Superperiodicity,chaos and coexisting orbits of ion-acoustic waves in a four-component nonextensive plasma

Superperiodicity, chaos and coexisting orbits of ion-acoustic waves (IAWs) are studied in a multi-component plasma consisting of fluid ions, q -nonextensive cold and hot electrons and Maxwellian hot positrons. The significant impacts of the system parameters on superperiodic and nonlinear periodic IAWs are presented. Considering an external periodic perturbation various types of quasiperiodic and chaotic features for IAWs are studied in different parametric ranges through time series’ plots, phase spaces and Lyapunov exponents. It has been observed that there exist some coexisting orbits for IAWs. Coexisting orbits for IAWs in a classical electron–positron–ion plasma system are reported.     

Advantage of Quantum Theory over Nonclassical Models of Communication

Quantum correlations provide dramatic advantage over the corresponding classical resources in several communication tasks. However, a broad class of probabilistic theories exists that attributes greater success than quantum theory in many of these tasks by allowing supra-quantum correlations in “space-like” and/or “time-like” paradigms. In this letter, a communication task involving three spatially separated parties is proposed where one party (verifier) aims to verify whether the bit strings possessed by the other two parties (terminals) are equal or not. This task is called authentication with limited communication, the restrictions on communication being: i) the terminals cannot communicate with each other, but (ii) each of them can communicate with the verifier through single use of channels with limited capacity. Manifestly, classical resources are not sufficient for perfect success of this task. Moreover, it is also not possible to perform this task with certainty in several nonclassical theories although they might possess stronger “space-like” and/or “time-like” correlations. Surprisingly, quantum resources can achieve the perfect winning strategy. The proposed task thus stands apart from all previously known communication tasks as it exhibits quantum advantage over other nonclassical strategies.     

A terahertz polarization insensitive dual band metamaterial absorber

Metamaterial absorbers have attracted considerable attention for applications in the terahertz range. In this Letter, we report the design, fabrication, and characterization of a terahertz dual band metamaterial absorber that shows two distinct absorption peaks with high absorption. By manipulating the periodic patterned structures as well as the dielectric layer thickness of the metal-dielectric-metal structure, significantly high absorption can be obtained at specific resonance frequencies. Finite-difference time-domain modeling is used to design the structure of the absorber. The fabricated devices have been characterized using a Fourier transform IR spectrometer. The experimental results show two distinct absorption peaks at 2.7 and 5.2?THz, which are in good agreement with the simulation. The absorption magnitudes at 2.7 and 5.2?THz are 0.68 and 0.74, respectively.     

Antioxidant Cardioprotection against Reperfusion Injury: Potential Therapeutic Roles of Resveratrol and Quercetin

Ischemia-reperfusion myocardial damage is a paradoxical tissue injury occurring during percutaneous coronary intervention (PCI) in acute myocardial infarction (AMI) patients. Although this damage could account for up to 50% of the final infarct size, there has been no available pharmacological treatment until now. Oxidative stress contributes to the underlying production mechanism, exerting the most marked injury during the early onset of reperfusion. So far, antioxidants have been shown to protect the AMI patients undergoing PCI to mitigate these detrimental effects; however, no clinical trials to date have shown any significant infarct size reduction. Therefore, it is worthwhile to consider multitarget antioxidant therapies targeting multifactorial AMI. Indeed, this clinical setting involves injurious effects derived from oxygen deprivation, intracellular pH changes and increased concentration of cytosolic Ca²⁺ and reactive oxygen species, among others. Thus, we will review a brief overview of the pathological cascades involved in ischemia-reperfusion injury and the potential therapeutic effects based on preclinical studies involving a combination of antioxidants, with particular reference to resveratrol and quercetin, which could contribute to cardioprotection against ischemia-reperfusion injury in myocardial tissue. We will also highlight the upcoming perspectives of these antioxidants for designing future studies.     

Fermented Baker's Yeast: An Efficient Catalyst for the Synthesis of Pyran Derivatives in Water at Room Temperature

An environmentally friendly, one-pot synthesis of biologically important pyran derivatives in water is described herein. The advantages of this method are its simplicity, cost-effectiveness, and environmental friendliness. Water was exploited both as reaction media as well as activator of catalyst (fermentation of bakers' yeast). Compared with other methods for synthesis of pyran derivatives, satisfactory results were obtained with good yields under simple experimental procedure.     

Effect of denaturation of DNA on the molecular organization of a fluorescent dye in ultra thin films

Acridine Orange (AO) forms H-dimer in solid state and in ultra thin films. However, H dimer of AO reduces its efficiency as a usefull material for fluorescence probe. In the present work detailed investigations has been done on the interaction of AO with different forms of DNA in order to check the effectiveness in controlling the dimeric sites of AO in the Layer by Layer (LbL) self assembled film. It was found that single stranded DNA (ssDNA) is most effective than the dsDNA and coil-shaped DNA in controlling the dimeric sites of AO in LbL film.     

Chromium complexes of an isomeric N-donor ligand, 2-[(N-arylamino)phenylazo]pyridine: amination reactions,X-ray structure,and redox properties

The chromium chemistry of two positional isomers of the ligand 2-[(N-arylamino)phenylazo]pyridine (HL(1)and HL(2)) are described. While the ligand HL(1) coordinates as a bischelating tridentate N,N,N-donor, [L(1)](-), with deprotonation of the amine nitrogen, its isomer HL(2) coordinates as a neutral bidentate N,N-donor. The amine nitrogen in this case remains protonated. Thus the reaction of CrCl(3).nH(2)O with HL(1) produced the brown cationic complex, [Cr(L(1))(2)](+), [1](+). The representative X-ray structure of [1a](ClO(4)) is reported. The two azo nitrogens of the anioinc tridentate ligand approach the metal center closest with Cr(1)-N(azo) av 1.862(6) A. There is a significant degree of ligand backbone conjugation in the coordinated ligands, which resulted in shortening of the C-N distances and also in lengthening of the diazo (N=N) distances. Two synthetic approaches for the synthesis of chromium complexes of HL(2) are investigated. The first approach is based on the substitution reaction, wherein all the coordinated CO ligands of Cr(CO)(6) were completely substituted by the three bidentate HL(2) ligands to produce a violet complex [Cr(HL(2))(3)]. The second approach is based on para-amination reaction of coordinated 2-(phenylazo)pyridine (pap). Thus the reaction of an inert complex, [CrCl(2)(pap)(2)], with ArNH(2) yields a mixed ligand complex, [CrCl(2)(pap)(HL(2))], 3. In this reaction one of the two coordinated pap ligands in [CrCl(2)(pap)(2)] undergoes amination at the para carbon (with respect to the diazo function) to yield HL(2) in situ. This metal-promoted transformation is authenticated by the X-ray structure determination of a representative complex, [CrCl(2)(pap)(HL(2a))], 3a. Notable differences in bond distances along the ligand backbones of the two coordinated ligands in 3a indicate different levels of metal-ligand overlap in this complex. All the chromium complexes of HL(2) are characterized by their intense blue-violet color. The frequencies of the visible range transitions in these complexes linearly correlate with the Hammett's substitution constant. Intraligand charge-transfer transitions in the visible region are believed to be responsible for the intense color. Redox properties of all these complexes are reported.