Structural studies of TcO2 by neutron powder diffraction and first-principles calculations

Crystalline technetium dioxide was prepared and for the first time its crystal structure determined by neutron powder diffraction. In addition, electronic structure calculations using density functional theory were performed to further elucidate the bonding mechanisms in TcO2. The crystal structure determined by Rietveld analysis with the NPD data is of a distorted rutile type, similar to that of MoO2; space group P21/c, a = 5.6891(1), b = 4.7546(1), c = 5.5195(1) A, and beta = 121.453(1) degrees . The NPD analysis also establishes a new neutron scattering length of 6.00(3) fm for 99Tc. Our results clearly show metal-metal bonding between Tc pairs along the edge-sharing chains of TcO6 octahedra. The Tc-Tc bond was found to be 2.622(1) A from NPD profile analysis and 2.59 A from first-principles DFT calculations. The bond is somewhat longer than expected from earlier predictions, suggesting that the nature of the Tc-Tc interaction is weaker than anticipated for the Tc(IV) cation with three outer electrons. The NPD results supported by the DFT calculations suggest that the filling of antibonding orbitals and the influence of the crystal field stabilization of the d3 Tc cations lead to more regular TcO6 octahedra and diminish the metal-metal bond strength compared with closely related oxides such MoO2 and WO2.     

Half-metallicity in graphene nanoribbons with topological defects at edge

We report first principles studies of zigzag edged graphene nanoribbons (ZGNR) with one edge partially covered by topological defects. With increasing coverage of an edge by pentagons and heptagons, which are two of the simplest topological defects possible in a graphenic lattice, ZGNRs evolve from a magnetic semiconductor to a ferromagnetic metal. This evolution can be intermediated by a narrow bandgap half-metallic phase, upon suitable concentration and conformation of defects at the edge. Spin-frustration induced by topological defects lead to substantial lowering of magnetic ordering and localization of defect-states in the vicinity of the defects. Dispersion of bands constituted by the defect-states within the bandgap of the corresponding unmodified ZGNR, leads to availability of energy windows for spin-polarized electron transport. Driven primarily by exchange interactions, the energy window for transport of electrons near Fermi energy, is consistently wider and more prevalent for the minority spin, in the entire class of ZGNRs with discontinuous patches of topological defects at an edge. Such defects have been widely predicted and observed to be naturally present at the interfaces in polycrystalline graphene, and can even be formed through chemical and physical processes. Our approach thus may lead to a feasible strategy to manifest workable half-metallicity in ZGNRs without involving non-carbon dopants or functional groups.     

System dynamic modelling and simulation of hydrodynamic machines

A graph-theoretic framework for the dynamic simulation of hydrodynamic (both axial and radial flow) machines is presented in this article. The physics based analytical models are developed by considering the dynamics of the hydraulic fluid flow and its interaction with the mechanical components. A linear graph is used to capture the topology of the system and the interconnection of the constituent components. Using the graph-theoretic framework, a dynamic model of an automotive hydrodynamic torque converter is developed to simulate its behaviour under different flow conditions. The ability of the model to capture different features of the torque converter will also be demonstrated by simulation. The simulation results are compared with and validated by experimental results in the literature.     

Laser Heated Emissive Probes Design and Development under National Fusion Program and Potential Measurement

Emissive probes are the tools for the direct deter- mination of the plasma potential ~PL and they deliver a more reliable measure of φPL compared to the indi- rect measurements with cold Langmuir probes. The emissive probe works on the principle of compensating the well-known asymmetry of the I-V characteristic of a single cold Langmuir probe by an electron emission current from the probe into the plasma. In an ideal case, the saturated value of floating potential V（А,em） of a highly emissive probe should equal the plasma potential. A conventional emissive probe usu- ally consists of a loop of tungsten wire heated by an electric current passing through it. These conven- tional emissive probes containing an electric current- heated metal wire loop suffer a huge drawback when it comes to their lifetime. The metal wire used in these probes evaporates and subsequently breaks when heated with high current, leading to frequent replacements of these wires. When used in ultra high vacuum （UHV） plasma systems, frequent replacement of these wires requires frequent vacuum breaks in the plasma systems. In many plasma systems espe- cially in magnetized toroidal hot plasmas like toka- maks, where determination of the electric fields leads to a great deal of useful information, frequent breaking of the vacuum is impossible for changing the filament of the emissive probes. Hence, along with the other drawbacks of the conventional emissive probes such as limited emission current, bending in a magnetic field makes their use impractical in these plasma systems. The most suitable alternative is the emissive probes heated by a focused infra-red laser. Due to them having several advantages over the conventional emis- sive probes, laser heated emissive probes （LHEPs） are found to have more and more uses in plasma systems. The advantages of the LHEP are： longer lifetime （no filament breaking issues）, attainment of higher tem- perature without melting or evaporation and thus higher emissivity, no deformation of the pr     

Synthetic Applications of the Baylis–Hillman Reaction: Simple and Convenient Synthesis of Five Important Insect Pheromones

A simple and convenient synthesis of five important insect pheromones by means of Baylis–Hillman adducts is described, i.e., of (2E,4S)‐2,4‐dimethylhex‐2‐enoic acid ( 1 ), a mandibular‐gland secretion of the male carpenter ant in the genus Camponotus, of (+)‐(S)‐manicone ( 2 ) and (+)‐(S)‐normanicone ( 3 ), two mandibular‐gland constituents of Manica ants, and of (+)‐dominicalure‐I ( 6 ) and (+)‐dominicalure‐II ( 7 ), two aggregation pheromones of the lesser grain borer Rhyzopertha dominica (F). For the first time, the potential of the Baylis–Hillman chemistry for the stereoselective synthesis of trisubstituted olefins was successfully applied to the synthesis of these pheromone compounds.     

A facile one-pot stereoselective synthesis of trisubstituted (E)-2-methylalk-2-enoic acids from unactivated Baylis-Hillman adducts and a simple access to some important insect pheromones

An efficient one-pot stereoselective synthesis of trisubstituted (E)-2-methylalk-2-enoic acids has been accomplished by treatment of unactivated Baylis-Hillman adducts, 3-hydroxy-2-methylenealkanoates, with Al-NiCl₂·6H₂O in methanol at room temperature followed by hydrolysis. The method has been applied to the synthesis of three important insect pheromones, (4S,2E)-2,4-dimethyl-2-hexenoic acid, (+)-(S)-manicone and (+)-(S)-normanicone.     

Zinc oxide nanowires in chemical bath on seeded substrates: Role of hexamine

Ceria-doped alumina sol-gel materials were obtained by two synthesis methods at low temperature; using method A, 2-propanol-diluted cerium precursor was slowly added at the time of the aluminum sol formation in acidic environment; using method B, the cerium salt was mixed with the aluminum alkoxide before sol formation in a basic environment. The supports were characterized by N₂ physisorption, thermogravimetric and thermal differential analyses (TGA and DTA), X-ray diffraction (XRD), ²⁷Al Magic Angle Spinning-Nuclear Magnetic Resonance (MAS-NMR), 2-propanol reactions, and ammonia temperature-programmed desorption (NH₃-TPD). The samples obtained by Method B present similar values in properties such as specific areas, pore volumes, pore size distribution, and acidity compared to those of pure alumina; the alumina structure was not modified, but segregated crystallites of CeO₂ were found in samples calcined at 1000 ^∘C, as observed by XRD. The ceria-containing materials synthesized by method A show a thermal behavior similar to that of alumina, with no appreciable segregation of CeO₂ detected by XRD and modifications in the amounts of tetra, penta, and octa-hedral aluminum coordination as determined by NMR. 2-propanol reactions showed a good correlation with acid density determined by NH₃-TPD. As the percentage of ceria in the material increases, surface area, pore volume, and acidity decrease. These changes can be correlated with an increase of pentacoordinated aluminum content. The results indicate that CeO₂ is well dispersed in the alumina framework when method A is used, but synthesis method B does not have the same effect on the CeO₂incorporation.     

Adsorption of 2-aminobenzothiazole on colloidal silver particles: an experimental and theoretical surface-enhanced Raman scattering study

Surface-enhanced Raman scattering (SERS) spectra of the biologically important 2-aminobenzothiazole (2-ABT) molecule adsorbed on silver hydrosols are compared with its FTIR spectrum and normal Raman spectroscopy (NRS) spectrum in the bulk and in solution. The optimized structural parameters and the computed vibrational wavenumbers of the compound have been estimated from ab initio (Hatree-Fock) and density functional calculations. Some vibrational modes of the molecule have been reassigned. Concentration-dependent SERS spectra of the molecule reveal the existence of two types of vertically adsorbed species on colloidal silver particles, whose relative population varies with the adsorbate concentrations. The adsorption geometry and structural parameters of one type of adsorbed species are related to the NRS spectrum of the chemically prepared and theoretically modeled 2-ABT-Ag(I) coordination compound.     

Vibrational dynamics and structural investigation of 2,2'-dipyridylketone using Raman, IR and UV-visible spectroscopy aided by ab initio and density functional theory calculation

Detailed investigation on the vibrational and electronic spectra has been carried out in order to study various properties of 2,2'-dipyridylketone molecule in its ground and excited electronic states. To get insight into the structural and symmetry features of the molecule, Raman excitation profiles of several normal modes have been analyzed. The polarized Raman spectra in different environments along with their IR counterpart have been critically surveyed and different normal modes have been assigned. The knowledge in regard to the positions of different excited electronic states has been acquired from the study of electronic absorption spectra. All the experimental observations have been substantiated and corroborated theoretically by the quantum chemical calculation. Possibility of exciton splitting of the 1La band has been explored both from theoretical and experimental points of view.     

Synthesis and characterization of a novel polyazomethine ether for NLO application

Polymer containing azomethine and ether linking groups between phenylene rings has been prepared. It is a polycondensation reaction of a single monomer containing nitro as well as hydroxyl group in p,p^′ position from 4-nitroaniline and 4-hydroxy benzaldehyde. The polymer has been characterized by elemental analysis, IR, UV and NMR spectroscopies, viscometry and thermal studies. The thermotropic liquid crystalline behaviour of the polymer is investigated by optical polarizing microscopy. The crystalline behaviour of the polymer is confirmed by XRD study. The polymer shows good second harmonic generation for non-linear optical application.