A New Polymer of Mixed‐Anions Complex [Pb(phen)(O2CCH3)(O2NO)]n (phen = 1,10‐phenanthroline)

The single crystal X‐ray data of a mixed anions complex of Pb^II with 1,10‐Phenantroline, [Pb(phen)(O₂CCH₃)‐ (O₂NO)], shows the complex to be polymeric as a result of acetate ligand bridging. The Pb atom has an asymmetrical eightfold coordination of two nitrogen atoms of the 1,10‐phenanthroline ligand and six oxygen atoms of the nitrate and acetate anions. The arrangement of the 1,10‐phenantroline ligand, acetate and nitrate anions suggest a gap in the coordination around the Pb^II ion, occupied possibly by a stereoactive lone pair of electrons on lead(II) where the coordination around the lead atoms is hemidirected. There is a π‐π stacking interaction between the parallel aromatic rings of an adjacent chain in the compound which might help to increase the ‘gap' in the coordination around the Pb^II ion.     

A comparative study on various spectrometries with thin layer chromatography for simultaneous analysis of drotaverine and nifuroxazide in capsules

Three spectrophotometric methods including Vierordt's method, derivative, ratio spectra derivative, and thin layer chromatography (TLC)-UV densitometric method were developed for simultaneous determination of drotaverine HCl (DRT) and nifuroxazide (NIF) in presence of its impurity, 4-hydroxybenzohydrazide (4-HBH). In Vierordt's method, (E(1 cm)(1%)) values were calculated at 227 and 368 nm in the zero-order spectra of DRT and NIF. By derivative spectrophotometry, the zero-crossing method, drotaverine HCl was determined using the second derivative at 245 nm and the third derivative at 238 nm, while nifuroxazide was determined using the first derivative at 399 nm and the second derivative at 411 nm. The ratio spectra derivative spectrophotometry is basedon the measure of the amplitude at 459 nm for DRT and at 416 nm for NIF in the first derivative of the ratio spectra. Calibration graphs of the three spectrophotometric methods were plotted in the range 1-10 mug/ml of DRT and 2-20 mug/ml of NIF. TLC-UV densitometric method was achieved on silica gel plates using ethyl acetate : methanol : ammonia 33% (10 : 1 : 0.1 v/v/v) as the mobile phase. The Rf values were 0.74, 0.50, 0.30+/-0.01 for DRT, NIF and 4-HBH, respectively. On the fluorescent plates, the spots were located by fluorescence quenching and the densitometrical area were measured at 308 and 287 nm with linear range 0.2-4 mug/spot and 0.6-12 mug/spot for DRT and NIF, respectively. The proposed methods have been successfully applied to the commercial pharmaceutical formulation without any interference of excipients. Mean recoveries, relative standard deviations and the results of the proposed methods were compared with those obtained by applying the alternate methods.     

Pulsed Nd:YAG passive Q-switched laser using Cr4+:YAG crystal

In this paper, we report the experimental results of a pulsed flash lamp Nd:YAG laser at wavelength of 1064 nm and Q-switched by Cr⁴⁺:YAG solid state saturable absorber. We have obtained the output energy (E) and pulse- width (τ_p) of this laser for various initial transmissions of this saturable absorber. Furthermore, the effect of reflectivity of the output coupler (R), diameter of the rod (d), and optical length of the cavity (l) on this laser output data have been investigated. We have used the corner cube as a back mirror, which shows high laser stability and better brightness. We have obtained pulse-width 15 ns with 31 mJ output energy. We have also analyzed this laser theoretically and analytically, which agrees well with our corresponding experimental results.     

[Pb2(AMP)2(μ‐X)2X2], X = Br− and I−, AMP = 2‐aminomethylpyridine,Two New Dimeric Lead(II) Complexes Extended in One‐dimensional Helical Chain Polymers by Noncovalent π–π‐stacking

The two lead(II) complexes [Pb₂(AMP)₂(μ‐X)₂X₂], X = Br^?, I^? and AMP = 2‐aminomethylpyridine, have been synthesized and characterized. Self‐assembly of these compounds in the solid state via π–π‐stacking interactions is discussed.     

Modeling the capability of penetrating a jammed crowd to eliminate freezing transition

Frozen state from jammed state is one of the most interesting aspects produced when simulating the multidirectional pedestrian flow of high density crowds. Cases of real life situations for such a phenomenon are not exhaustively treated.Our observations in the Hajj crowd show that freezing transition does not occur very often. On the contrary, penetrating a jammed crowd is a common aspect. We believe the kindness of pedestrians facing others whose walking is blocked is a main factor in eliminating the frozen state as well as in relieving the jammed state. We refine the social force model by incorporating a new social force to enable the simulated pedestrians to mimic the real behavior observed in the Hajj area.Simulations are performed to validate the work qualitatively.     

Zinc(II), Cadmium(II), and Mercury(II) Complexes with the 2, 2′‐Diamino‐4, 4′‐bithiazole (DABTZ) Ligand — Syntheses and X‐Ray Crystal Structure of [Hg(DABTZ)(SCN)2]

Reaction of the ligand 2, 2′‐diamino‐4, 4′‐bithiazole (DABTZ) with Zn(ClO₄)₂, CdCl₂, and Hg(SCN)₂ gives complexes with composition [Zn(DABTZ)₂](ClO₄)₂, [Cd(DABTZ)₂Cl₂], and [Hg(DABTZ)(SCN)₂]. The complexes were characterized by elemental analyses and infrared spectroscopy. The crystal structure of the [Hg(DABTZ)(SCN)₂] was determined by X‐ray crystallography. The complex is built up of a monomeric Hg(SCN)₂ unit with one 2, 2′‐diamino‐4, 4′‐bithiazole ligand coordinated to the Hg atom via the two N atoms giving rise to a five‐member chelate ring in a distorted tetrahedral environment. There is π‐π stacking interaction between the parallel aromatic rings belonging to adjacent chain as planar species in which the mean molecular planes are close to parallel and separated by a distance of ～ 3.5Å, close to that of the planes in graphite. The coordinated 2, 2′‐diamino‐4, 4′‐bithiazole molecule is involved in hydrogen bonding acting as hydrogen‐bond donors with N atoms from the SCN ligand as potential hydrogen‐bond acceptors. The hydrogen bonding yields infinite chains parallel to the crystallographic vectors a and b. Each molecule is bonded to three neighbours. Both amine H atoms are hydrogen bonded to N atoms.