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1.
Parthiban A. Lingam K. Arun Prasath Mangalaraj S. Muthukrishnan P. Surendiran M. 《Journal of Cluster Science》2021,32(5):1401-1409
Journal of Cluster Science - Single crystal electron paramagnetic resonance (EPR), powder X-ray diffraction (XRD), Fourier transform-infrared (FT-IR) and UV–Visible (UV–Vis)... 相似文献
2.
Bayrakdar Alpaslan Mert Samet Kasımoğulları Rahmi Bangaru Sathya Manivannan Prasath 《Research on Chemical Intermediates》2022,48(5):2087-2109
Research on Chemical Intermediates - Trifluoromethyl group containing pyrazole-3-carboxamide derivative is synthesized and the structure of the molecule (E3N5PC) has been verified by using FT-IR,... 相似文献
3.
Siti Aini Binti Nordin Mohan Prasath Mani Ahmad Zahran Md Khudzari Ahmad Fauzi Ismail 《International Journal of Polymer Analysis and Characterization》2020,25(3):126-133
AbstractWound healing is a complex process and it involves restoration of damaged skin tissues. Several wound dressings comprising naturally made substances are constantly investigated to assist wound healing. In this research, a new wound dressing based on polyurethane (PU) supplemented with essence of Channa striatus (CS) fish oil was made by electrospinning. Morphological study depicted the reduction in fiber diameter than PU with the addition of fish oil (0.552?±?0.109?μm for 8:1 v/v% and 0.519?±?0.196?μm 7:2 v/v%) than the pristine PU (0.971?±?0.205?µm). Fourier transform infrared spectroscopy (FTIR) analysis revealed the presence of fish oil in the composite as identified through increasing peak intensity. Fish oil resulted in the hydrophilic behavior (88?±?3 (8:1 v/v) and 70?±?6 (7:2 v/v)) as revealed in the contact angle analysis. Thermal gravimetric analysis (TGA) showed the superior thermal behavior of the wound dressing patch compared to the PU. Atomic force microscopy (AFM) analysis insinuated a decrease in the surface roughness of the pristine polyurethane with the added fish oil. Coagulation assays signified the delay in the blood clotting time portraying its anti-thrombogenic behavior. Hemolytic assay revealed the less toxic nature of the developed nanocomposites with the red blood cells (RBC’s) depicting its safety with blood. Hence, polyurethane nanofibers supplemented with fish oil made them as deserving candidates for wound dressing application. 相似文献
4.
Two types of β‐ functionalized (mono nitrated and perbrominated) meso tetrakis(5‐halothien‐;2‐yl)porphyrins, which can be used as precursors for the synthesis of other asymmetric and highly substituted porphyrins, have been synthesised and characterized. Introduction of a nitro group at the β‐ position shifted soret band 11–16 nm to the red region and redox potentials to > 170 mV for oxidation and > 250 mV for reduction anodically. Perbromination of halothienylporphyrins lead to enhanced bathochromically shifted uv‐visible spectral bands, but had only marginal influence on oxidation potentials. Effect of mono nitro group and eight bromo groups on the electronic properties of the porphyrins is attributed, respectively to, the electron deficiency created in the porphyrin π‐ system and the nonplanar conformation induced by the bulky bromo groups. 相似文献
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A method to prepare 1H-indole-2-carbaldehydes and (E)-2-(iodomethylene)indolin-3-ols by gold(I)-catalyzed cycloisomerization of 1-(2-(tosylamino)phenyl)prop-2-yn-1-ols with N-iodosuccinimide (NIS) is reported. The reactions were shown to be operationally simplistic and proceed efficiently for a wide variety of substrates, affording the corresponding products in good to excellent yields (70-99%). The mechanism is suggested to involve activation of the alkyne moiety of the substrate by the gold(I) catalyst. This triggers intramolecular addition of the tethered aniline moiety to give a vinyl gold intermediate, which undergoes iododeauration with NIS to give the (E)-2-(iodomethylene)indolin-3-ol adduct. Subsequent 1,3-allylic alcohol isomerization (1,3-AAI) followed by formylation of this vinyl iodide intermediate then gives the 1H-indole-2-carbaldehyde. 相似文献
7.
N. Kalaiselvi M. Ashok Kumar M. S. Prasath N. G. Renganathan M. Raghavan N. Muniyandi 《Ionics》2002,8(5-6):447-452
Li2CoMn3O8, a 5 V cathode material used in rechargeable lithium batteries, has been synthesized by adopting a novel technique of using
fuels along with the nitrate reactants. The effect of the fuel on the synthesis of Li2CoMn3O8 has been analyzed in terms of the physical and electrochemical properties of the final product formed by various methods
such as solid-state carbonate fusion and the solution route using acetate and nitrate precursors. Powder X-ray diffraction
FT IR spectrum, particle size, surface area and SEM analysis were carried out. The combustion method, also known as selfpropagating
high temperature (SPHT) method, has been employed in the present study by using nitrate mixtures of the respective salts and
a nitrogeneous fuel (urea or glycine) at a temperature of 300 °C for 3 hrs. The nitrate reactants without the addition of
fuel gave only a deliquescent product even at elevated temperature (600 °C) thus indicating the necessity of fuels. Similar
attempts using acetate reactants with and without the addition of nitrogeneous fuels were made separately in order to find
out the necessity of fuel also in this case. The characterization of the product in terms of purity, single-phase formation
and surface morphology suggested that the fuel played no role in the case of the acetate precursors. A comparative study was
made on the products obtained by the acetate precursor, combustion method and the conventional carbonate method. Among the
three methods, the combustion method with glycine as fuel yielded the spinel phase with high purity Li2CoMn3O8 with superior electrochemical behavior both in terms of high cell voltage and good cycle life behavior. 相似文献
8.
Prasath Kothandaraman 《Tetrahedron》2009,65(9):1833-454
A highly efficient gold- and silver-catalyzed allylic alkylation of 1,3-dicarbonyl compounds with allylic alcohols has been developed. The reaction was shown to proceed expediently for a wide variety of 1,3-dicarbonyl compounds and allylic alcohols, including 1° and terminal ones, under very mild conditions at room temperature in good to excellent yields (55-96%). 相似文献
9.
The synthesis, characterization, and redox and spectral properties of the meso‐5,10,15,20‐tetrakis(2′‐chlorobenzoquinolin‐3′‐yl)porphyrin are reported. The synthesis of the porphyrin was performed by following the modified Lindsey procedure, and its zinc(II) derivative was prepared by using the conventional method. The electronic properties of the compound were investigated by cyclic voltammetry and spectroscopy. This compound shows unusual redox behavior with difficulty in oxidation and ease of reduction compared to tetraphenylporphyrin. 相似文献
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