
Journal of the American Chemical Society p. 1162 - 1167 (1988)
Update date:2022-07-30
Topics:
Collins
Keech
In this report we discuss the first mechanistic study of facile isomerizations of diastereomeric complexes in which planar and nonplanar amido-N ligands are interconverted. The accumulated evidence consistently suggests that the T mechanism most reasonably describes the isomerizations of the systems studied. While the focus here has been upon processes occurring at a transition-metal center, the isomerization reactions interconvert cis- alpha and trans diastereomers where the enthalpy difference is primarily a result of the presence of nonplanar amido-N ligands in the former and planar amido-N ligands in the latter.
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