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On 8-Hydroxyquinoline-Zinc Oxide Incompatibility

Dermatology, 1974
Although it is well known that zinc ions and the oxines form practically insoluble chelates, oxines are commonly used in combination with zinc oxide in ointment form. 13 patients who had shown allergic responses after epicutaneous testing with oxines were tested with iodochloroxine and certain combinations of it with starch, titanium dioxide and zinc ...
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Chelating resins from 8-hydroxyquinoline

Analytica Chimica Acta, 1974
Abstract The preparation and properties of chelating resins containing the oxine group have been studied. Condensation resins with the optimal swelling properties were made by control of the water content during curing. The resins have high capacity and selectivity, and a fast exchange rate resulted from the incorporation of a proportion of sulphonic
J.R. Parrish, R. Stevenson
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8-Hydroxyquinolines in metallosupramolecular chemistry

Coordination Chemistry Reviews, 2008
8-Hydroxyquinoline is a versatile ligand in coordination chemistry which was mainly used for analytical purposes. Due to the special properties of some of its complexes it experienced a renaissance in synthetic coordination chemistry. This review describes recent applications of 8-hydroxyquinoline derivatives to obtain new supramolecular sensors ...
Markus Albrecht   +2 more
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Photoemission study of tris(8-hydroxyquinoline) aluminum/aluminum oxide/tris(8-hydroxyquinoline) aluminum interface

Journal of Applied Physics, 2006
The evolution of the interface electronic structure of a sandwich structure involving aluminum oxide and tris(8-hydroxyquinoline) aluminum (Alq), i.e., (Alq∕AlOx∕Alq), has been investigated with photoemission spectroscopy. Strong chemical reactions have been observed due to aluminum deposition onto the Alq substrate.
Huanjun Ding   +4 more
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Spectrophotometric determination of halogenated 8-hydroxyquinoline derivatives

Talanta, 1984
A spectrophotometric method is proposed for the determination of 8-hydroxyquinoline and three of its iodinated derivatives: 5-chloro-7-iodo-8-hydroxyquinoline (clioquinol), 5,7-di-iodo-8-hydroxy-quinoline (iodoquinol) and 8-hydroxy-7-iodo-quinolone-5-sulphonic acid (chinoform).
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8‐Hydroxyquinolinate of Quadripositive Praseodymium

Journal of the Chinese Chemical Society, 1955
AbstractGreenish yellow Pr(C9H6NO)4·H2O has been prepared in the same manner as the 8‐hydroxyquinolinate of quadripositive neodymium(1). The quadrivalence of praseodymium has been confirmed bromometrically, 15 bromine atoms being needed to brominate one molecule of the substance.Yellow Pr(C9H6NO)3 · H2O has also been prepared by the addition of ...
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8-HYDROXYQUINOLINES

1978
J. STARY, H. FREISER
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THE HALOGENATED 8‐HYDROXYQUINOLINES

International Journal of Dermatology, 1977
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