Kinetics and Mechanism of the Reaction of Triphenylphosphine with Methyl Vinyl Ketone

Russian Journal of General Chemistry - Kinetics of the reaction of triphenylphosphine with methyl vinyl ketone has been studied using the stopped flow technique. The experimental data have...     

Spectroscopy of Zinc Oxide Thin Films near the Fundamental Absorption Edge

Optics and Spectroscopy - The optical absorption spectra of zinc oxide (ZnO) thin films formed by reactive cathode sputtering are studied. The observed absorption of light in the region of photon...     

Experimental and numerical analysis of cylindrical turbulators in a double pipe heat exchanger under turbulent flow conditions

In the present work, the use of cylindrical turbulators in a double pipe heat exchanger has been investigated. Cylindrical fin type of turbulators has been placed circumferentially separated by 90° on the outer side of an inner pipe at a regular pitch. Experimental studies were undertaken for different air flow rates in a turbulent regime whose Reynolds number range between 2500 and 10000. Heat transfer characteristics like Nu and friction factor have been experimentally determined. Parametric studies were conducted by changing the pitch and also the orientation of the turbulators. Nu and friction factor were found to increase as the pitch is reduced. A model with alternatively changed orientation outperformed others by exhibiting highest Nu and reduced friction factor.     

Theoretical and experimental studies on optically tunable hydrogen bonded liquid crystal complex derived from mesogenic and non-mesogenic aromatic compound

A novel hydrogen bonded liquid crystal (HBLC) complex is synthesized from non-mesogenic benzylmalonic acid (BMA) and mesogenic 4-nonyloxybenzoic acid (9OBA). Structural properties and optimized vibrational frequencies of BMA + 9OBA have been studied by FT-IR spectrum. The weak intermolecular interaction between the molecules is proved by NBO and Mulliken charge distribution analysis. The optical and thermal properties are investigated by POM, DSC, UV-Visible and PL techniques. The present HBLC complex exhibits schlieren textures of nematic, broken focal conic texture of smectic C and multicolored mosaic texture of smectic G phases respectively which is not observed in the pure mesogen (9OBA). The HBLC complex geometry is optimized by DFT method at the level of B3LYP basis set 6311G (d, p). The electronic properties of HBLC complex such as, NBO, HOMO-LUMO, ESP and Mulliken charge distribution are also studied. A noteworthy observation is brought out by identifying the presence of photoluminescence in nematic phase due to the variation in intermolecular interaction of the mesophase. The utility of the same complex is discussed. The phase width, thermal stability factor, tilt angle, phase transition temperature and its enthalpy values are reported.     

Synthesis of partially fluorinated poly(arylene ether sulfone) multiblock copolymers bearing perfluorosulfonic functions

Partially fluorinated poly(arylene ether sulfone) multiblock copolymers bearing perfluorosulfonic functions (ps‐PES‐FPES), with ionic exchange capacity (IEC) ranging between 0.9 and 1.5 meq H⁺/g, are synthesized by regioselective bromination of partially fluorinated poly(arylene ether sulfone) multiblock copolymers (PES‐FPES), followed by Ullman coupling reaction with lithium 1,1,2,2‐tetrafluoro‐2‐(1,1,2,2‐tetrafluoro‐2‐iodoethoxy)ethanesulfonate. The PES‐FPES are prepared by aromatic nucleophilic substitution reaction by an original approach, that is, “one pot two reactions synthesis.” The chemical structures of polymers are analyzed by ¹H and ¹⁹F NMR spectroscopy. The resulted ionomers present two distinct glass transitions and α relaxations revealing phase separation between the hydrophilic and the hydrophobic domains. The phase separation is observed at much lower block lengths of ps‐PES‐FPES as compared with the literature. AFM and SANS observations supported the phase separation, the hydrophilic domains are well dispersed but the connectivity to each other depends on the ps‐PES block lengths. The thermomechanical behavior, the water up‐take, and the conductivity of the ps‐PES‐FPES membranes are compared with those of Nafion 117^® and randomly functionalized polysulfone (ps‐PES). Conductivities close or higher to those of Nafion 117^® are obtained. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015 , 53, 1941–1956     

Optimized spacer layer thickness for plasmonic-induced enhancement of photocurrent in a-Si:H

Journal of Nanoparticle Research - Plasmonic interfaces consisting of silver nanoparticles of different sizes (50–100&;nbsp;nm) have been processed by the self-assembled dewetting...     

Formation and pharmacological activity of silicon—chitosan-containing glycerohydrogels obtained by biomimetic mineralization

The biomimetic sol—gel synthesis of silicon—chitosan-containing glycerohydrogels was carried out using silicon tetraglycerolate as a precursor. It was found that chitosan accelerates gel formation in weakly acidic media. In more acidic media, the kinetics of the process changes according to the curve with a maximum, which can be attributed to different mechanisms of silanol condensation before and after the isoelectric point. The investigated silicon—chitosan-containing glycerohydrogels exhibit antibacterial, anti-inflammatory, and wound healing activity. The synthesized hybrid glycerohydrogels are promising materials for biomedical applications.     

Near-Ultraviolet Circular Dichroism and Two-Dimensional Spectroscopy of Polypeptides

A fully quantitative theory of the relationship between protein conformation and optical spectroscopy would facilitate deeper insights into biophysical and simulation studies of protein dynamics and folding. In contrast to intense bands in the far-ultraviolet, near-UV bands are much weaker and have been challenging to compute theoretically. We report some advances in the accuracy of calculations in the near-UV, which were realised through the consideration of the vibrational structure of the electronic transitions of aromatic side chains.