185 research outputs found

    Replication Data for: Bird’s Decision to Shift the Direction of Migration Path Depends on the Position of Sun as well as Moon: A Directional Statistical Inference

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    Dataset for: Bird’s Decision to Shift the Direction of Migration Path Depends on the Position of the Sun as well as Moon: A Directional Statistical Inference (Author: Prithwish Ghosh, Debashis Chatterjee, Amlan Banerjee

    Mononuclear and dinuclear tetravalent zirconium compounds as catalysts for the synthesis of aliphatic polyesters and aliphatic polycarbonates

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    http://dx.doi.org/10.13039/501100001409 Department of Science and Technology, Ministry of Science and Technology, Indiahttp://dx.doi.org/10.13039/501100001843 Science and Engineering Research Boar

    Coordination induced fluorescence enhancement and construction of a Zn3 constellation through hydrolysis of ligand imine arms

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    The phenoxido and alkoxido bridged neutral Zn3 complex [Zn3(mu-H2bemp)2(m3-emp)2](1), with an angular Zn3(mu-OPh)2(mu-OEt)2 core and capping nitrogen donors, was synthesized via simultaneous chelation-cum-bridging of the parent and hydrolysed ligands. Zinc(II) coordination triggered the solution phase imine (C=N) bond hydrolysis of H3bemp (2,6-bis-[(2-hydroxyethylimino)methyl]-4-methylphenol) and yielded the unexpected angular trinuclear Zn(II) complex 1, having structural similarity with the Zn3 active site of P1 nuclease. H3bemp also displays a zinc(II) selective chelation-enhanced fluorescence response from strong metal ion coordination. Complexation of zinc(II) with H3bpmp (2,6-bis-[(3-hydroxypropylimino)methyl]-4-methylphenol), a close analogue of H3bemp,instead provides only mononuclear [Zn(H2bpmpHN)2](ClO4)2·2H2O(2·2H2O) (HN is the proton attached to an imine nitrogen atom) of two zwitterionic ligands, generated through a kind of coordination driven acid–base reaction, without showing any aggregation reaction. As the sole metal–organic precursor, both the complexes under pyrolytic conditions give ZnO nano structures of two morphologies

    Laboratory bioassay of insecticides mixtures (neonicotinoids and ketoenols) against Bemisia tabaci Asia I

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    Cotton leaves were dipped in serially diluted solutions of formulated insecticides for 10 s with slight agitation. The leaves with second instar nymphs that were dipped in double-distilled water containing 0.1 g L-1 Triton X-100 only, served as control. Each bioassay including control used 3-4 replicates at a minimum of eight different concentrations and were maintained at the controlled growth condition. All the insecticides concentrations were selected to give a range of 0-100% mortality of B. tabaci nymphs. Two weeks later final mortality was assessed when the last nymphal instar had been reached on control plants. It was computed by comparing the number of second instar nymphs present at the time of treatment with the number remaining dead or unhatched on the day of mortality assessment. For bioassays with synergists (PBO and DEF), the cotton leaves containing the second instar nymphs of B. tabaci were dipped into synergist solutions (100 mg L-1) for 10 s at least 2 h before the imposition of insecticide treatments. Other procedures were same to those with insecticides only

    Cluster

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    A mononuclear MnN4O2 complex with two zwitterionic li- gands and a centrosymmetric tetranuclear μ3-OH-bridged self-assembled Mn4 cluster were synthesized and charac- terized by using the [NO(H)N] ligand HOPhbip [2,6-bis(phen- ylmethyliminomethyl)-4-methylphenol]. The reaction in MeOH in the presence of NH4SCN and a lower stoichiometry of Mn(OAc)2·4H2O without any added base produces [MnII (HNbip)2(NCS)2]·CH3CN (1·CH3CN). In the presence of NaOH and NH4SCN in MeOH, the cluster [MnII 4(μ-bip)2(μ3-OH)2(NCS)4](2), featuring a stepped-cubane, was obtained through hydroxido-bridge-driven dimerization of two μ3-OH-bridged [Mn2] fragments derived from 1·CH3CN

    Eight deadly faux pas of continuous improvement

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