Multi-spectral antireflection coating on zinc sulphide simultaneously effective in visible,eye safe laser wave length and MWIR region

In recent years multi-spectral device is steadily growing popularity. Multi-spectral antireflection coating effective in visible region for sighting system, laser wavelength for ranging and MWIR region for thermal system can use common objective/receiver optics highly useful for state of art thermal instrumentation. In this paper, design and fabrication of antireflection coating simultaneously effective in visible region (450–650 nm), Eye safe laser wave length (1540 nm) and MWIR region (3.6–4.9 μm) has been reported. Comprehensive search method of design was used and the number of layers in the design was optimised with lowest evaluated merit function studied with respect to various layers. Finally eight-layer design stack was established using hafnium oxide as high index layer and silicon-di-oxide as low index coating material combination. The multilayer stack had been fabricated by using electron beam gun evaporation system in Symphony 9 vacuum coating unit. During layer deposition the substrate was irradiated with End-Hall ion gun. The evaporation was carried out in presence of oxygen and layer thicknesses were measured with crystal monitor. The result achieved for the antireflection coating was 85% average transmission from 450 to 650 nm in visible region, 95% transmission at 1540 nm and 96% average transmission from 3.6 to 4.9 μm in MWIR region.     

Supramolecular carbohydrate scaffold-catalyzed synthesis of tetrahydroquinolines

Natural supramolecular carbohydrate scaffold-catalyzed synthesis of tetrahydroquinoline derivatives by the reaction of aromatic amine and cyclic enol ether in excellent yield with high diastereoselectivity has been developed. Carbohydrates, cellulose, and starch were converted into their sulfonic acid derivative and these scaffolds exhibit efficient catalytic properties, along with excellent cost effectivity and recyclability.     

Rheology-modulated alterations in electro-magneto-hydrodynamic flows in a narrow cylindrical capillary: Contrasting trends in high and low surface charge limits

We investigate electrokinetic transport of power-law fluids in a narrow cylindrical capillary in the presence of a transverse magnetic field. The governing equations including the full Poisson-Boltzmann equation and the Cauchy momentum equation with power-law constitutive behavior are solved numerically, without being restrictive to low surface potential limits. The influence of the power-law index, wall zeta potential, relative strength of electromagnetic force over viscous force (as represented by the Hartmann number), and the lateral electric field strength on the variation of the volumetric flow rate is analyzed. Our results reveal a significant augmentation in the net-throughput beyond the traditionally explored low surface-charge limits, especially for shear-thinning fluids, defying the established notions. These fundamental theoretical premises may act as essential precursors towards developing deeper insights on fluidic transport bio-nanopores under electro-magneto- hydrodynamic influences.     

Identification of α- and β-hydroxy acid containing cyclodepsipeptides in natural peptide mixtures using negative ion mass spectrometry

Natural peptide libraries often contain cyclodepsipeptides containing α- or β-hydroxy residues. Extracts of fungal hyphae of Isaria yield a microheterogenous cyclodepsipeptide mixture in which two classes of molecules can be identified by mass spectral fragmentation of negative ions. In the case of isaridins, which contain an α-hydroxy residue and a β-amino acid residue, a characteristic product ion corresponding to a neutral loss of 72 Da is obtained. In addition, neutral loss of water followed by a 72 Da loss is also observed. Two distinct modes of fragmentation rationalize the observed product ion distribution. The neutral loss of 72 Da has also been obtained for a roseotoxin component, which is also an α-hydroxy residue containing cyclodepsipeptide. In the case of isariins, which contain a β-hydroxy acid residue, ring opening and subsequent loss of the terminal residue as an unsaturated ketene fragment, rationalizes the observed product ion formation. Fragmentation of negative ions provide characteristic neutral losses, which are diagnostic of the presence of α-hydroxy or β-hydroxy residues.     

Monitoring the dynamics of ligand-receptor complexes on model membranes

Ligand-induced cross-linking of cell surface receptors is a basic paradigm of signal activation by many transmembrane receptors. After ligand binding, the receptor complexes formed on the membrane are dynamically maintained by two-dimensional protein-protein interactions on the membrane. The biophysical principles governing the dynamics of such interactions have not been understood, mainly because the measurement of lateral interactions on membranes so far has not been experimentally addressed. Here, we describe a generic approach for measuring two-dimensional dissociation rate constants in vitro using a novel high-affinity chelator lipid for reconstituting a ternary cytokine-receptor complex on solid-supported membranes. While monitoring the interaction between the ligand and one of the receptor subunits on the membrane by fluorescence resonance energy transfer, the equilibrium on the surface was perturbed by rapidly tethering a large excess of the unlabeled receptor subunit. Displacement of labeled by unlabeled protein in the ternary complex was detected as a recovery of the donor quenching. Since the dissociation of the ligand-receptor complex in plane of the membrane was the rate-limiting step under these conditions, the two-dimensional rate constant of this process was determined. Strikingly, the two-dimensional dissociation was much slower than ligand dissociation into solution, suggesting that membrane tethering significantly affects the dissociation process. This result highlights the importance of studying ligand-receptor complexes tethered to membranes for understanding the principles governing signal activation by ligand-induced receptor assembling.     

Hydrogen bonding in phosphonate cavitands: Investigation of host-guest complexes with ammonium salts

The H-bonding in alkylammonium complexes of phosphonate cavitands were studied by mass spectrometric methods and theoretical calculations. The alkylammonium ions included primary, secondary, and tertiary methyl- and ethylammonium ions. Their complexation with mono-, tetra-, and two di-phosphonate cavitands, which differ according to the number and position of H-bond acceptor P = O groups, was evaluated by using different competition experiments, energy-resolved CID, gas-phase H/D-exchange, and ligand-exchange reactions, together with ab initio theoretical optimization of the complexes. The phosphonate cavitands with two or more adjacent P = O groups were found to be selective towards secondary alkylammonium ions, due to simultaneous formation of two stable hydrogen bonds. In the ion-molecule reactions (both H/D- and ligand-exchange), the formation of two stable hydrogen bonds was observed either to slow down the reaction or to completely prevent it. This was, however, limited to situations where two hydrogen bonds are formed between the H-bond donor sites of the alkyl ammonium ion and the vicinal H-bond acceptor sites of the cavitand.     

Polycondensation of benzyl chloride over Ga- and In-modified ZSM-5 type zeolites and Si-MCM-41 or Montmorillonite-K10 supported GaCl3 and InCl3 catalysts

Performance of In- and Ga-modified ZSM-5 type zeolites (namely, In₂O₃/H-ZSM-5, Ga₂O₃/H-ZSM-5, H-GaMFI and H-GaAlMFI) and InCl₃ or GaCl₃ supported on high silica mesoporous MCM-41 or on Mont.-K10 in the liquid phase polycondensation of benzyl chloride to polybenzyl has been investigated. Influence of solvent (namely, dichloroethane, n-heptane and ethanol) and temperature on the rate of polycondensation of benzyl chloride over the catalyst (InCl₃/Si-MCM-41) showing highest polycondensation activity has also been studied. The In- and Ga-containing solid catalysts show good or high activity in the polycondensation reaction at the reaction condition normally employed in the benzylation of aromatic compounds by benzyl chloride. However, the polycondensation is strongly influenced by the solubility of the polybenzyl polymer in the reaction medium and consequently by the solvent used as the reaction medium.