Results 151 to 160 of about 2,136,561 (347)
Generalized de Moivre's theorem, quaternions, and Lorentz transformations on a Minkowski space
I.S. Reed
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Herein, electrocatalytic activity enhancement is reported of NiCoP nanorods by applying an external magnetic field. The NiCoP nanorods exhibit an overpotential of 100 mV at 10 mA cm−2 without magnetic field. However, under low magnetic field of 2000 G, the overpotential reduces to 62 mV at 10 mA cm−2 in 0.5 M H2SO4, demonstrating that external magnetic
Vishwanath Ankalgi+7 more
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Electroweak Interaction Model with an Undegenerate Double Symmetry
The initial P-invariance of the electroweak interaction Lagrangian together with the low-energy results of the Weinberg-Salam model is provided by a local secondary symmetry.
Leonid M. Slad
doaj
Bi/BiOBr/P25 TiO2 composites are synthesized via a solvothermal method incorporating 1 wt% of a carbon‐based material (graphene oxide [GO], graphene, carbon nanotubes, or buckminsterfullerene). The GO–based composite exhibits the highest photocatalytic NOx removal efficiency (≈22% NO and ≈15% NO2) with these synergetic improvements attributed to ...
Paransa Alimard+7 more
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Phosphine‐Ligated Cobalt(II) Acetylacetonate Complexes
Phosphines can react with cobalt acetylacetonate or Co(acac)2 to give products with drastically different structures. Depending on the ligand properties, phosphine‐ligated cobalt(II) acetylacetonate complexes can be mononuclear, dinuclear, or polymeric, 5‐coordinate or 6‐coordinate, and with or without hydrogen–bonding interactions. Monophosphines bind
J. P. I. Dulmini Jayawardhena+2 more
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On the question of temperature transformations under Lorentz and Galilei boosts [PDF]
Geoffrey L. Sewell
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Iron complexes bearing cyclopentadienone/hydroxycyclopentadienyl and NHC ligands in combination with carbonyls are active in ammonia–borane dehydrogenation. In situ IR and scale up experiments give insight in the catalytic mechanism. Carbonyl iron complexes, bearing cyclopentadienone/hydroxycyclopentadienyl ligands and N‐heterocyclic carbene as ...
Andrea Cingolani+10 more
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The planar‐chiral stannylated diaminoferrocene [Fe{η5‐C5H3‐1‐(SnnBu3)‐2‐(NH2)}{η5‐C5H4(NH2)}] (A) and its diimine derivative [Fe{η5‐C5H3‐1‐(SnnBu3)‐2‐(N=CHPh)}{η5‐C5H4(N=CHPh)}] (B) gave unsatisfactory results in attempts to achieve Stille cross‐coupling reactions with PhBr in the presence of [PdCl2(PPh3)2] or [Pd(PPh3)4]/CuO as catalysts.
Johannes Blanckenberg+2 more
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