Modified Eu3+ doped Y2O3 Nanoparticles as Turn-on Fluorescence Sensor for Sensitive Determination of Methamphetamine

Journal of Analytical Chemistry - In this article, a new spectrofluorometric method was developed for the determination of methamphetamine based on a turn-on luminescence response of captopril...     

Hierarchy of rational order families of chaotic maps with an invariant measure

We introduce an interesting hierarchy of rational order chaotic maps that possess an invariant measure. In contrast to the previously introduced hierarchy of chaotic maps [1–5], with merely entropy production, the rational order chaotic maps can simultaneously produce and consume entropy. We compute the Kolmogorov-Sinai entropy of these maps analytically and also their Lyapunov exponent numerically, where the obtained numerical results support the analytical calculations.     

The quantum de Rham complexes associated with SL h (2)

Quantum de Rham complexes on the quantum plane and the quantum group itself are constructed for the nonstandard deformation of Fun(SL(2)). It is shown that in contrast to the standardq-deformation of SL(2), the above complexes are unique for SL _h (2). Also, as a byproduct, a new deformation of the two-dimensional Heisenberg algebra is obtained which can be used to construct models ofh-deformed quantum mechanics.     

Modification of the GV-MSA model in obtaining the activity and osmotic coefficients of aqueous electrolyte solutions

In this work a modified form of the Ghotbi–Vera Mean Spherical Approximation model (MGV-MSA) has been used to correlate the mean ionic activity coefficients (MIAC) for a number of symmetric and asymmetric aqueous electrolyte solutions at 25 °C. In the proposed model the hard sphere as well as the electrostatic contributions to the MIAC and the osmotic coefficient of the previously GV-MSA model has been modified. The results of the proposed model for the MIAC of the electrolyte solutions studied in this work are used to directly calculate the values of the osmotic coefficients without introducing any new adjustable parameter. In the MGV-MSA model the cation diameter as well as the relative permittivity of water depends on the electrolyte concentration. Having considered such dependency for both cation and relative permittivity for water in an electrolyte solution the modification of the GV-MSA has been made. It should be stated that in the MGV-MSA model the anion diameter in the solution similar to that in the GV-MSA model remains constant and independent of the electrolyte concentration. The results obtained from the proposed model have been favorably compared with those of the GV-MSA model. The results showed that the MGV-MSA model can more accurately correlate the MIAC of the single electrolyte solutions than those of the GV-MSA model. The same comparison has been observed in case of the osmotic coefficients for the electrolyte solutions studied in this work. It should be noted that in order to do an unequivocal comparison between the results obtained from the models used in this work the same minimization procedure and the same experimental data for the MIAC and the osmotic coefficients have been used. Also it should be mentioned that in the MGV-MSA model the conversion from the McMillan–Mayer (MM) framework to that of the Lewis–Randall (LR) has been performed. It has been concluded that such transformation can affect the results in particular at higher electrolyte concentrations.     

Adsorptive Behavior of Methylene Blue onto Sawdust of Sour Lemon,Date Palm,and Eucalyptus as Agricultural Wastes

In the present study, to remove methylene blue (MB) from aqueous solution, some agricultural residues and cheap bioadsorbents such as sawdust of palm trees, eucalyptus, and sour lemon were used. To do this, significant parameters like contact time, temperature, pH, initial concentration, and adsorbent dosage were checked. The results affirmed that the best conditions for MB adsorption from aqueous solution were obtained such as the temperature of 25?°C, pH of 8, adsorbent dosage of 2g/L, contact time of 120?minutes, and dye concentration of 5?mg/l which under these conditions the adsorption efficiencies determined were 95.8, 93.4, and 92.8% using sawdust of palm tree, eucalyptus, and sour lemon, respectively. Also, the equilibrium behavior of adsorbents showed that the Freundlich model could better predict the adsorption behavior of the process due to having a larger correlation coefficient (R²). The maximum biosorption capacities by Langmuir isotherm model were also obtained 54, 53.5, and 52.4?mg/g for sawdust of palm trees, eucalyptus, and lemon, respectively, which were significant amounts. In addition, kinetic behavior of adsorption showed that pseudo-second-order model can describe the kinetics of the adsorption process better than the pseudo-first-order model. Moreover, kinetic, equilibrium, and thermodynamic behaviors of adsorption affirmed that the biosorption process was desirable, physisorption, spontaneous, and exothermic.     

Steric selectivity in oxidations of diols

Oxidations of 2,2-disubstituted-1,4-butanediols by the combination of nickel(II) bromide and benzoyl peroxide and by trityl tetrafluoroborate produce β,β-disubstituted-γ-butyrolactones with exceptional selectivity.     

Synthesis,Characterization, and Crystal Structure of Thallium(I) Complex containing Monodeprotonated 2,6‐Pyridinedicarboxylic Acid

The reaction of an ethanolic solution 2,6‐pyridinedicarboxylic acid ( 1 , LH₂) with TlNO₃ in the presence of triethylamine led to the coordination polymer [Tl(LH)]_n ( 2 ). The complex was characterized by elemental analysis, IR spectroscopy and single‐crystal X‐ray diffraction. Crystal data for 2 at –80 °C: monoclinic, space group I2/a, a = 696.1(1), b = 1190.6(2), c = 931.0(2) pm, β = 103.28(1)°, Z = 4, R₁ = 0.0256.     

Rh(II)-Catalyzed Isomerizations of Cyclopropenes Evidence for Rh(II)-Complexed Vinylcarbene Intermediates

The thermocatalytic rearrangements of cyclopropenes 1-4 have been investigated in the presence of Rh(IT) perfiuorobutyrate. 1, 2, 3-Triphenylcyclopropene ( 1a ) undergoes rearrangement lo diphenylindene 5a or, with alkoxycyclopropene derivatives, to α, β-unsaturated ketone 6. Furan formation occurs with 2, 3-diphenylcyclo-propenecarboxylate 2, but the diethyl counterpart 3 rearranges to dienoate 8. 2-Alkylcyclopropenecarboxylates 4 afforded (E)-methylidenecyclopentane derivatives 9 as the only isolable product in yields of ca. 35 %. A mechanism involving regio- and stereospecific cyclopropene ring opening to a Rh-complexed vinylcarbene and insertion of the latter into the C? H bond to give 9 is proposed. An analogous mechanism should account for the rearrangement products of 1 to 3 .     

Synthesis,Characterization and Crystal Structures of new Coordination Polymers of Cerium(III) and Samarium(III) Containing 2,6‐Pyridinedicarboxylic Acid

The reaction of 2,6‐pyridinedicarboxylic acid ( 1 , LH₂) with CeCl₃·7H₂O and Sm(NO₃)₃·6H₂O in the presence of triethylamine led to the coordination polymer complexes [M(L)(LH)(H₂O)₂]·4H₂O [M = Ce ( 2 ) and Sm ( 3 )]. Both complexes were characterized by elemental analyses, IR spectroscopy and the crystal structures of 2 and 3 . Crystal data for 2 at ?80 °C: monoclinic, space group P2₁/c, a = 1404.6(1), b = 1122.1(1), c = 1296.1(1) pm, β = 102.09(1)°, Z = 4, R₁ = 0.0217 and for 3 at ?80 °C: monoclinic, space group P2₁/c, a = 1395.1(1), b = 1120.1(1), c = 1282.8(1) pm, β = 102.71(1)°, Z = 4, R₁ = 0.019.     

HPLC Determination of Letrozole in Plasma Using Fluorescence Detection: Application to Pharmacokinetic Studies

A simple, rapid and sensitive HPLC method has been developed and validated for the analysis of letrozole in human plasma. The separation was achieved on a monolithic silica column using acetonitrile–phosphate buffer. A fluorescence detector was used for the quantitation with excitation and emission wavelengths at 230 and 295 nm. The assay enables the measurement of letrozole for therapeutic drug monitoring with a minimum quantification limit (LOQ) of 0.5 ng mL^?1. The method involves a simple, one-step extraction procedure with complete recovery. Calibration was linear over the concentration range 0.5–80 ng mL^?1. The coefficients of variation for inter-day and intra-day assay were found to be less than 8%.