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31.
Abstract Acrylamide has been polymerized electrochemically in aqueous medium in the presence of tartaric acid, and the effects of such reaction variables as monomer concentration, electrolyte concentration, and current on the rates of polymerization have been studied. The mechanisms of initiation and termination have been discussed in the light of the observed kinetic data. Initiation is believed to occur through the generation of radical ions during electrolysis, and electrolytic termination is found to be negligible during the polymerization process. 相似文献
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Rajan Kumar Subir Kumar Ray Dr. Saikat Mukherjee Sudipta Saha Dr. Arijit Bag Prof. Dr. Pradip Kr. Ghorai Prof. Dr. Nirmalya Ghosh Prof. Dr. Raja Shunmugam 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(59):13514-13522
The development of organic photoluminescent materials, which show promising roles as catalysts, sensors, organic light-emitting diodes, logic gates, etc., is a major demand and challenge for the global scientific community. In this context, a photoclick polymerization method is adopted for the growth of a unique photoluminescent three-dimensional (3D) polymer film, E, as a model system that shows emission tunability over the range 350–650 nm against the excitation range 295–425 nm. The DFT analysis of energy calculations and π-stacking supports the spectroscopic observations for the material exhibiting a broad range of emission owing to newly formed chromophoric units within the film. Full polarization spectroscopic Mueller matrix studies were employed to extract and quantify the molecular orientational order of both the ground (excitation) and excited (emission) state anisotropies through a set of newly defined parameters, namely the fluorescence diattenuation and fluorescence polarizance. The information contained in the recorded fluorescence Mueller matrix of the organic polymer material provided a useful way to control the spectral intensity of emission by using pre- and post-selection of polarization states. The observation was based on the assumption that the longer lifetime of the excited dipolar orientation is attributed to the compactness of the film. 相似文献
34.
Jan-Christoph Eichler Robert A. Skutnik Anupam Sengupta Marco G. Mazza Martin Schoen 《Molecular physics》2019,117(23-24):3715-3733
Anisotropic fluids (e.g. liquid crystals) offer a remarkable promise as optofluidic materials owing to the directional, tunable, and coupled interactions between the material, flow, and the optical fields. Here we present a comprehensive in silico treatment of this anisotropic interaction by performing nonequilibrium molecular dynamics simulations. We quantify the response of a nematic liquid crystal (NLC) undergoing a Poiseuille flow in the Stokes regime, while being illuminated by a laser beam incident perpendicular to the flow direction. We adopt a minimalistic model to capture the interactions, accounting for two features: first, the laser heats up the NLC locally; and second, the laser polarises the NLC and exerts an optical torque that tends to reorient molecules of the nematic phase. Because of this reorientation the liquid crystal exhibits small regions of biaxiality, where the nematic director is one symmetry axis and the axis of rotation for the reorientation of the molecules is the other one. We find that the relative strength of the viscous and the optical torques mediates the flow-induced response of the biaxial regions, thereby tuning the emergence, shape and location of the regions of enhanced biaxiality. The mechanistic framework presented here promises experimentally tractable routes toward novel optofluidic applications based on material-flow-light interactions. 相似文献
35.
Qurratul Ain Sarvesh Kumar Pandey Om Prakash Pandey Soumitra Kumar Sengupta 《应用有机金属化学》2016,30(2):102-108
A series of neodymium(III) and samarium(III) complexes of type [Ln(L)Cl(H2O)3] have been synthesized with Schiff bases (LH2) derived from 3‐(phenyl/substituted phenyl)‐4‐amino‐5‐mercapto‐1,2,4‐triazoles and isatin. The structures of the complexes were established using elemental analysis, molar conductivities, magnetic moments, infrared, NMR (1H, 13C) and UV–visible spectra, X‐ray diffraction and mass spectrometry. The thermal behaviour of these compounds under non‐isothermal conditions was investigated using thermogravimetry and differential thermogravimetry. The intermediates obtained at the end of various thermal decomposition steps were identified from elemental analysis and infrared spectral studies. All the ligands and their complexes were also screened for their antibacterial activity against Staphylococcus aureus and Bacillus subtilis and antifungal activity against Aspergillus niger, Aspergillus flavus and Colletotrichum capsici. The screening results were correlated with the structural features of the compounds. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
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37.
Ester Abtew Abraham J. Domb Arijit Basu 《Journal of polymer science. Part A, Polymer chemistry》2017,55(16):2657-2662
We report on the synthesis of polypeptides with saccharide side chains starting from d ‐glucosaminic acid. The hydroxyl groups were first protected by benzylation, followed by N‐carboxyanhydride formation, which was polymerized by ring opening to form a high molecular weight polyamide. De‐protection of the benzyl groups yields a polypeptide with fully de‐protected saccharide side chains. The resulting new non‐ionic, water soluble, and optically active polymers possessing the properties of both peptides and saccharides have potential use as scaffolds for tissue engineering and drug carriers. The method described here may be extended to any saccharide α‐amino acid. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55, 2657–2662 相似文献
38.
Rh-Catalyzed intramolecular C-H insertion reaction of L-leucine derived α-diazoketone is described. 相似文献
39.
An equivalent circuit model of uni-traveling carrier photodiode (UTC-PD) is developed from integral carrier density rate equation and few important properties of the device such as the electrical and optical characteristics are evaluated by employing advanced device physics. Circuit model incorporates chip and package parasitic of the device quite simply to provide practical behaviour of UTC-PD. We have developed small signal ac circuit model which is useful for the analysis of low power modulation characteristics of the device and dc circuit model which is advantageous to find wavelength dependent responsivity fairly accurately. At high optical input power the device bandwidth is found to be increased through enhancement of self-induced field in the absorption region and high output power can be derived from the device when absorption width is large. Such condition calls for large signal analysis. We have developed large signal circuit model by combining few mathematical transformations with small signal circuit model with different circuit element values. Our large signal model is unique that the same circuit can be used for both small and large signal analysis. With large signal model the optical power induced bandwidth improvement and output photocurrent saturation are explained. Large signal model is validated through linearity and IP3 analysis which found close agreement with the measured results. 相似文献
40.
A. Sengupta B. Rajeswari R. M. Kadam R. J. Kshirsagar 《Journal of Radioanalytical and Nuclear Chemistry》2012,292(2):903-908
The use of serpentine as a potential nuclear shielding material necessitates a chemical quality control of the samples before
its use in reactors. With this in view, characterization of these mineral samples was carried out using inductively coupled
plasma atomic emission spectrometry (ICP-AES) and Instrumental neutron activation analysis (INAA) methods. The analytical
results obtained by both ICP-AES and NAA techniques were found to be comparable. Na, Cr, Co, Zn, and Cu were found to be present
in all samples of Indian origin while Ga, Ag, Ni, and Cd were found to below the limits of detection. A comparison on the
detection limits of elements of interest was also carried out by both the analytical techniques and found to be in good agreement.
An infrared spectroscopic investigation was also carried out on all the mineral samples. Bands at 3,689 and 3,648 cm−1 were attributed to inner and outer hydroxyl stretching of Mg–OH, respectively. The weak and broad band centered around 3,416 cm−1 was assigned due to the stretching vibrations of the adsorbed water molecules while three bands at 1076, 1022 and 968 cm−1 were prescribed to the vibrations of the SiO4 tetrahedra. 相似文献