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Chiral ureas with two electronegative substituents at 1‐N: An unusual case of coexisting pyramidal and almost planar 1‐N atoms in the same crystal
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Citations
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References
2008
Year
Crystal StructureElectronegative SubstituentsEngineeringXrd StudiesBiochemistryNatural SciencesChemical BondMolecular BiologyStructure ElucidationOrbital InteractionOrganic ChemistryPlanar ConfigurationSame CrystalChemistryChiral UreasCrystallographyCrystal Structure DesignBiophysics
XRD studies of structure of N-acetoxy-N-methoxyurea and N,N-bis(methoxycarbonyl)-N-methoxyimide have revealed that in N-methoxy-N-X-ureas (X = OAc, Cl, OMe, N(+)C(5)H(5)) the additional shortening of N-OMe bond took place, which arising from an n(O(Me))-sigma*(N-X) anomeric orbital interaction. XRD studies of N-chloro-N-ethoxyurea crystal have revealed the presence of two kinds of anomeric nitrogen configuration in the O-N-Cl group in the form of a pyramidal configuration and a planar configuration for same 1-N nitrogen atom. XRD studies of N-4-chlorobenzoyloxy-N-ethoxyurea have revealed that the degree of pyramidality of the 1-N nitrogen in N-aroyloxy-N-alkoxyureas is tuned by orientation of benzoyl group with respect to the N-O bond, which in turn depends of size of N-alkoxy group.
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