Results 161 to 170 of about 6,419,791 (211)
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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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8‐Hydroxyquinoline Fluorophore for Sensing of Metal Ions and Anions
The chemical record, 2020Among various known hydroxyquinolines, 8‐hydroxyquinoline (8‐HQ) is the most prevalent moiety due to excellent property for the formation of the complex with different metal ions and anions, and utilized in a wide variety of applications in ...
Rohini, Kamaldeep Paul, Vijay Luxami
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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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Chemical Communications, 2020
The N and O atoms in the bidentate ligand 8-hydroxyquinoline (8-HQ) can simultaneously coordinate with Sn2+, which greatly inhibits the oxidation of Sn2+.
Zhuojia Lin +6 more
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The N and O atoms in the bidentate ligand 8-hydroxyquinoline (8-HQ) can simultaneously coordinate with Sn2+, which greatly inhibits the oxidation of Sn2+.
Zhuojia Lin +6 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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Spectrochimica Acta Part A: Molecular Spectroscopy, 1975
Abstract The thermodynamic dissociation constants for the deprotonation and dissociation steps of 8-hydroxyquinoline, 5-chloro-8-hydroxyquinoline and 5-nitro-8-hydroxyquinoline in the temperature range 20–60°C have been determined by the spectrophotometric method.
C. Klofutar, Š. Paljk, F. Krašovec
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Abstract The thermodynamic dissociation constants for the deprotonation and dissociation steps of 8-hydroxyquinoline, 5-chloro-8-hydroxyquinoline and 5-nitro-8-hydroxyquinoline in the temperature range 20–60°C have been determined by the spectrophotometric method.
C. Klofutar, Š. Paljk, F. Krašovec
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, 2020
Two newly substituted methylquinolin-8-ol derivatives, namely 5-((aminooxy) methyl) quinolin-8-ol (AMQN) and 5-(hydrazinylmethyl) quinolin-8-ol (HMQN) was synthesized and characterized by ‘IR’ and NMR spectroscopy.
Z. Rouifi +8 more
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Two newly substituted methylquinolin-8-ol derivatives, namely 5-((aminooxy) methyl) quinolin-8-ol (AMQN) and 5-(hydrazinylmethyl) quinolin-8-ol (HMQN) was synthesized and characterized by ‘IR’ and NMR spectroscopy.
Z. Rouifi +8 more
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Journal of Molecular Liquids, 2019
Two new organic compounds based on 8-hydroxyquinoline have been successfully synthesized, and characterized by FT-IR, 1H, 13C NMR and Elemental analysis.
M. Faydy +6 more
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Two new organic compounds based on 8-hydroxyquinoline have been successfully synthesized, and characterized by FT-IR, 1H, 13C NMR and Elemental analysis.
M. Faydy +6 more
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, 2019
Two new 8-hydroxyquinoline derivatives namely 1-((8-hydroxyquinolin-5-yl)methyl)-3-methylthiourea (HQMT) and 5-isothiocyanatomethyl-8-hydroxyquinoline (TCHQ) were synthesized and identified by various spectroscopic methods (IR, NMR and Elemental analysis)
M. Faydy +6 more
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Two new 8-hydroxyquinoline derivatives namely 1-((8-hydroxyquinolin-5-yl)methyl)-3-methylthiourea (HQMT) and 5-isothiocyanatomethyl-8-hydroxyquinoline (TCHQ) were synthesized and identified by various spectroscopic methods (IR, NMR and Elemental analysis)
M. Faydy +6 more
semanticscholar +1 more source

