Pregled bibliografske jedinice broj: 675658
Kinetic and computational study of the base promoted mechanism of N−benzoilethylpyridinium−4−aldoxime rearrangement.
Kinetic and computational study of the base promoted mechanism of N−benzoilethylpyridinium−4−aldoxime rearrangement. // XXIII Skup kemičara i kemijskih inžinjera / Hadžiev, Andrea ; Blažeković, Zdenko (ur.).
Zagreb: Hrvatsko društvo kemijskih inženjera i tehnologa (HDKI) ; Hrvatsko kemijsko drustvo, 2013. str. 174-174 (poster, domaća recenzija, sažetak, ostalo)
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Naslov
Kinetic and computational study of the base promoted mechanism of N−benzoilethylpyridinium−4−aldoxime rearrangement.
Autori
Picek, Igor ; Vianello, Robert ; Foretić, Blaženka
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, ostalo
Skup
XXIII Skup kemičara i kemijskih inžinjera
Mjesto i datum
Osijek, Hrvatska, 21.04.2014. - 24.04.2014
Vrsta sudjelovanja
Poster
Vrsta recenzije
Domaća recenzija
Ključne riječi
pyridine-oxime ether
Sažetak
Our last research revealed that N-benzoylethylpyridinium-4-aldoxime chloride (BEPA4-Cl) was subject to decomposition in alkaline media with the generation of phenyl vinyl ketone and pyridine-4-aldoxime.[1] In addition, BEPA4-Cl underwent rearrangement reaction in highly alkaline solutions with the formation of the corresponding O-alkylated pyridine-4-aldoxime ether which was successfully isolated and characterized.[2] In the present work, in order to elucidate the mechanism of BEPA4-Cl base induced transformations in aqueous alkaline solutions, we have combined the experimental results obtained by kinetic and NMR measurements with theoretical calculations. NMR analysis of buffered aqueous mixtures confirmed that phenyl vinyl ketone and pyridine-4-aldoxime were the sole products in the pH range 7.510.5, while the pyridine oxime ether was formed at pH above 10.5. The combined kinetic and computational studies have shown two important aspects of mechanism. First, that only the oximate form of BEPA4-Cl is susceptible to further ionization and consequent β-elimination. Second, that the formation of pyridine oxime ether proceeds via tandem β-elimination/Michael addition reactions where β-elimination is the rate determining process. The deduced kinetic and thermodynamic activation parameters at 25 C and I=0.1 M confirmed that there is no change in mechanism of β-elimination within the investigated pH range. [1] B. Foretić, I. Picek, V. Damjanović, D. Cvijanović, D. Milić, J. Mol. Struct. 1019 (2012) 196–205. [2] I. Picek, J. Plavec, P. Šket, N. Burger, B. Foretić, Neočekivana izomerizacija 1-benzoil-etilpiridinij-4-aldoksim-iona, XXII. Hrvatski skup kemičara i kemijskih inženjera - Knjiga sažetaka / V. Tomašić, K. Maduna Valkaj (ur.), Zagreb : HDKI ; HKD, 2011. 169-169.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
108-1193079-3070 - Kompleksi željeza i biološki aktivnih liganada (Foretić, Blaženka, MZOS ) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb,
Medicinski fakultet, Zagreb