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

    Chelate and trans effect of P,O donor phosphine ligands on rhodium catalyzed carbonylation of methanol

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    Four complexes of the type [Rh(CO)Cl(�2-P,O-L)](1a,1b) and [Rh(CO)Cl(�1-P-L)2](2a,2b), where L = Ph2PC6H4-2-OCH3(a) and Ph2PC6H4-2-CH2OCH3(b), have been synthesized by the reaction of [Rh(CO)2Cl]2 with appropriate mol equivalents of the ligands in CH2Cl2. The complexes show single intense �(CO) bands in the range 1965–1989 cm−1 indicating the presence of terminal carbonyl groups. All the complexes have been characterized by elemental analyses, mass spectrometry, IR and multinuclear NMR (1H, 31P and 13C) spectroscopy, and the molecular structure of the ligand b is determined by single crystal X-ray diffraction. The complexes undergo oxidative addition (OA) with excess CH3I to afford Rh(III)-acyl complexes of the type [RhCl(COCH3)I(L)](3a,3b) and [RhCl(COCH3)I(L)2](4a,4b). The kinetic data for the OA reactions with CH3I indicate a first order reaction and also exhibit that the rate of OA for the chelate complexes (1a and 1b) is higher than those of trans-complexes (2a and 2b). The catalytic efficiencies of 1a, 1b, 2a and 2b in carbonylation of methanol exhibit higher Turn Over Frequency (TOF) 689–1808 h−1 than the well-known Monsanto’s species [Rh(CO)2I2]− (TOF = 464–1000 h−1) under similar experimental conditions. The catalytic activities vary in the order as 1a > 1b > 2a > 2

    Efficient clay supported Ni0 nanoparticles as heterogeneous catalyst for solvent-free synthesis of Hantzsch polyhydroquinoline

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    A green and efficient multicomponent one-pot synthesis of Hantzsch polyhydroquinoline was achieved by the condensation of aldehydes, dimedone, ethylacetoacetate and ammonium acetate at room temperature using environmentally benign modified Montmorillonite supported Ni0-nanoparticles as catalyst. The well dispersed Ni0-nanoparticles having a high surface to volume ratio have promising features for the reaction such as easy removal of the catalyst, solvent-free, shorter reaction time, high product yields (about 95%) and easy work up procedure. There is no significant effect of electron withdrawing or donating nature of substituent on aldehydes in the formation of polyhydroquinoline derivatives

    Alpha 1 antitrypsin gene: A case-control study in chronic obstructive pulmonary disease

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    Alpha-1 antitrypsin (AAT) deficiency is an inherited disorder that causes low levels of, or no AAT in the blood. The most common illness in adults with AAT deficiency is lung disease during the third and fourth decades of life. Most commonly, it is associated with chronic obstructive pulmonary disease (COPD). Mutations in the protease inhibitor (PI) gene, located on chromosome 14, are associated with this genetic disorder. The Z protein is due to a single amino acid substitution of 342 glutamine lysine. Although cigarette smoking is the main environmental risk factor, only about 15% of smokers develop clinically significant disease suggesting other influences on disease expression. The study included hospital based age and sex matched 100 cases of COPD and 100 controls without COPD recruited from Christian Medical Centre, Jorhat, Assam. These cases were recruited from February 2009 to December 2009. Subjects were included in the COPD group on the basis of lung function test. DNA extraction was done by DNA extraction kit and amplification for AAT gene was done by site directed mutagenesis polymerase chain reaction (PCR) method as described by Tazellar et al. (1992). We found that smoking was the prior cause of COPD. A1AT deficiency is not prevalent in our population subset but certain other genes could be the attributable factor for COPD

    Studies on the influence of host plants and effect of chemical stimulants on the feeding behavior in the muga silkworm, Antheraea assamensis

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    The feeding habits of Antheraea assamensis, Helfer (Lepidoptera: Saturniidae) larvae towards the leaves of its four different host plants, Persea bombycina King ex. Hook (Laurales: Lauraceae), Litsea polhantha Jussieu, L. salicifolia Roxburgh ex. Nees and L. citrata Blume, and the chemical basis of feeding preference were investigated. Nutritional superiority of young and medium leaves with respect to soluble protein, total phenol and phenylalanine ammonia lyase activity was observed in the leaves of P. bombycina compared to other host plants. Attraction and feeding tests with detached leaves and artificial diet with different chemical stimulants revealed that a mixture of the flavonoids, myrcetin, and 7, 2’, 4’ trimethoxy dihydroxy flavone with sterol compound β-sitosterol elicited the most biting behavior by A. assamensis larvae. While linalyl acetate alone attracted larvae towards the leaves of the host plants, a mixture of caryophyllene, decyl aldehyde and dodecyl aldehyde was found to both attract them to the host leaves and cause biting behavior. Azaindole was found to deter them from the host plants

    Microwave assisted solvent free synthesis of 1,3-diphenylpropenones

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    In-vitro antioxident and free radical scavenging activity of Alternanthera sessilis

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    The present study was aimed to evaluate the antioxidant activity of A.sessilis plant extracts in different solvents. The antioxidant activity was studied by phosphomolybdate method and DPPH method. In phosphomolybdate method the highest activity was shown by methanolic extract (12.044 mM of ascorbic acid eqvt/gm of sample). The highest radical scavenging activity by DPPH method was found in methanol extracts (IC 50 587.093µg/ml). Ferrous chelating activity, superoxide radical scavenging activity, nitric oxide radical scavenging activity was found high in acetone, acetone and methanol extracts respectively. Total Flavonoids and crude phenolics were found to be 0.370 mg/gm dry wt. and 1.529 mg/gm dry wt. respectively. The antioxidant activity increases with increase in the concentration. This study indicates that A.sessilis is a potential source of natural antioxidant

    Rhodium(I) carbonyl complexes of tetradentate chalcogen functionalized phosphines, [P/(X)(CH2CH2P(X)Ph2)3] {X = O, S, Se}: Synthesis, reactivity and catalytic carbonylation reaction

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    The reaction of [Rh(CO)2Cl] 2 with 0.5 mol equivalent of the ligands [P0(X)(CH 2eCH 2P(X)Ph 2) 3](P0P 3X 4) {where X � O(a), S(b) and Se(c)} affords tetranuclear complexes of the type [Rh 4(CO) 8Cl 4(P0P 3X 4)] (1ae1c). The complexes 1ae1c have been characterized by elemental analyses, mass spectrometry, IR and multinuclear NMR spectroscopy, and the ligandsb andc are structurally determined bysingle crystal X-ray diffraction.1ae1c undergo oxidative addition (OA) reactions with CH3I to generate Rh(III) oxidised products. Kinetic data for the reaction of 1a and 1b with excess CH 3I indicate a pseudo�01rst order reaction. The catalytic activity of 1ae1c for the carbonylation of methanol to acetic acid and its ester show a higher Turn Over Frequency (TOF � 1349e1748 h �021) compared to the well-known species [Rh(CO)2I2] �02 (TOF � 1000 h�021) under the similar experimental conditions. However, 1b and 1c exhibit lower TOF than 1a, which may be due to the desulfurization and deselinization of the ligands in the respective complexes under the reaction conditions

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