Pregled bibliografske jedinice broj: 574722
Kinetics of the oxidation of hydroxyurea with vanadium(V) ions in acidic aqueous solution
Kinetics of the oxidation of hydroxyurea with vanadium(V) ions in acidic aqueous solution // Reaction Kinetics Mechanisms and Catalysis, 105 (2012), 2; 223-232 doi:10.1007/s11144-011-0411-3 (međunarodna recenzija, članak, znanstveni)
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Naslov
Kinetics of the oxidation of hydroxyurea with vanadium(V) ions in acidic aqueous solution
Autori
Gabričević, Mario
Izvornik
Reaction Kinetics Mechanisms and Catalysis (1878-5190) 105
(2012), 2;
223-232
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
vanadate; hydroxyurea; redox; kinetics
Sažetak
Hydroxyurea (HU) effectively reduces vanadate (VO2 +) into vanadyl (VO2+) species in acidic aqueous solution acting as a two-electron donor. The reaction starts by the formation of a transient complex followed by an electron transfer process that includes the formation and subsequent fading out of a free radical, U• (U•≡H2N–C(=O)N(H)O•). The rate determining step of the redox reaction is the formation of a free radical either by the inner-sphere one-electron transfer within the formed VO2 +-complexes, or by an outer sphere one- electron transfer from VO2 +-complex to the second VO2 + ion. Assuming a rapid pre-equilibrium for the proton-transfer and complexation reactions, an inner-sphere electron transfer pathway has been proposed when HU is in excess. When VO2 + in excess, an additional reaction possibly proceeds through two outer-sphere electron-transfer pathways
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Temeljne medicinske znanosti, Farmacija
POVEZANOST RADA
Projekti:
006-0061247-0978 - Gastrin kao kofaktor unosa željeza u organizam. (Gabričević, Mario, MZOS ) ( CroRIS)
Ustanove:
Farmaceutsko-biokemijski fakultet, Zagreb
Profili:
Mario Gabričević
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus