77887-35-5Relevant academic research and scientific papers
Dediazoniations of Arenediazonium Ions in Homogeneous Solutions. Part XVI. Kinetics and Mechanisms of Dediazoniation of p-Chlorobenzenediazonium Tetrafluorobarate in Weakly Alkaline Aqueous Solutions under Nitrogen Gas
Schwarz, Wolfgang,Zollinger, Heinrich
, p. 513 - 528 (1981)
The kinetics of reactions of p-chlorobenzenediazonium ions in aqueous buffer solutions (pH 9.0-10.6) under N2 (5 ppb of O2) have been measured between 20 and 50 deg C.The formation of trans-diazotate is first-order with respect to the concentration of hy
Kinetics and Intermediates in the Several Forward and Reverse Reactions of Nitro-substituted Arenediazonium Ions with Hydroxide Ion
Goodman, Paul D.,Kemp, Terence J.,Moira, Peter Pinot de
, p. 1221 - 1229 (2007/10/02)
Stopped- and quenched-flow kinetics and rapid-scanning u.v. spectrophotometry have been applied to the kinetics of the forward and reverse reactions of ArN2(1+) with OH(1-), where Ar bears one or more strongly electronegative substituents (Cl,NO2), in which case the syn-diazotate (formed rapidly from the initially produced diazohydroxyde) functions as a reactive intermediate leading to the thermodinamically favoured anti-diazotate.Measurements of forward and reverse rates in some cases have enabled the determination of equilibrium constants for both acid-base andisomerisation reactions.It has thus been possible to extend the number of compounds for which these data are available, and hence derive more complete linear free energy relationships for both kinetic and equlibrium constants. (These include determinations of Σ and ?+ parameters for the 2-nitro- and 2-chloro-groups.) A complete description of the quenched-flow apparatus is provided.Time-resolved u.v.-visible spectra of the transient syn-diazotate have been obtained for the 4-nitro, 2-chloro-4-nitro-, 4-chloro-2-nitro-, and 2,4-dinitro-substituted materials.
