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PVD preparation and spectral study of organic electroluminescent material 8-hydroxyquinoline lithium
Juncong He +6 more
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Antimony 8-hydroxyquinolinates
Australian Journal of Chemistry, 1968Precipitation from homogeneous solution or by conventional means with 8-hydroxyquinoline in the presence of tartaric acid has been successfully employed for the determination of antimony. The complex produced corresponds to the formula SbOQ,2HQ.
TJ Cardwell +3 more
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Analytica Chimica Acta, 1968
Abstract The preparation of two yttrium 8-hydroxyquinolinates, one by conventional means and the other by precipitation from homogeneous solution, was investigated. Analytical data indicated that the complex prepared conventionally corresponds to Y(C9H6NO)3, and the complex prepared by precipitation from homogeneous solution corresponds to Y(C9H6NO)3·
Terence J. Cardwell, Robert J. Magee
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Abstract The preparation of two yttrium 8-hydroxyquinolinates, one by conventional means and the other by precipitation from homogeneous solution, was investigated. Analytical data indicated that the complex prepared conventionally corresponds to Y(C9H6NO)3, and the complex prepared by precipitation from homogeneous solution corresponds to Y(C9H6NO)3·
Terence J. Cardwell, Robert J. Magee
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Spectrochimica Acta Part A: Molecular Spectroscopy, 1984
Abstract This paper reports the electronic absorption spectrum of 8-hydroxyquinoline in the liquid and vapour states in the region 50 000-28 000 cm −1 and the i.r. absorption spectrum in the region 400–4000 cm −1 in KBr and in the neat liquid.
S.L. Srivastava +2 more
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Abstract This paper reports the electronic absorption spectrum of 8-hydroxyquinoline in the liquid and vapour states in the region 50 000-28 000 cm −1 and the i.r. absorption spectrum in the region 400–4000 cm −1 in KBr and in the neat liquid.
S.L. Srivastava +2 more
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Tumor-targeted delivery of 8-hydroxyquinoline
International Journal of Radiation Oncology*Biology*Physics, 1991RIF-1 mouse tumors express high levels of beta-glucuronidase activity relative to most normal tissues. The high activity can be exploited for targeting specific drugs preferentially to tumor tissues. In this study we examined the kinetics of 8-hydroxyquinoline (8-OHQ) accumulation in tumor and in several normal tissues resulting from the in vivo ...
T P, Monson +3 more
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Chloromethylation of 8-hydroxyquinoline
Analytica Chimica Acta, 1956Abstract The reaction of formaldehyde on a hydrochloric acid solution of 8-hydroxyquinoline, in the presence of hydrochloric acid gas, gave a chloromethyl derivative which is probably 7-chloromethyl-8-hydroxyquinoline hydrochloride. This compound is readily converted into the 7-hydroxymethyl derivative in alkaline solution.
Quintus Fernando +2 more
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ChemInform Abstract: Carboxylation of 8‐Hydroxyquinoline to 8‐Hydroxyquinoline‐7‐carboxylic Acid.
ChemInform, 1995AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
V. V. RAGULIN +2 more
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Dalton Transactions, 2006
The spectroscopy, electrochemistry, and electrogenerated chemiluminescence (ECL) of [(q)(qH)Li]x (qH=8-hydroxyquinolinato) and [(Meq)(MeqH)Li]x (MeQH=2-methyl-8-hydroxyquinolinato) have been investigated. In both acetonitrile and aqueous solutions, [(q)(qH)Li]x and [(Meq)(MeqH)Li]x have absorption maxima at 320 and 309 nm, respectively. When excited at
David J, Vinyard, Mark M, Richter
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The spectroscopy, electrochemistry, and electrogenerated chemiluminescence (ECL) of [(q)(qH)Li]x (qH=8-hydroxyquinolinato) and [(Meq)(MeqH)Li]x (MeQH=2-methyl-8-hydroxyquinolinato) have been investigated. In both acetonitrile and aqueous solutions, [(q)(qH)Li]x and [(Meq)(MeqH)Li]x have absorption maxima at 320 and 309 nm, respectively. When excited at
David J, Vinyard, Mark M, Richter
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The Journal of Chemical Thermodynamics, 1989
Abstract The standard (po = 0.1 MPa) molar enthalpies of combustion, in oxygen, at 298.15 K, were measured by static bomb calorimetry for three 8-hydroxyquinolines; the vapour pressures of the crystals were measured as functions of temperature by the Knudsen-effusion technique, and the standard molar enthalpies of sublimation, at 298.15 K, were ...
Manuel A.V. Ribeiro da Silva +2 more
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Abstract The standard (po = 0.1 MPa) molar enthalpies of combustion, in oxygen, at 298.15 K, were measured by static bomb calorimetry for three 8-hydroxyquinolines; the vapour pressures of the crystals were measured as functions of temperature by the Knudsen-effusion technique, and the standard molar enthalpies of sublimation, at 298.15 K, were ...
Manuel A.V. Ribeiro da Silva +2 more
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Spectrochimica Acta, 1956
Abstract The infra-red absorption spectra of solid 8-hydroxyquinoline, 2-methyl-8-hydroxyquinoline, 4-methyl-8-hydroxyquinoline, and of a number of metal chelates derived from these reagents, have been studied. In general, the spectra of the metal chelates derived from a given reagent were found to be quite similar.
Robert G. Charles +4 more
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Abstract The infra-red absorption spectra of solid 8-hydroxyquinoline, 2-methyl-8-hydroxyquinoline, 4-methyl-8-hydroxyquinoline, and of a number of metal chelates derived from these reagents, have been studied. In general, the spectra of the metal chelates derived from a given reagent were found to be quite similar.
Robert G. Charles +4 more
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