Showing 109,521 - 109,527 results of 109,527 for search '(( 10 ((we decrease) OR (teer decrease)) ) OR ( 50 ((mean decrease) OR (a decrease)) ))', query time: 1.03s Refine Results
  1. 109521
  2. 109522

    Reductive Cleavage of Acyl Halides to Carboxylato Alkylidyne Complexes from Their Reactions with the Quintuply Bonded Dimolybdenum Amidinate by N. V. Satyachand Harisomayajula (2611348)

    Published 2016
    “…Complexes <b>3</b>–<b>7</b> were subsequently treated with acyl halides RC­(O)­X to undergo haloacylation and yield carbyne-bridged dimolybdenum species [Mo<sub>2</sub>(X)­(μ-X)­(μ-CR)­(κ<sup>2</sup>-O<sub>2</sub>CR)­(μ-κ<sup>2</sup>-HC­(N-2,6-<sup><i>i</i></sup>Pr<sub>2</sub>C<sub>6</sub>H<sub>3</sub>)<sub>2</sub>)<sub>2</sub>] (R = Me, X = Cl (<b>10</b>); R = C<sub>6</sub>H<sub>5</sub>, X = Cl (<b>11</b>), Br (<b>12</b>); R = 4-FC<sub>6</sub>H<sub>4</sub>, X = Cl (<b>13</b>); R = 2-MeC<sub>6</sub>H<sub>4</sub>, X = Cl (<b>14</b>)). …”
  3. 109523

    Reductive Cleavage of Acyl Halides to Carboxylato Alkylidyne Complexes from Their Reactions with the Quintuply Bonded Dimolybdenum Amidinate by N. V. Satyachand Harisomayajula (2611348)

    Published 2016
    “…Complexes <b>3</b>–<b>7</b> were subsequently treated with acyl halides RC­(O)­X to undergo haloacylation and yield carbyne-bridged dimolybdenum species [Mo<sub>2</sub>(X)­(μ-X)­(μ-CR)­(κ<sup>2</sup>-O<sub>2</sub>CR)­(μ-κ<sup>2</sup>-HC­(N-2,6-<sup><i>i</i></sup>Pr<sub>2</sub>C<sub>6</sub>H<sub>3</sub>)<sub>2</sub>)<sub>2</sub>] (R = Me, X = Cl (<b>10</b>); R = C<sub>6</sub>H<sub>5</sub>, X = Cl (<b>11</b>), Br (<b>12</b>); R = 4-FC<sub>6</sub>H<sub>4</sub>, X = Cl (<b>13</b>); R = 2-MeC<sub>6</sub>H<sub>4</sub>, X = Cl (<b>14</b>)). …”
  4. 109524

    LRIG1 and CDK6 expression in the lateral ventricular wall cells by Hyung-song Nam (8914220)

    Published 2025
    “…The adherent culture technique is from <a href="https://doi.org/10.1093/cercor/bhj167" rel="noreferrer" target="_blank">Pollard et al., 2006</a>. …”
  5. 109525

    Fluorescent Molecular Rotors of Organoboron Compounds from Schiff Bases: Synthesis, Viscosity, Reversible Thermochromism, Cytotoxicity, and Bioimaging Cells by Marisol Ibarra-Rodrı́guez (3750316)

    Published 2017
    “…We report the design, synthesis, and characterization of two new fluorescent molecular rotors of boron derived from Schiff bases: (2,4,8,10-tetra-<i>tert</i>-butyl-6-phenyldibenzo­[<i>d,h</i>]­[1,3,6,2]­dioxazaboronine (<b>3</b>) and 1,4-bis­(2,4,8,10-tetra-<i>tert</i>-butyldibenzo­[<i>d,h</i>]­[1,3,6,2]­dioxazaboronin-6-yl)­benzene (<b>4</b>), as well as the free ligand 2-[[(3,5-di-<i>tert</i>-butyl-2-hydroxyphenyl)­imino]­methyl]-4,6-di-<i>tert</i>-butylphenol <b>1</b>. …”
  6. 109526
  7. 109527