Surface modification of glassy carbon electrode with the functionalized carbon nanotube for ultrasensitive electrochemical detection of risperidone

Risperidone (RIS), one of the typical antipsychotics drugs, originally approved to be used for the mental illness treatment, especially schizophrenia, bipolar disorder, autism and major depression. In the present study, different carbon nanostructures including functionalized multi-walled carbon nanotubes (F-MWCNTs), carbon nanoparticles, nanodiamond-graphite and reduced graphene oxide were employed for modification of the surface of glassy carbon electrode (GCE) for ultrasensitive detection of RIS. The most significant increase in the anodic peak current of RIS was observed on F-MWCNTs-modified electrode (compared to the other modified electrodes and bare GCE). The influence of different experimental parameters such as pH of the buffered solutions, the amount of the modifier and time and potential of the accumulation was optimized by monitoring the LSV responses toward RIS for the selected modified electrode. A wide linear dynamic range of 0.04–7 µM with a low detection limit of 12 nM was obtained. The results exhibit an acceptable performance of the proposed electrode for determination of RIS in the pharmaceutical and clinical preparations.     

Oxatriquinane and oxatriquinacene: extraordinary oxonium ions

Oxatriquinane, a fused, tricyclic alkyl oxonium ion of unprecented stability, was synthesized in five steps from 1,4,7-cyclononatriene. It survives reflux in H2O, chromatography, and attack by alcohols, alkyl thiols, halide ions, and hindered amine bases. The X-ray crystal structure shows longer C-O bond distances and more acute C-O-C bond angles than any reported alkyloxonium salt. The corresponding oxatriquinene and oxatriquinacene were also synthesized and represent the first examples of stable allyl oxonium species.     

Selective ion-imprinted polymers for preconcentration and determination of silver in water and hair by electrothermal atomic absorption spectrometry

A new Ag(I)-ion imprinted polymer (IIP) was prepared by formation of 2-(4-hydroxypent-3-en-2-ylideneamine) phenol complex for selective extraction and preconcentration of silver ions. Polymerization was performed with ethylene glycol dimethacrylate as crosslinking monomer and methacrylic acid as functional monomer in the presence of 2,2-azobis(isobutyronitrile) as initiator via bulk polymerization method. The Ag(I)-imprinted polymeric particles were characterized by scanning electron microscopy and infrared spectroscopy. The template silver ion was removed from the polymeric matrix using 2.0 M HNO₃. Optimum pH for maximum sorption was 6.0. Maximum sorbent capacity and enrichment factor for Ag(I) were 12.5 mg/g and 50, respectively. The relative standard deviation and detection limit of the method were evaluated as ±4% and 2.3 ng/L, respectively. The developed IIP has also been tested for preconcentration and recovery of Ag(I) ions from water and hair samples.     

Kaplansky Classes and Cotorsion Theories of Complexes

In this article we provide arguments for constructing Kaplansky classes in the category of complexes out of a Kaplansky class of modules. This leads to several complete cotorsion theories in such categories. Our method gives a unified proof for most of the known cotorsion theories in the category of complexes and can be applied to the category of quasi-coherent sheaves over a scheme as well as the category of the representations of a quiver.     

Computational modelling of fluid structure interaction at nano-scale boundaries with modified Maxwellian velocity distribution

The soft collisions among fluid–fluid and fluid-wall molecules are modeled from first principles. In particular, the assumption of Maxwellian distribution of velocities for thermalized molecules, in both parallel and perpendicular directions to the wall, has been re-evaluated with supporting experimental and/or numerical evidence.It is proposed that the normal component of molecular velocity post collision is conserved for all fluid molecules. The slip effect at the wall boundary, introduced by the surface roughness, is accounted by an accommodation coefficient f. A moving least square method is used to calculate macroscopic velocity values. The influence of molecular interaction on the macroscopic velocity distribution is investigated at 40 MPa and 300 K for slit pore, inclined and stepped wall configurations. The accommodation coefficient values f = 0, 0.07, 0.257, 0.45, 0.681 and 1; and acceleration values ranging from zero to 1 × 10¹¹ m/s² and 250 × 10¹¹ m/s² are used for comparison.The distribution of macroscopic velocity parallel to the wall is studied to observe the effect of the slip behaviour. The detailed study of average of velocity values at various magnitudes of acceleration has shown an evidence of characteristic low and high speed of molecular flows that is considered as significant and a comparison is sought with an equivalent laminar and turbulent flow style behaviour. The two dimensional vector and contour plots of macroscopic velocity provide further insights in understanding Continuum velocity distributions resulting from molecular fluid-wall interaction at nanoscale. The research has highlighted the need to develop molecular dynamics simulation techniques for non-periodic boundary conditions.     

The R3O+···H+ hydrogen bond: toward a tetracoordinate oxadionium(2+) ion

Oxatriquinanes are tricyclic oxonium ions which are known to possess remarkable solvolytic stability compared to simple alkyl oxonium salts. Their rigid, hemispherical structure presents an oxygen at the apex of three fused five-membered rings. While trivalent oxygen species like these have been well described in the literature, the ability of oxygen to enter into a fourth covalent bonding relationship has been visited in theory and suggested by the outcome of certain reactions conducted in superacidic media, but has never been established by the characterization of a stable, persistent R(3)OH(2+) or R(4)O(2+) ion. In this study, the nucleophilicity of the oxatriquinane oxygen was evaluated first by a series of protonation studies using the Br?nsted superacid H(CHB(11)Cl(11)) both in the solid state and in liquid HCl solution. The interaction of the oxatriquinane oxygen with a bridging carbocation was also examined. A strong case could be made for the occurrence of hydrogen bonding between H(CHB(11)Cl(11)) and oxatriquinane using IR spectroscopy. Under the most forcing protonation conditions, the oxatriquinane ring is cleaved to give a bridged, dicationic, protonated tetrahydrofuran-carbenium ion.     

Application of Mie theory and fractal models to determine the optical and surface roughness of Ag–Cu thin films

Thin films of Ag/Cu were deposited by reactive DC magnetron sputtering on (001)-oriented Si and glass substrates for various deposition times (4–24 min). These films were characterized by atomic force microscopy (AFM), and a power law scaling was performed on the obtained micrographs to investigate the self-affine nature of the sample morphology, which is indicative of a fractal structure. We applied the Higuchi’s algorithm to the AFM data to determine the fractal dimension of each sample, and the Hurst exponents were computed. The deposition time dependences of these parameters and the grain size distributions estimated from the UV–visible spectra using the Mie theory, allowed us to describe a particle formation mechanism during the deposition process, in which the length of continuous paths of conductive particles increases as the deposition time is increased. In agreement with this explanation, the electrical resistance decreased with the increment of the deposition time.     

Optical bistability at low light level due to collective atomic recoil

We demonstrate optical nonlinearities due to the interaction of weak optical fields with the collective motion of a strongly dispersive ultracold gas. The combination of a recoil-induced resonance in the high gain regime and optical waveguiding within the dispersive medium enables us to achieve a collective atomic cooperativity of 275+/-50 even in the absence of a cavity. As a result, we observe optical bistability at input powers as low as 20 pW. The present scheme allows for dynamic optical control of the dispersive properties of the ultracold gas using very weak pulses of light. The experimental observations are in good agreement with a theoretical model.