The previous post looked at anomeric effects set up on centres such as B, Si or P, and involving two oxygen groups attached to these atoms. Here I vary the attached groups to include either one or two nitrogen atoms.[1]
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The plot below shows aminols, C(NHR)(OR”). A torsion along either the C-O or C-N bond of ~60° implies that (at two coordinate oxygen or three coordinated nitrogen) there may be a lone pair with a torsion of 180°, which would set up an antiperiplanar alignment between that lone pair and the adjacent C-O or C-N bond (the anomeric effect). The clear hotspot is at angles of ~80°, which does raise the issue of why it deviates from 60°. Only a location of the lone pair centroid (using eg the ELF quantum mechanical technique) would cast light on that. There is a less distinct region for which the C-N torsion is 60° and the C-O torsion 180°, and an even less distinct region for the reverse (C-O torsion is 60° and the C-N torsion 180°). This tends to imply that a nitrogen lone pair is a better donor into a C-O bond than the reverse. Electronegativity suggests this should indeed be so, with the N lone pair less bound by the N nucleus and hence easier to release into a C-Oσ* orbital which is a better acceptor than then equivalent C-Nσ* orbital.
Searches like this seem to be good at creating more questions than they answer. Clearly, the origins of the various hotspots need to be investigated, ideally using quantum mechanics to quantify the stereoelectronic interactions involved. So this sort of (ten minute) exercise is very good at raising research project investigations.
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