Pregled bibliografske jedinice broj: 134327
Kinetics and Mechanism of the Rections of Aquapentacyanofe(II) Ions with the Biologically Active Bis-pyridinium aldoxime (TMB-4)
Kinetics and Mechanism of the Rections of Aquapentacyanofe(II) Ions with the Biologically Active Bis-pyridinium aldoxime (TMB-4) // Book of Abstracts: 1st Central European Conference "Chemistry towards Biology" / Kaučič V., Mali G. (ur.).
Ljubljana: Slovenian Chemical Society, 2002. str. 73-73 (poster, međunarodna recenzija, sažetak, znanstveni)
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Naslov
Kinetics and Mechanism of the Rections of Aquapentacyanofe(II) Ions with the Biologically Active Bis-pyridinium aldoxime (TMB-4)
Autori
Foretić, Blaženka ; Pogledić, Ivana ; Burger, Nicoletta
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Book of Abstracts: 1st Central European Conference "Chemistry towards Biology"
/ Kaučič V., Mali G. - Ljubljana : Slovenian Chemical Society, 2002, 73-73
Skup
1st Central European Conference "Chemistry towards Biology"
Mjesto i datum
Portorož, Slovenija, 08.09.2002. - 12.09.2002
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
1; 1’; -Bis(pyridinium-4-aldoxime)trimethylene dibromide; Aquapentacyanoferrate(II); Kinetics
Sažetak
It is well known that mono- and bis-quaternary pyridinium aldoximes are potent reactivators of the acetylcholinesterase activity inhibited by organophosphates. One of the representative of the bis-pyridinium class is the 1, 1'-bis(pyridinium-4-aldoxime)trimethylene dibromide (TMB-4). TMB-4 reacts with aquapentacyanoferrate(II) ions forming a blue pentacyanoferrate(II) complex. The kinetics of the substitution reactions of the aquapentacyanoferrate(II) ions with TMB-4 were studied in aqueous media in the range pH 5-11, I=0.50 M and 25 C. The rates of the formation and dissociation of the TMB-4 substituted pentacyanoferrate(II) was found to be pH dependent, which is attributed to the reactions of various ionic forms of the ligand. The relationships between the formation rate constants and the magnitude and position of charges on the ligand and its various possible configurations and conformations are discussed in terms of an ion-pair dissociative mechanism.
Izvorni jezik
Engleski
Znanstvena područja
Kemija