Piecewise linear integrated optical device as an optical isolator using two-port nonlinear ring resonators

A nonlinear (piecewise linear) optical transfer function for optical applications generally and isolator especially is introduced and a realization method for the introduced block based on array of two-port nonlinear ring resonators is proposed. The effect of system parameters on the transfer function is studied. The characteristics of the introduced nonlinear device such as the threshold value and the slope of linear part can be controlled using the coupling coefficients and ring lengths. We show that using our proposed idea, easily more than 30-dB isolation well over 3 THz can be obtained only with similar two rings. Also, insertion loss less than 1 dB can be obtained using optical amplifier between rings. The proposed circuit is compact (0.2 mm²) and easily can be integrated with semiconductor lasers as well as other integrated devices and systems. Finally, the analytical result for approximation of the threshold and slope of linear part is presented.     

Green and mild laccase-catalyzed aerobic oxidative coupling of benzenediol derivatives with various sodium benzenesulfinates

The oxidative coupling reaction between hydroquinone or catechols and various sodium benzenesulfinates was investigated using the laccase from Trametes versicolor, in the presence of O₂ in a phosphate buffer solution at room temperature to afford sulfonyl benzenediols in 75–95% yield.     

New Re(I) tricarbonyl-diimine complexes with N,N′-bis(substituted benzaldehyde)-1,2-diiminoethane Schiff base ligands: Synthesis,spectroscopic and electrochemical studies and crystal structures

The syntheses, structures and spectroscopic properties of tricarbonylrhenium(I) complexes with N,N′-bis(2-bromo, 4-bromo, 4-chloro and 3-methoxybenzaldehyde)-1,2-diiminoethane Schiff base ligands have been investigated in this paper. Characterization of these complexes was carried out with FTIR, NMR, UV–Vis spectroscopy, elemental analysis and X-ray crystallography. The electrochemical behavior of the investigated complexes has been studied by cyclic voltammetry. The crystal structures of the 4-chloro, 4-bromo and 4-methoxy substituted complexes are stabilized by intermolecular C–H?Cl and C–H?O hydrogen bonds. The remarkable features of the 2-bromo, 4-bromo and 4-chloro substituted complexes are short intermolecular halogen–oxygen contacts. In the 4-bromo complex, short intermolecular Br?O and O?O contacts link neighboring molecules along the [1 0 0] direction, which are further stabilized by short intermolecular π?π interactions. In 2-bromo complex, intermolecular Br?O interactions link neighboring molecules into 1D extended chains along the [0 1 0] and [0 0 1] directions, forming a 2D network which is parallel to the bc-plane.     

Analysis of one-dimensional Fibonacci-class quasicrystals using perturbation theory

In this work, we present a new and semi-analytical method to investigate one-dimensional Fibonacci-class photonic quasicrystals from waveguiding properties point of view. Usually, the exact treatment for obtaining band diagram in these situations is very hard and the numerical methods are used. In this paper, we investigate the waveguiding properties of one-dimensional quasicrystals by using perturbation method. In this direction, the band diagram and field distribution of this structure are investigated.     

Numerical solution of stochastic differential equations by second order Runge–Kutta methods

In this paper we propose the numerical solutions of stochastic initial value problems via random Runge–Kutta methods of the second order and mean square convergence of these methods is proved. A random mean value theorem is required and established. The concept of mean square modulus of continuity is also introduced. Expectation and variance of the approximating process are computed. Numerical examples show that the approximate solutions have a good degree of accuracy.     

Hydrophilic alginate based multidentate biopolymers for surface modification of CdS quantum dots

We report that sodium alginate and its graft-copolymers with (2-dimethylaminoethyl) methacrylate may attach to the surface of colloidal CdS-thioglycerol quantum dots (QDs) via a ligand exchange process and result in water-soluble and highly stable QD supramolecules. Optical properties of modified QDs in water showed that the emission intensity of QDs was still high after surface passivation.     

[C6(MIm)2]2W10O32. 2H2O: A novel and powerful catalyst for the synthesis of 4-arylidene-2-phenyl-5(4)-oxazolones under ultrasonic condition

Di[1,6-bis(3-methylimidazolium-1-yl)hexane] decatungstate dihydrate ([C₆(MIm)₂]₂W₁₀O₃₂. 2H₂O) as a new family of polyoxometalate-based dicationic ionic liquids (POM-DIL) is synthesized and employed as a novel and powerful heterogeneous catalyst in the synthesis of 4-arylidene-2-phenyl-5(4)-oxazolones (azlactones) under ultrasound-assisted solvent-free condition. On the basis of the results, the products were obtained in excellent yields under mild condition. Utilization of easy work-up and purification make it very interesting from an economic perspective. Moreover, a recycling study confirmed that the catalyst can be reused multiple times without significant loss of its activity.     

Statistically disordered short hydrogen bonds in (pipzH2)(cdoH)2 and a comparison with (pipzH2)(cdo)·H2O (pipz is piperazine and cdoH2 is chelidonic acid)

Two related proton‐transfer compounds, namely piperazine‐1,4‐diium 4‐oxo‐4H‐pyran‐2,6‐dicarboxylate monohydrate, C₄H₁₂N₂²⁺·C₇H₂O₆²⁻·H₂O or (pipzH₂)(cdo)·H₂O, (I), and piperazine‐1,4‐diium bis(6‐carboxy‐4‐oxo‐4H‐pyran‐2‐carboxylate), C₄H₁₂N₂²⁺·2C₇H₃O₆⁻ or (pipzH₂)(cdoH)₂, (II), were obtained by the reaction of 4‐oxo‐4H‐pyran‐2,6‐dicarboxylic acid (chelidonic acid, cdoH₂) and piperazine (pipz). In (I), both carboxyl H atoms of chelidonic acid have been transferred to piperazine to form the piperazine‐1,4‐diium ion. The structure is a monohydrate. All potential N—H donors are involved in N—H...O hydrogen bonds. The water molecule spans two anions via the 4‐oxo group of the pyranose ring and a carboxylate O atom. The hydrogen‐bonding motif is essentially two‐dimensional. The structure is a pseudomerohedral twin. In the asymmetric unit of (II), the anion consists of monodeprotonated chelidonic acid, while the piperazine‐1,4‐diium cation is located on an inversion centre. The single carboxyl H atom is disordered in two respects. Firstly, the disordered H atom is shared equally by both carboxylic acid groups. Secondly, the H atom is statistically disordered between two positions on either side of a centre of symmetry and is engaged in a very short hydrogen‐bonding interaction; the relevant O...O distances are 2.4549 (11) and 2.4395 (11) Å, and the O—H...O angles are 177 (6) and 177 (5)°, respectively. Further hydrogen bonding of the type N—H...O places the (pipzH₂)²⁺ cations in pockets formed by the chains of (cdoH)⁻ anions. In contrast with (I), the (pipzH₂)²⁺ cations form hydrogen‐bonding arrays that are perpendicular to the anions, yielding a three‐dimensional hydrogen‐bonding motif. The structures of both (I) and (II) also feature π–π stacking interactions between aromatic rings.