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Reactions of O ‐aryl S ‐aryl dithiocarbonates with pyridines in aqueous ethanol: kinetics and mechanism
Author(s) -
Castro Enrique A.,
Gazitúa Marcela,
Santos José G.
Publication year - 2009
Publication title -
journal of physical organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.325
H-Index - 66
eISSN - 1099-1395
pISSN - 0894-3230
DOI - 10.1002/poc.1553
Subject(s) - chemistry , aryl , kinetics , ethanol , aqueous solution , mechanism (biology) , organic chemistry , medicinal chemistry , alkyl , philosophy , epistemology , physics , quantum mechanics
The reactions of O ‐(4‐methylphenyl) S ‐(4‐nitrophenyl) dithiocarbonate ( 1 ), O ‐(4‐chlorophenyl) S ‐(4‐nitrophenyl) dithiocarbonate ( 2 ), and O ‐(4‐chlorophenyl) S ‐phenyl) dithiocarbonate ( 3 ) with a series of pyridines were subjected to a kinetic investigation in 44 wt% ethanol–water, at 25.0 °C and an ionic strength of 0.2 M. The reactions were followed spectrophotometrically. Under amine excess, pseudo‐first‐order rate coefficients ( k obs ) were determined. For the studied reactions, plots of k obs versus free pyridine concentration at constant pH were linear, with the slope ( k N ) independent of pH. The Brønsted‐type plots for ( 1 ) and ( 2 ) were biphasic, suggesting a stepwise mechanism with a change in the rate‐determining step, from breakdown to the formation of a tetrahedral intermediate (T ± ), as the basicity of the pyridines increases. For the reactions of ( 3 ), at the p K a range of the pyridines studied, only the breakdown to products of T ± was observed. Copyright © 2009 John Wiley & Sons, Ltd.