IR@NEIST - North East Institute of Science and Technology (CSIR)
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    339 research outputs found

    Dicarbonylrhodium(I) complexes of pyridine alcohol ligands and their catalytic carbonylation reaction

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    Reaction of dimeric complex [Rh(CO)2Cl]2 with two molar equivalent of pyridine alcohol ligands (L) like 2-hydroxymethylpyridine (a), 3-hydroxymethylpyridine (b) and 4-hydroxymethylpyridine (c) afford the rhodium(I) dicarbonyl complexes [Rh(CO)2ClL](1a–c). The ligands are coordinated to the metal center through N-donor site. The complexes 1 undergo oxidative addition (OA) reactions with various alkyl halides (RI) like CH3I, C2H5I to produce Rh(III)complexes of the type [Rh(CO)(COR)IClL], where R = –CH3(2), –C2H5(3). Kinetic data for the reaction of 1 with CH3I indicate a first order reaction. The catalytic activity of the complexes 1 in the carbonylation of methanol was higher than that of the well known species [Rh(CO)2I2]−

    Meeting report - Sericulture and viable technologies for better silk production

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    RDF (X-ray) Analysis of Tirap Coal

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    Study on the reactive extraction and stripping kinetics of certain �-lactam antibiotics

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    The extraction equilibrium and stripping of certain �-lactam antibiotics such as 7-aminocephalosporanic acid (7-ACA), 7-aminodeacetoxy cephalosporanic acid (7-ADCA), 6-aminopenicillanic acid (6-APA), cephalosporin-C (CPC) and cephalexin from aqueous solution of phosphate and carbonate buffers were studied with Aliquat-336 (tricaprylylmethylammonium chloride) dissolved in n-butylacetate as the solvent over an aqueous phase pH range of 5–10. The extraction equilibrium constant Kp was found to increase with aqueous phase pH, which is attributed to the increase in ionisation of the �-lactam. A systematic study on kinetic of stripping or re-extraction of 7-ADCA and cephalexin from the extracted phase was carried out using an aqueous solution of citrate buffer at different pH values and was found to be pH dependent which is also attributable to ionisation behaviour of the �-lactams. Such observation is considered important, as re-extraction at an appropriate pH value is possible. The rate of stripping was found to be weakly dependent on Cl− concentration of the aqueous phase and the same was analysed with a simple mass transfer model based on film theory

    Indium(III) trifluoromethanesulfonate: An efficient reusable catalyst for the alkynylation-cyclization of 2-aminoaryl ketones and synthesis of 2,4-disubstituted quinolines

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    An environmentally friendly and highly efficient procedure for the preparation of 2,4-disubstituted quinoline derivatives has been developed by a simple alkynylation 13cyclization reaction of 2-aminoaryl ketones with phenylacetylenes in the presence of indium( III) trifluoromethanesulfonate In(OTf)3 under microwave irradiation and solvent-free conditions. This catalyst can be recovered after the reaction and reused efficiently in subsequent runs

    Propensity of citric, maleic, oxalic and succnic acids for the acquous solution- vapour interface : Surface tension measurment and molecular dynamics simulations

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    Behaviour of oxalic, citric, succinic, and maleic acids at the air/water interface is characterized and quantified by surface tension measurements in a broad concentration range and molecular dynamics simulations in slab geometry employing a polarizable force field. The relative order of surface propensities of these atmospherically relevant acids is established in this study with results being also in a very good agreement with previous measurements

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    IR@NEIST - North East Institute of Science and Technology (CSIR)
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