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Investigation of novel radical scavenging mechanisms in the alkaline environment: Green, sustainable and environmentally friendly antioxidative agent(s)
被引:2
|作者:
Antonijevic, Marko
[1
,2
]
Avdovic, Edina
[2
]
Simijonovic, Dusica
[2
]
Milanovic, Ziko
[2
]
Zizic, Milan
[3
]
Markovic, Zoran
[2
,4
,5
]
机构:
[1] Univ Kragujevac, Fac Sci, Dept Chem, Radoja Domanovica 12, Kragujevac 34000, Serbia
[2] Univ Kragujevac, Inst Informat Technol, Dept Sci, Kragujevac 34000, Serbia
[3] Univ Belgrade, Inst Multidisciplinary Res, Life Sci Dept, Kneza Viseslava 1, Belgrade 11030, Serbia
[4] State Univ Novi Pazar, Dept Nat Sci & Math, Novi Pazar 36300, Serbia
[5] Univ Appl Sci, Dept Engn & Nat Sci, Eberhard Leibnitz Str 2, D-06217 Merseburg, Germany
关键词:
Hydroxyl radical;
Advanced oxidation processes;
Electron paramagnetic resonance;
Alkaline environment;
Coumarin;
DENSITY FUNCTIONALS;
2-STATE REACTIVITY;
DEPMPO;
M06;
D O I:
10.1016/j.scitotenv.2023.169307
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
Pharmaceutical and industrial utilization of synthetic chemicals has an immerse impact on the environment. In that sense, novel chemicals with potential for industrial application should be investigated for their behaviour in reactions with hydroxyl radical, simulating AOPs (Advanced Oxidation Processes). AOPs are known for being highly effective in wastewater management and natural water remediation. In this paper, exhaustive research on the radical scavenging activity of a newly synthesized coumarin derivative (4HCBH), as a representative of the series of coumarin-benzohydrazides with high antioxidative potential was conducted. This study took into consideration the pH value range significant for practically all living organisms (pH = 7.0-8.5). According to the experimentally obtained results, the 4HCBH showed an increase in radical scavenging activity, following the slight increase in pH values, which suggested that the formation of anionic form of 4HCBH is responsible for its antiradical activity. Further investigations led to the postulation of a novel mechanistic approach called Sequential Proton Loss Electron Transfer - Radical-Radical Coupling (SPLET-RRC), in which, by a series of steps, a new, stable compound was formed. Furthermore, it was demonstrated that the product generated through SPLET-RRC showed lower toxicity than the parent molecule.
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页数:13
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