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Collect. Czech. Chem. Commun. 2002, 67, 429-438
https://doi.org/10.1135/cccc20020429

Ultraviolet Absorption Spectra and Dissociation Constants of Diamino-1,3,5-triazines

Rafael Pérez, Rafael Marín Galvín and José M. Rodríguez Mellado*

Departamento de Química Física y Termodinámica Aplicada, Facultad de Ciencias, Universidad de Córdoba, E-14004-Córdoba, Spain

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  • Moreno Maria T., Rodríguez-Amaro Rafael, Rodríguez Mellado Jose M., Mayén Manuel, Jiménez Guardeño Francisco: Imidazolinone and triazine herbicides in soils in relation to the complexes formed with Cu(II) ions. Comptes Rendus Chimie 2018, 21, 884. <https://doi.org/10.1016/j.crci.2018.05.007>
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  • Jastrzabek Konrad, Bednarek Przemyslaw, Kolesinska Beata, Kaminski Zbigniew J.: Bis(4,6‐dimethoxy‐1,3,5‐triazin‐2‐yl) Ether as Coupling Reagent for Peptide Synthesis. Chemistry & Biodiversity 2013, 10, 952. <https://doi.org/10.1002/cbdv.201200369>
  • Sokolová Romana, Degano Ilaria, Bulíčková Jana, Žabka Ján, Gál Miroslav, Ramešová Šárka: On the stability of the bioactive flavonoids quercetin and luteolin under oxygen-free conditions. Analytical & Bioanalytical Chemistry 2012, 402, 975. <https://doi.org/10.1007/s00216-011-5504-3>
  • Sun Xinbo, Cao Zhengbing, Sun Yuyu: N-Chloro-alkoxy-s-triazine-Based Antimicrobial Additives: Preparation, Characterization, and Antimicrobial and Biofilm-Controlling Functions. Ind. Eng. Chem. Res. 2009, 48, 607. <https://doi.org/10.1021/ie801110s>
  • Rodríguez Mellado J. M., Ruiz Montoya M., Galvín R. Marín: The Reduction of 2,6‐Dimethoxy‐4‐chloro‐1,3,5‐triazine on Mercury Electrodes in Aqueous Solutions in Relation with the Reduction of s‐Triazine Herbicides. Electroanalysis 2004, 16, 1972. <https://doi.org/10.1002/elan.200403043>
  • Pérez R., Marı́n Galvı́n R., Rodrı́guez Mellado J. M., Ruiz Montoya M.: On the Electroreduction Mechanism of 2-Chloro-4,6-diamino-1,3,5-triazine on Mercury Electrodes. J. Electrochem. Soc. 2003, 150, E389. <https://doi.org/10.1149/1.1590995>