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Gasparrini F, Pierini M, Villani C, et al. Enantiomerization study of some alpha-nitroketones by dynamic high-resolution gas chromatography. J Org Chem. 2003;68(8):3173-7doi: 10.1021/jo0267302.
Gasparrini, F., Pierini, M., Villani, C., De Maria, P., Fontana, A., & Ballini, R. (2003). Enantiomerization study of some alpha-nitroketones by dynamic high-resolution gas chromatography. The Journal of organic chemistry, 68(8), 3173-7. https://doi.org/10.1021/jo0267302
Gasparrini, Francesco, et al. "Enantiomerization study of some alpha-nitroketones by dynamic high-resolution gas chromatography." The Journal of organic chemistry vol. 68,8 (2003): 3173-7. doi: https://doi.org/10.1021/jo0267302
Gasparrini F, Pierini M, Villani C, De Maria P, Fontana A, Ballini R. Enantiomerization study of some alpha-nitroketones by dynamic high-resolution gas chromatography. J Org Chem. 2003 Apr 18;68(8):3173-7. doi: 10.1021/jo0267302. PMID: 12688787.
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J Org Chem. 2003 Apr 18;68(8):3173-7. doi: 10.1021/jo0267302.

Enantiomerization study of some alpha-nitroketones by dynamic high-resolution gas chromatography.

The Journal of organic chemistry

Francesco Gasparrini, Marco Pierini, Claudio Villani, Paolo De Maria, Antonella Fontana, Roberto Ballini

Affiliations

  1. Dipartimento di Studi di Chimica e Tecnologia delle Sostanze Biologicamente Attive, Università La Sapienza, Piazzale A. Moro 5, 00185 Rome, Italy. [email protected]

PMID: 12688787 DOI: 10.1021/jo0267302

Abstract

The kinetics of the reversible enantiomer interconversion of 3-nitrobutan-2-one (1), 3-nitropentan-2-one (2), and 2-nitropentan-3-one (3) have been studied by dynamic high-resolution gas chromatography (DHRGC) by using a beta-cyclodextrin derivative chiral stationary phase; the process occurs via enolization of the keto forms. The DHRGC experiments involving the studied nitroketones and the chiral stationary phase show chromatographic profiles with a typical interconversion plateau in the temperature range between 130 and 160 degrees C. Computer simulation of the experimental chromatographic elution profiles was employed for the determination of rate constants and the corresponding enantiomerization barriers (k, DeltaG#(T), DeltaH#, and DeltaS#). The highly negative entropy of activation (DeltaS# values from -19 to -37 cal mol(-1) K(-1)) points to a transition state (TS) with large charge separation. The obtained results for 1-3 show the dramatic effect of an alpha-nitro-substituent on the rate of enolization of simple ketones, when compared with those for 3-chloro-2-butanone and 3-methyl-2-pentanone. To get some information on the separate contributions of the stationary liquid phase and the mobile gas phase on the studied process, some DFT ab initio calculations have been performed for the same compounds.

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