ISSN:
1042-7163
Keywords:
Chemistry
Source:
Wiley InterScience Backfile Collection 1832-2000
Topics:
Chemistry and Pharmacology
Notes:
Enolization of the phosphoryl group has been studied where Y = PPh3, CN, Ts, COOEt, CONEt2; R and R′ = Et, Bu, Ph, EtO, BuO, PhO; and X = Cl, Br, ClO4, BF4. It has been established that substances with are phosphaenols, but in substances with Y = CONEt2 the phosphoryl group cannot be enolized under any conditions. Phosphaenolization is favored by a high acidifying ability of the Y group, the ability of the X anion to stabilize the phosphaenolic form due to formation of a hydrogen bond OH…X with the anion, and a low electronegativity of R and R′ groups. To evaluate the acidifying ability of Y, this article defines specific σ- constants dependent on the number of substituents at the α-carbon atom: σCH3-, σCH2- and σCH-. Their sums characterize the enolization ability of the phosphoryl group. The enolic structure in the solid state is possible if ∑CHn- 〉 2. If this sum lies in the range of 2 〈 ∑CHn- 〈 2.6 the phosphoryl-phosphaenol tautomerism can be expected in appropriate solutions. Acidic properties of the investigated compounds in MeNO2 and EtOH (absolute) have been determined. Calculations of the acidity of the phosphoryl CH forms (A) and of the phosphaenol OH forms (B) have been carried out.
Additional Material:
7 Ill.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1002/hc.520020603
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