Infrared organic light emitting diodes using neodymium tris-(8-hydroxyquinoline) [PDF]
, 2000 Copyright 2000 American Institute of Physics. This article may be downloaded for personal use only. Any other use requires prior permission of the author and the American Institute of Physics.
Curry, RJ +3 more
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Acta Crystallographica Section E, 2011 In the reaction of 8-hydroxyquinoline, 2-methyl-8-hydroxyquinoline and stannic chloride, the 2-methyl-8-hydroxyquinoline is protonated, yielding the disolvated title salt, (C10H10NO)[SnCl4(C9H6NO)]·2CH3OH.
Ezzatollah Najafi +2 more
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Isolation and characterisation of 2-Tert-butyl-8-hydroxyquinoline as a crystalline solid and its blue fluorescent Li complex [PDF]
, 2014 Copyright © 2014 Poopathy Kathirgamanathan et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is ...
Blake, AJ +3 more
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The Crystal Structures of Metal 8-Hydroxyquinolinate. I. Copper 8-Hydroxyquinolinate [PDF]
Bulletin of the Chemical Society of Japan, 1963 Abstract The crystal structure of anhydrous copper 8-hydroxyquinolinate has been determined by the two-dimensional Fourier method. It is monoclinic and has been shown to belong to the B21/a space group, with eight molecules in a cell of the dimensions: a=23.66, b=8.72, c=15.30Å and β=117.5.
Fumikazu Kanamaru +2 more
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Elucidating the role of hyperfine interactions on organic magnetoresistance using deuterated aluminium tris(8-hydroxyquinoline) [PDF]
, 2009 Measurements of the effect of a magnetic field on the light output and current through an organic light emitting diode made with deuterated aluminium tris(8-hydroxyquinoline) have shown that hyperfine coupling with protons is not the cause of the ...
A. J. Drew +6 more
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Erbium (III) tris(8-hydroxyquinoline) (ErQ): A potential material for silicon compatible 1.5 mu m emitters [PDF]
, 1999 Copyright 1999 American Institute of Physics. This article may be downloaded for personal use only. Any other use requires prior permission of the author and the American Institute of Physics.
Curry, RJ, Gillin, WP
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1.54 mu m electroluminescence from erbium (III) tris(8-hydroxyquinoline) (ErQ)-based organic light-emitting diodes [PDF]
, 1999 Copyright 1999 American Institute of Physics. This article may be downloaded for personal use only. Any other use requires prior permission of the author and the American Institute of Physics.
Curry, RJ, Gillin, WP
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Bis{2-[1-(8-hydroxy-2-quinolylmethyl)-1H-benzimidazol-2-yl]quinolin-8-ol} toluene solvate
Acta Crystallographica Section E, 2010 Crystals of the title compound, 2C26H18N4O2·C7H8, were obtained from the reaction of 8-hydroxyquinoline with 1,2-phenylenediamine in methanol and recrystallized from toluene.
Qing-Ming Wang, Qi Ma, Hui-Li Chen
doaj +1 more source
Near-infrared photoluminescence of erbium tris(8-hydroxyquinoline) spin-coated thin films induced by low coherence light sources [PDF]
, 2007 Copyright 2007 AIP Publishing LLC. This article may be downloaded for personal use only. Any other use requires prior permission of the author and AIP Publishing. This article appeared in Applied Physics Letters [91, 021106 (2007)] and may be found at
Beleffi, GMT +5 more
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Restoration of susceptibility to amikacin by 8-hydroxyquinoline analogs complexed to zinc.
PLoS ONE, 2019 Gram-negative pathogens resistant to amikacin and other aminoglycosides of clinical relevance usually harbor the 6'-N-acetyltransferase type Ib [AAC(6')-Ib], an enzyme that catalyzes inactivation of the antibiotic by acetylation using acetyl-CoA as donor
Jesus Magallon +5 more
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