1 |
Merenyi G, Lind JS. Role of a peroxide intermediate in the chemiluminescence of luminal: a mechanistic study. J. Am. Chem. Soc. 1980;102:5830-5835.
DOI
|
2 |
Nosaka Y, Yamashita Y, Fukuyama H. Application of chemiluminescent probe to monitoring superoxide radicals and hydrogen peroxide in photocatalysis. J. Phys. Chem. B 1997;101:5822-5827.
DOI
ScienceOn
|
3 |
Naguib YM. A fluorometric method for measurement of peroxyl radical scavenging activities of lipophilic antioxidants. Anal. Biochem. 1998;265:290-298.
DOI
ScienceOn
|
4 |
Armstrong WA, Black BA, Grant DW. The radiolysis of aqueous calcium benzoate and benzoic acid solutions. J. Phys. Chem. 1960;64:1415-1419.
DOI
|
5 |
Klein GW, Bhatia K, Madhavan V, Schuler RH. Reaction of hydroxyl radicals with benzoic acid: isomer distribution in the radical intermediates. J. Phys. Chem. 1975;79:1767-1774.
DOI
|
6 |
Oturan MA, Pinson J. Hydroxylation by electrochemically generated OH radicals. Mono- and polyhydroxylation of benzoic acid: products and isomer distribution. J. Phys. Chem. 1995;99:13948-13954.
DOI
ScienceOn
|
7 |
Mason TJ, Lorimer JP, Bates DM, Zhao Y. Dosimetry in sonochemistry: the use of aqueous terephthalate ion as a fluorescence monitor. Ultrason. Sonochem. 1994;1:S91-S95.
DOI
ScienceOn
|
8 |
Ishibashi K, Fujishima A, Watanabe T, Hashimoto K. Quantum yields of active oxidative species formed on photocatalyst. J. Photochem. Photobiol. A Chem. 2000;134:139-142.
DOI
ScienceOn
|
9 |
Fang X, Mark G, von Sonntag C. OH radical formation by ultrasound in aqueous solutions. Part I: the chemistry underlying the terephthalate dosimeter. Ultrason. Sonochem. 1996;3:57-63.
DOI
ScienceOn
|
10 |
Czapski G, Bielski BH. The formation and decay of and in electron-irradiated aqueous solutions. J. Phys. Chem. 1963;67:2180-2184.
DOI
|
11 |
Schwartz SE. Gas- and aqueous-phase chemistry of in liquid water clouds. J. Geophys. Res. 1984;89:11589-11598.
DOI
|
12 |
Sander R. Compilation of Henry's law constants for inorganic and organic species of potential importance in environmental chemistry. Mainz: Max-Planck Institute of Chemistry; 1999.
|
13 |
Seinfeld JH, Pandis SN. Atmospheric chemistry and physics: from air pollution to climate change. New York: Wiley; 1998.
|
14 |
Kwon BG, Kim E, Lee JH. Pentachlorophenol decomposition by electron beam process enhanced in the presence of Fe(III)-EDTA. Chemosphere 2009;74:1335-1339.
DOI
ScienceOn
|
15 |
Sawyer DT, Valentine JS. How super is superoxide? Acc. Chem. Res. 1981;14:393-400.
DOI
|
16 |
Staehelin J, Hoigne J. Decomposition of ozone in water: rate of initiation by hydroxide ions and hydrogen peroxide. Environ. Sci. Technol. 1982;16:676-681.
DOI
ScienceOn
|
17 |
Bielski BH, Cabelli DE, Arudi RL. Reactivity of - radical in aqueous solution. J. Phys. Chem. Ref. Data 1985;14:1041- 1100.
DOI
|
18 |
von Sonntag C, Dowideit P, Fang X, et al. The fate of peroxyl radicals in aqueous solution. Water Sci. Technol. 1997;35:9- 15.
|
19 |
Kwon BG, Lee JH. A kinetic method for - determination in advanced oxidation processes. Anal. Chem. 2004;76:6359-6364.
DOI
ScienceOn
|
20 |
Kwon BG, Yoon J. Experimental evidence of the mobility of hydroperoxyl/superoxide anion radicals from the illuminated interface into the aqueous phase. Bull. Korean Chem. Soc. 2009;30:667-670.
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DOI
ScienceOn
|
21 |
Buxton GV, Greenstock CL, Helman WP, Ross AB. Critical review of rate constants for reactions of hydrated electrons, hydrogen atoms and hydroxyl radicals (.OH/. in aqueous solution. J. Phys. Chem. Ref. Data 1988;17:513-886.
DOI
|
22 |
Stefan MI, Hoy AR, Bolton JR. Kinetics and mechanism of the degradation and mineralization of acetone in dilute aqueous solution sensitized by the UV photolysis of hydrogen peroxide. Environ. Sci. Technol. 1996;30:2382-2390.
DOI
ScienceOn
|
23 |
Goldstein S, Lind J, Merenyi G. Chemistry of peroxynitrites as compared to peroxynitrates. Chem. Rev. 2005;105:2457-2470.
DOI
ScienceOn
|
24 |
Butler J, Halliwell B. Reaction of iron-EDTA chelates with the superoxide radical. Arch. Biochem. Biophys. 1982;218:174- 178.
DOI
ScienceOn
|
25 |
Kwon BG, Kim JO, Namkung KC. The formation of reactive species having hydroxyl radical-like reactivity from UV photolysis of N-nitrosodimethylamine (NDMA): kinetics and mechanism. Sci. Total Environ. 2012;437:237-244.
DOI
ScienceOn
|
26 |
Fridovich I. Quantitative aspects of the production of superoxide anion radical by milk xanthine oxidase. J. Biol. Chem. 1970;245:4053-4057.
|
27 |
Fridovich I. Superoxide radical and superoxide dismutase. Acc. Chem. Res. 1972;5:321-326.
DOI
|
28 |
Halliwell B. Antioxidant characterization: methodology and mechanism. Biochem. Pharmacol. 1995;49:1341-1348.
DOI
ScienceOn
|
29 |
Bhattacharya D, Maji S, Pal K, Sarkar S. Formation of superoxide anion on aerial oxidation of Cu(II)-porphyrinogen in the synthesis of tetrakis(cyclohexyl)porphyrinogenCu(III) anion. Inorg. Chem. 2008;47:5036-5038.
DOI
ScienceOn
|
30 |
McDowell MS, Bakac A, Espenson JH. A convenient route to superoxide ion in aqueous solution. Inorg. Chem. 1983;22:847-848.
DOI
|
31 |
Schwarz HA. Free radicals generated by radiolysis of aqueous solutions. J. Chem. Educ. 1981;58:101-105.
DOI
|
32 |
Okado-Matsumoto A, Fridovich I. Assay of superoxide dismutase: cautions relevant to the use of cytochrome c, a sulfonated tetrazolium, and cyanide. Anal. Biochem. 2001;298:337- 342.
DOI
ScienceOn
|
33 |
Flyunt R, Leitzke A, Mark G, et al. Determination of .OH, , and hydroperoxide yields in ozone reactions in aqueous solution. J. Phys. Chem. B 2003;107:7242-7253.
DOI
ScienceOn
|