Add time:07/26/2019 Source:sciencedirect.com
The crystal and molecular structures of methyl (N-benzoylaminooxy)acetate (MBAOA) have been determined by X-ray diffraction at room temperature. In the crystal the amide CO of one molecule is hydrogen-bonded to the amide NH of an adjacent molecule (O1 ⋯ N1′ = 2.850(2) Å, O1 ⋯ H6′N1′ = 158(2)°). The ester CO bond is cis oriented to the CO (aminooxy) bond (the O2-C8-C0-O4 torsion angle is 2.6(3)°). IR and Raman spectra of MBAOA and its deuterated analogs have been measured in the solid state and in solution. In polar solvents the ester vCO was observed as a doublet feature in IR spectra, suggesting the existence of the two conformers having different torsion angles around the (O)CC(=O) bond. By combining the X-ray crystallographic result with the IR and Raman data, it is suggested that the conformer with the higher frequency of the ester vCO in solution has the ester CO bond cis oriented to the CO (aminooxy) bond.
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