Pregled bibliografske jedinice broj: 75595
Time-resolved Pulse Radiolysis Studies on the Free Radicals and Hydrated Electrons with Halogenated Phenols
Time-resolved Pulse Radiolysis Studies on the Free Radicals and Hydrated Electrons with Halogenated Phenols // Book of Abstracts / Mill, T. (ur.).
Chicago (IL): American Chemical Society (ACS), 2001. (predavanje, nije recenziran, sažetak, znanstveni)
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Naslov
Time-resolved Pulse Radiolysis Studies on the Free Radicals and Hydrated Electrons with Halogenated Phenols
Autori
Bonifačić, Marija ; Asmus, Klaus-Dieter ; Gray, Kimberly A.
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Book of Abstracts
/ Mill, T. - Chicago (IL) : American Chemical Society (ACS), 2001
Skup
222nd American Chemical Society National Meeting
Mjesto i datum
Chicago (IL), Sjedinjene Američke Države, 26.08.2001. - 30.08.2001
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Nije recenziran
Ključne riječi
halogenated phenols; dehalogenation; radicals; hydrated electron; protonation; reduction; rate constants; pulse radiolysis
Sažetak
Carbon-centered radicals (reducing and non-reducing) have been shown to react very fast with halogenated phenols, resulting in a transient adduct radical with distinct optical absorptions in the UV. These adduct radicals exist in equilibrium with the initial reaction partners. Earlier studies had failed to provide any evidence for this intermediate. The decay of the transient radical adduct is accelerated by protons and proton donors such as the halogenated phenol itself. Acceleration of the decay also occurs with increasing OH concentration, leaving an optimal pH window of 6 - 8 for direct observation of the transient. Dehalogenation appears to be prevented whenever the transient adduct is protonated. Proton acceptors, on the other hand, appear to facilitate dehalogenation. With certain radicals, such as a-hydroxyalkyl or CO2 radicals, chain processes can be initiated.
Izvorni jezik
Engleski