Literature DB >> 12610991

On the kinetics and energetics of one-electron oxidation of 1,3,5-triazines.

M E D G Azenha1, H D Burrows, M Canle, R Coimbra, M I Fernández, M V García, A E Rodrigues, J A Santaballa, S Steenken.   

Abstract

One-electron oxidation of 1,3,5-triazines is observed with both excited uranyl ion (*UO2(2+)) and sulfate radical anion (SO4.-) in aqueous solution, but not with Tl2+, indicating that the standard reduction potentials E degree of 1,3,5-triazine radical cations are = 2.3 +/- 0.1 V vs. NHE, consistent with theoretical calculations; this suggests that if triazines inhibit electron transfer during photosynthesis, they would need to act on the reductive part of the electron transport chain.

Entities:  

Year:  2003        PMID: 12610991     DOI: 10.1039/b210119j

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  Synthesis of 2,4,6-tri-substituted-1,3,5-triazines.

Authors:  Carlos A M Afonso; Nuno M T Lourenço; Andreia de A Rosatella
Journal:  Molecules       Date:  2006-01-31       Impact factor: 4.411

2.  Influence of solution pH on degradation of atrazine during UV and UV/H2O2 oxidation: kinetics, mechanism, and degradation pathways.

Authors:  Yucan Liu; Kai Zhu; Miaomiao Su; Huayu Zhu; Jianbo Lu; Yuxia Wang; Jinkun Dong; Hao Qin; Ying Wang; Yan Zhang
Journal:  RSC Adv       Date:  2019-11-04       Impact factor: 4.036

  2 in total

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