for laser‐thinned cantilevers). Additionally, their humidity response is a function of the angle between the longitudinal axis of the cantilever and polymer orientation. A cut angled at 80° with respect to this orientation results in a tip rotation of up to 25°, enabling the formation of bending cantilevers with twisting behavior. The tape cantilevers are further functionalized with magnetic nanoparticles and used to create four‐finger grippers that close underwater within minutes and can sample 100 µL of liquid. A cyclic humidity monitor is also fabricated using a tape strip that walks unidirectionally on a ratchet‐shaped surface upon exposure to humidity variations. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2013 , 51, 1263–1267     

The effect of melt flow index, melt flow rate, and particle size on the thermal degradation of commercial high density polyethylene powder

The powder of EX5 grade of high density polyethylene—without any additives—manufactured by Amirkabir petrochemical company was separated by shaker equipment. The separated powder of average diameter ~25, ~62.5, ~87.5, ~112.5, ~137.5, ~175 and the particles >200 μm was tested by a thermogravimetric (TG) analysis instrument in nitrogen atmosphere and heating rates of 10, 20, and 30 °C min^?1. In addition, the separated powders were analyzed by a melt flow index (MFI) instrument, and the viscosity average molecular mass (M _v) of the powders was tested by a viscometer. Kinetic evaluations were performed by Friedman and Kissinger analysis methods and apparent activation energy for the overall degradation of the powders was determined. The effects of molecular mass, MFI, MFR, and particle size on the degradation TG curve, derivative thermogravimetry curve breadth, and activation energy of thermal degradation were considered. The results showed that the M _v of EX5 pipe grade produced by two serial reactors is increased by increasing of the particle size and, MFI is decreased with a little deviation by particle size increasing. The particle size has no obvious effect on the melt flow rate (MFR), and MFR as function of molecular mass distribution does not change very much. The results showed that the powder with bigger particles and higher molecular mass moderately increases the activation energy and shifts the degradation curve to the higher temperatures.