Pregled bibliografske jedinice broj: 1080111
Reductive iodide elimination from iodophenols by alcohol derived radicals; chain reaction induced by proton-coupled electron transfer
Reductive iodide elimination from iodophenols by alcohol derived radicals; chain reaction induced by proton-coupled electron transfer // 3rd European Young Investigator Conference EYIC '07
Słubice, Poljska, 2007. str. P3-P3 (poster, podatak o recenziji nije dostupan, sažetak, znanstveni)
CROSBI ID: 1080111 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Reductive iodide elimination from iodophenols
by alcohol derived radicals; chain reaction
induced by proton-coupled electron transfer
Autori
Matasović, Brunislav ; Bonifačić, Marija
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
3rd European Young Investigator Conference EYIC '07
/ - , 2007, P3-P3
Skup
3rd European Young Investigator Conference EYIC '07
Mjesto i datum
Słubice, Poljska, 13.06.2007. - 16.06.2007
Vrsta sudjelovanja
Poster
Vrsta recenzije
Podatak o recenziji nije dostupan
Ključne riječi
PCET mechanism ; Chain reactions ; Rate constant ; Dehalogation
Sažetak
Gamma-Radiolysis and measurements of iodide by means of ion chromatography have been employed to investigate reductive dehalogenation of iodophenols by carbon-centered radicals, .CH(CH3)OH, .CH2OH, and .CO2-, in oxygen free neutral aqueous solutions in the presence of ethanol, methanol or sodium formate. While the reaction of 4-IC6H4OH with .CH(CH3)OH of .CH2OH radicals is endothermic in water/alcohol solutions, addition of bicarbonate leads to iodide production in high yields indicative for a chain reaction. No such effect was observed with phosphate, a buffer with higher proton affinity. Formation of a complex between alpha- hydroxy alcohol radicals and the bicarbonate anion is proposed enhancing the reduction power of the former to the extentthat the electron transfer to iodophenol meolecule becomes exothermic. This indicates one-electron reduction reactions by alpha-hydroxy alkyl radicals to occur by the concerted proton- coupled electron transfer and not by a two step ET/PT or PT/ET mechanism. Reduction power of the carbonate radical anion is shown to be high enough to reduce iodophenols by the one- electron transfer mechanism. In the presence of formate ions as an H-atom donor, dehalogenation also occurs by a chain reaction. In all systems the chain lenghts were dependent on the rate of reductive radicals reproduction in the propagation step, i.e. the H-atom abstraction from methanol, ethanol or formate by 4-.C6H4OH radicals. The rate constant of this reaction was determined from the iodide yield measurements at constant irradiation dose rate and was estimated to be 6 M-1 s-1 for methanol, 140 M-1 s-1 for ethanol and 2100 M-1 s-1 for formate. Results will be discussed in view of their significance for the environmental remediation.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
098-0982915-2949 - Površinski aktivne tvari, procesi u otopinama i na međupovršinama (Dutour Sikirić, Maja, MZOS ) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb