Structure and Dynamics of Phosphorus(V)-Stabilized Carbanions: A Comparison of Theoretical, Crystallographic, and Solution Structures
Cramer, C. J.; Denmark, S. E.; Miller, P. C.; Dorow, R. L.; Swiss, K. A.;
Wilson, S. R.
J. Am. Chem. Soc. 1994, 116, 2437.
The rotational coordinates about the P-C bond in four different phosphorus(V)-substituted methyl anions have been studied in detail at the HF/3-21G(*) level, with stationary points characterized at levels equivalent to MP3/6-31+G*//HF/6-31+G*. The locations of local minima on the rotational coordinate were found to be dependent on opportunities for hyperconjugative stabilization. When amino substituents on phosphorus were geometrically unconstrained, two local minima were found. By contrast, when the amino groups were constrained to local geometries similar to those found in diazaphosphorinanes, the effects on the rotation coordinate were considerable. A single minimum and a higher rotation barrier were noted. Comparisons of static structure and rotational dynamics are made to both solution and solid phase experimental data. The single crystal X-ray structure of lithio-N,N,N',N'-tetramethyl-P-benzylphosphondiamide (7) is reported.
To request a copy of this article, send e-mail to the Research Reports Coordinator at the Minnesota Supercomputer Institute (firstname.lastname@example.org). Please provide a mailing address and specify that you would like UMSI report 94/9.