Collect. Czech. Chem. Commun.
1967, 32, 757-773
https://doi.org/10.1135/cccc19670757
Komplexe des Uranyls mit phenolischen Liganden VIII. Potentiometrische Untersuchung der Uranylkomplexe mit p-Nitrophenol, 4-Nitrobenzcatechin, 2,3-Dihydroxynaphthalin, Alizarin S, Pyrogallolcarbonsäure, Pyrogallolsulfonsäure und mit dem Gemisch von Tiron und Sulfosalicylsäure
M. Bartušek
Crossref Cited-by Linking
- Schechtel Eugen, Dören René, Frerichs Hajo, Panthöfer Martin, Mondeshki Mihail, Tremel Wolfgang: Mixed Ligand Shell Formation upon Catechol Ligand Adsorption on Hydrophobic TiO2 Nanoparticles. Langmuir 2019, 35, 12518. <https://doi.org/10.1021/acs.langmuir.9b02496>
- Ali Nour Mohammad-Sadik, Amaniampong Prince Nana, Karam Ayman: Determination of optimal conditions for electrodeposition of Tin(II) in the presence of Alizarin Red S. Heliyon 2016, 2, e00212. <https://doi.org/10.1016/j.heliyon.2016.e00212>
- Tarafder Pranab Kumar, Mondal Rabin Kumar: A review on the complex forming ability of O-O′ type ligands with transition metals: introducing 2,3-dihydroxynaphthalene as a potential analytical reagent. Reviews in Analytical Chemistry 2011, 30. <https://doi.org/10.1515/revac.2011.016>
- Han Shu-ying, Ming Xin, Qi Zheng-chun, Sheng Dong, Lian Hong-zhen: Retention prediction and hydrophobicity estimation of weak acidic compounds by reversed-phase liquid chromatography using acetic and perchloric acids as ion suppressors. Anal Bioanal Chem 2010, 398, 2731. <https://doi.org/10.1007/s00216-010-4173-y>
- Schwarz Karin, Frankel E. N., German J. B.: Partition behaviour of antioxidative phenolic compounds in heterophasic systems. Fett/Lipid 1996, 98, 115. <https://doi.org/10.1002/lipi.19960980306>
- Hrdlička Aleš, Vrchlabský Milan: Complex equilibria of molybdenum(VI) with 2,3-dihydroxynaphthalene. Mikrochim Acta 1989, 98, 55. <https://doi.org/10.1007/BF01244517>
- El-Hendawy Ahmed M., Griffith William P., O'Mahoney Caroline A., Williams David J.: Complexes of naphthalene-2,3-diol (H2ND) with group VI and group VIII metals, and the X-ray crystal structure of cis-(NH4)2[Mo2O5(ND)2]·2H2O. Polyhedron 1989, 8, 519. <https://doi.org/10.1016/S0277-5387(00)80750-0>
- Tabushi Iwao, Kobuke Yoshiaki: Molecular Design of Specific Uranophiles. Israel Journal of Chemistry 1985, 25, 217. <https://doi.org/10.1002/ijch.198500034>
- Hoshino Hitoshi, Saitoh Tohru, Taketomi Hirofumi, Yotsuyanagi Takao, Watanabe Hiroto, Tachikawa Kohei: Micellar solubilization equilibria for some analytical reagents in aqueous non-ionic surfactant solutions. Analytica Chimica Acta 1983, 147, 339. <https://doi.org/10.1016/0003-2670(83)80101-9>
- Vespalec R., Neča J.: Behaviour of dihyroxynaphtalenes in a reversed-phase chromatographic system. Journal of Chromatography A 1983, 281, 35. <https://doi.org/10.1016/S0021-9673(01)87864-X>
- Popa Gr., Ciurea I. C., Dumitrescu N., Buburuzan D.: Anwendung von Gallacetophenon und Gallobenzophenon zur spektrophotometrischen Uran(VI)-bestimmung. Mikrochim Acta 1972, 60, 883. <https://doi.org/10.1007/BF01239154>