Exploring network-level performances of wireless nanonetworks utilizing gains of different types of nano-antennas with different materials

Wireless nanonetworks are not a simple extension of traditional communication networks at the nano-scale. Owing to being a completely new communication paradigm, existing research in this field is still at an embryonic stage. Furthermore, most of the existing studies focus on performance enhancement of nanonetworks via designing new channel models and routing protocols. However, the impacts of different types of nano-antennas on the network-level performances of the wireless nanonetworks remain still unexplored in the literature. Therefore, in this paper, we explore the impacts of different well-known types of antennas such as patch, dipole, and loop nano-antennas on the network-level performances of wireless nanonetworks. We also investigate the performances of nanonetworks for different types of traditional materials (e.g., copper) and for nanomaterials (e.g., carbon nanotubes and graphene). We perform rigorous simulation using our customized ns-2 simulation to evaluate the network-level performances of nanonetworks exploiting different types of nano-antennas using different materials. Our evaluation reveals a number of novel findings pertinent to finding an efficient nano-antenna from its several alternatives for enhancing network-level performances of nanonetworks. Our evaluation demonstrates that a dipole nano-antenna using copper material exhibits around 51% better throughput and about 33% better end-to-end delay compared to other alternatives for large-size nanonetworks. Furthermore, our results are expected to exhibit high impacts on the future design of wireless nanonetworks through facilitating the process of finding the suitable type of nano-antenna and suitable material for the nano-antennas.

     

Fluorescence spectroscopy of a naturally occurring carbazole alkaloid: murrayanine

The fluorescence properties of a naturally occurring carbazole alkaloid, murrayanine, have been studied in various polar solvents and micellar systems. It was found that fluorescence peak position and intensity are extremely sensitive to the nature of the solvent medium. Murrayanine fluorescence has been further utilized to determine the critical micellization concentration of Pluronic F68, an amphiphilic copolymer with potential applications in drug-delivery. Time-resolved fluorescence and fluorescence anisotropy decay of murrayanine measured in several n-alcohols display a monotonic retardation with increasing chain-lengths of the alcohols.     

Nickel(II) chloride hexahydrate catalyzed reaction of aromatic aldehydes with 2-mercaptoethanol: formation of supramolecular helical assemblage of the product

Various aromatic aldehydes on reaction with 2-mercaptoethanol provided an unanticipated product, bis(2-hydroxyethyl)dithioacetals (3) as the major product along with the expected product 1,3-oxathiolanes (4) in the presence of 0.05 equiv amount of nickel(II) chloride hexahydrate (NiCl₂·6H₂O) under solvent-free conditions. Products 3c and 3e exhibit an interesting hydrogen-bonded infinite supra-molecular helical structure.     

Coordination complexes of 2‐thienyl‐ and 2‐furyl‐mercurials

The reactions of di(2‐thienyl)mercury, 2‐thienylmercury chloride and 2‐furylmercury chloride with a variety of nitrogen‐ and phosphorus‐containing ligands have been studied. The presence of the electron‐withdrawing heteroatoms results in these mercurials being stronger acceptors than the corresponding phenylmercury compounds. The complexes have been characterized by elemental analysis, melting points, infrared, and ¹⁹⁹Hg NMR spectroscopy. 2,9‐Dimethyl‐ and 3,4,7,8‐tetramethyl‐phenanthroline form 1:1 chelate complexes, as does 1,2‐bis(diphenylphosphino)ethane, whereas ethylenediamine and 2,2′‐bipyridyl do not form complexes. Though non‐chelating ligands such as 2,4′‐ and 4,4′‐bipyridyl do not form complexes, bis(diphenylphosphino)methane forms 1:2 complexes in which the ligand bridges two mercury atoms. Monodentate ligands, such as triphenylphosphine, cause disproportionation of the organomercury chloride. 2‐Thienylmercury chloride forms a 4:1 complex with 4,4′‐dipyridyl disulfide in which it is believed that a molecule of the organomercurial is coordinated to both of the nitrogen and both of the sulfur atoms. Copyright © 2004 John Wiley & Sons, Ltd.     

Biogenic synthesis of Ag, Au and bimetallic Au/Ag alloy nanoparticles using aqueous extract of mahogany (Swietenia mahogani JACQ.) leaves

In this paper, we have demonstrated for the first time, the superb efficiency of aqueous extract of dried leaves of mahogany (Swietenia mahogani JACQ.) in the rapid synthesis of stable monometallic Au and Ag nanoparticles and also Au/Ag bimetallic alloy nanoparticles having spectacular morphologies. Our method was clean, nontoxic and environment friendly. When exposed to aqueous mahogany leaf extract, competitive reduction of Au(III) and Ag(I) ions present simultaneously in same solution leads to the production of bimetallic Au/Ag alloy nanoparticles. UV-visible spectroscopy was used to monitor the kinetics of nanoparticles formation. UV-visible spectroscopic data and TEM images revealed the formation of bimetallic Au/Ag alloy nanoparticles. Mahogany leaf extract contains various polyhydroxy limonoids which are responsible for the reduction of Au(III) and Ag(I) ions leading to the formation and stabilization of Au and Ag nanopaticles.