Absolute configuration assignment in racemic trans-stilbene oxide using chiral liquid chromatography with combined chiroptical detection and time-dependent density functional theory calculations

• JUAN P CASTILLO-GONZÁLEZ ^[1] ; NATALIA I GONZÁLEZ-PEÑA ^[1] ; MARCELO A MUÑOZ ^[1]
  1. [1] Universidad Austral de Chile

     Universidad Austral de Chile

     Valdivia, Chile

     
• Localización: Journal of the Chilean Chemical Society (Boletín de la Sociedad Chilena de Química), ISSN-e 0717-6309, ISSN 0366-1644, Vol. 61, Nº. 1, 2016, págs. 2777-2779
• Idioma: inglés
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• Resumen

  • A chiral chromatographic analysis using HPLC coupled in series with circular dichroism and optical rotation detectors (HPLC-CD-OR) was applied to racemic trans-stilbene oxide, allowing the on-line measurement of the CD spectra and [α] values for both enantiomers in the sample. These measurementsused the Gaussian peak model to estimate the concentration of each isomer in the CD and OR cells. Moreover, time-dependent density functional theory (TD-DFT) calculations at the B3LYP/TZVP//B3LYP/VDZ(P) and B3LYP/aug-cc-pVDZ//B3LYP/VDZ(P) levels of the ory for CD and OR, respectively, permitted the prediction of both chiroptical properties for each isomer, which in turn could be compared with the corresponding experimental data. In this case, the calculationswere consistent in predicting the correct combination of experimental CD bands and [a] sign and the refore facilitated the absolute configuration (AC) assignment of the optical isomers. The AC proposed using this methodology was in agreement with independent AC assignments in the literature.