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step decrease » sizes decrease (Expand Search), teer decrease (Expand Search), we decrease (Expand Search)
nn decrease » _ decrease (Expand Search), gy decreased (Expand Search), b1 decreased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
a step » _ step (Expand Search)
step decrease » sizes decrease (Expand Search), teer decrease (Expand Search), we decrease (Expand Search)
nn decrease » _ decrease (Expand Search), gy decreased (Expand Search), b1 decreased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
a step » _ step (Expand Search)
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1781
Mechanistic Investigation of the Hydrogenation of Ketones Catalyzed by a Ruthenium(II) Complex Featuring an N-Heterocyclic Carbene with a Tethered Primary Amine Donor: Evidence for...
Published 2011“…The complex [Ru(<i>p</i>-cymene)(<i>m</i>-CH<sub>2</sub>NH<sub>2</sub>)Cl]PF<sub>6</sub> (<b>1</b>) catalyzes the H<sub>2</sub>-hydrogenation of ketones in basic THF under 25 bar of H<sub>2</sub> at 50 °C with a turnover frequency (TOF) of up to 461 h<sup>−1</sup> and a maximum conversion of 99%. …”
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1782
Mechanistic Investigation of the Hydrogenation of Ketones Catalyzed by a Ruthenium(II) Complex Featuring an N-Heterocyclic Carbene with a Tethered Primary Amine Donor: Evidence for...
Published 2011“…The complex [Ru(<i>p</i>-cymene)(<i>m</i>-CH<sub>2</sub>NH<sub>2</sub>)Cl]PF<sub>6</sub> (<b>1</b>) catalyzes the H<sub>2</sub>-hydrogenation of ketones in basic THF under 25 bar of H<sub>2</sub> at 50 °C with a turnover frequency (TOF) of up to 461 h<sup>−1</sup> and a maximum conversion of 99%. …”
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1783
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1784
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1785
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1786
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1787
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1788
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1789
To be funny or not to be funny: Gender differences in student perceptions of instructor humor in college science courses
Published 2018“…<div><p>For over 50 years instructor humor has been recognized as a way to positively impact student cognitive and affective learning. …”
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1790
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1791
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1792
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1793
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1794
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1795
An Analysis of Porphyrin Molecular FlexibilityUse of Porphyrin Diacids
Published 1997“…Molecular mechanics calculations, using a modified version of MM2(87) and a newly developed force field for porphyrin diacids, correctly predict that the flexibility of <i>meso</i>-tetraaryl porphyrin diacids decreases as the steric bulk of the peripheral substituents increases: [H<sub>4</sub>TPyP]<sup>2+</sup> ≈ [H<sub>4</sub>TPP]<sup>2+</sup> > [H<sub>4</sub>T-2,6-(OH)<sub>2</sub> PP]<sup>2+</sup> ≈ [H<sub>4</sub>T-2,6-F<sub>2</sub> PP]<sup>2+</sup> > [H<sub>4</sub>T-2,6-Cl<sub>2</sub> PP]<sup>2+</sup> ≈ [H<sub>4</sub>TMP]<sup>2+</sup>. …”
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1796
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1797
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1798
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1799
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1800