Damodaran, K and Nielsen, SD and Geib, SJ and Zhang, W and Lu, Y and Curran, DP
(2009)
Aryl-Csp<sup>3</sup> bond rotation barriers of 2-aryl perhydropyrrolo[3,4- c]pyrrole-1,3-diones.
Journal of Organic Chemistry, 74 (15).
5481 - 5485.
ISSN 0022-3263
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Abstract
(Chemical Equation Presented) The static and dynamic features of 2-aryl perhydropyrrolo[3,4-c]pyrrole-1,3-diones bearing N-acyl substituents have been assessed with the aid of crystal structures and VT NMR spectra. Rotation barriers for the aryl-Csp3 bonds in these molecules show surprising variation. Amide-substituted derivatives and fused piperazinediones (six-membered fusion) exhibit very substantial barriers of 14-15 kcal/mol. Fused benzodiazepinediones (seven-membered fusion) have lower but still significant barriers (10 kcal/mol), while fused hydantoins (five-membered fusion) have barriers that are too low to measure by VT NMR (≤10 kcal/mol). A rationale for the origin of the barriers is presented. © 2009 American Chemical Society.
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