Naslov
Solvolytic reactivity of pyridinium ions

Autori
Jurić, Sandra ; Kronja, Olga

Izvornik
Journal of physical organic chemistry (0894-3230) 28 (2015), 5; 314-319

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, ostalo

Ključne riječi
intrinsic barriers ; kinetics ; nucleofugality ; pyridinium ions ; solvolysis

Sažetak
The leaving group abilities of pyridine, 4-methylpyridine, and 4-chloropyridine in SN1 solvolytic reactions have been determined by analyzing the rate constants of X, Y-substituted benzhydrylpyridinium salts obtained in various solvents. By applying the linear free energy relationship equation, log k = sf (Ef + Nf), the nucleofuge specific parameters of 4-substituted pyridine have been extracted. Because of solvation in the reactant ground state, the reactivity (nucleofugality, Nf) of a given pyridine decreases as the polarity of the solvent increases. High slope parameters (sf>1) may be due to the spread of the energy levels of the benzhydrylium ion/pyridine pair intermediates in comparison to benzhydrylium ion/chloride pairs (sf≈1). Because of slow heterolysis step of pyridinium salts in various solvents, some are stable under normal conditions.

Izvorni jezik
Engleski

Znanstvena područja
Kemija

POVEZANOST RADA