Rate constants and activation parameters for the isotopic exchange reactions between (Ph0)2PSCl and M:Wl (M = MedN+, Et4N+, n-BudN+, Et,,HN+, EtH:,N+, Li+) in acetonitrile were measured in order to find the effect of the cation nature on the kinetics of the reaction. T h e rate constants measured fo
The kinetics of the chlorine isotopic exchange between chloride ion at O,O-diarylphosphorochloridates or O,O-diarylphosphorochloridothionates
✍ Scribed by W. ReimschüSsel; M. Mikołajczyk; H. Ślebocka-tilk; M. Gajl
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 535 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0538-8066
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✦ Synopsis
The kinetics of the chlorine isotopic exchange reaction between tetraethylammonium ~hloride-3~Cl and 0,O-diarylphosphorochloridates ( p -RCsH40)2POC1 or 0,O-diarylphosphorochloridothionates (p-RCsH40)2PSCl has been studied in acetonitrile solution. Good Hammett's correlations of the rate constants with Taft's u" constants were obtained. The values of the reaction constants p were found identical for phosphoryl and thiophosphoryl compounds. In comparison with oxygen in the phosphoryl group, the sulfur atom exhibits an electron-donating effect (Ago N 0.80). No correlation has been found for the enthalpg and entropy of activation. The effect of the substituents aryloxy groups, oxygen, or sulfur atoms in the phosphoryl group on the kinetics of the sN2-P reaction is discussed. The reactivity of the investigated compounds is determined by the extent of the positive charge localized on the phosphorus atom. The positive charge is formed by the direct interactions of the substituents with the reaction center and the indirect-intramolecular interactions revealed in the structure of the compound.
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