AbstractHigh-resolution rotational spectroscopy was used to investigate the conformational landscape of methyl-3,3,3-trifluoropyruvate, a small, partially-fluorinated molecule, which is of interest because of its chemical properties and reactivity in contrast to the unfluorinated species. Methyl 3,3,3-trifluoropyruvate is also subject to two possible large amplitude motions of the methyl and trifluoromethyl group. However, only the methyl rotor gives rise to the tunneling splitting specific to individual conformers. In the rotational spectrum measured in the frequency region from 6 to 27 GHz, the identified conformers, s-cis and s-trans, were fitted to experimental accuracy, resulting in the accurate determination of the vibrational ground state rotational constants ${A}_{0}=2185.05827\left(36\right)\text{\hspace{0.17em}MHz}$, ${B}_{0}=1023.30031\left(17\right)\text{\hspace{0.17em}MHz}$, and ${C}_{0}=803.520287\left(95\right)\text{\hspace{0.17em}MHz}$ for the s-cis conformer, and ${A}_{0}=2706.9024\left(49\right)\text{\hspace{0.17em}MHz}$, ${B}_{0}=864.889539\left(81\right)\text{\hspace{0.17em}MHz}$, and ${C}_{0}=746.532896\left(71\right)\text{\hspace{0.17em}MHz}$ for the s-trans conformer. Additionally the barrier heights of the methyl rotor ${V}_{3}\left({\text{CH}}_{3}\right)=363.116\left(94\right){\text{\hspace{0.17em}cm}}^{-1}$ and ${V}_{3}\left({\text{CH}}_{3}\right)=389.290\left(80\right){\text{\hspace{0.17em}cm}}^{-1}$ were obtained for the s-cis and s-trans conformer, respectively.
Targeting the Rich Conformational Landscape of
N
‐Allylmethylamine Using Rotational Spectroscopy and Quantum Mechanical Calculations
