Rotational Spectra and Conformational Analysis of Diethylsilane and Diethyldifluorosilane
Sean A. Peebles, Michal M. Serafin, Rebecca A. Peebles, Gamil A. Guirgis, Howard D. Stidham
Abstract
Sean A. Peebles, Michal M. Serafin, Rebecca A. Peebles, Gamil A. Guirgis, Howard D. Stidham
Abstract
The rotational spectra belonging to the (28)Si isotopologue for three conformers of diethyldifluorosilane (Et(2)SiF(2)) and three conformers of diethylsilane (Et(2)SiH(2)) have been measured between 4 and 17 GHz by using pulsed-jet Fourier-transform microwave spectroscopy. Rotational spectra for the gauche-gauche, trans-trans, and trans-gauche conformers were identified for both molecules, while the significantly higher energy gauche-gauche' conformer was not observed. Ab initio calculations at the MP2(Full)/6-311+G(2d,2p) and MP2(Full)/6-311+G(2df,2pd) levels for the fluorine and the hydrogen analogues, respectively, provided rotational constants, dipole moment components, and the relative energies of the conformers to assist in the spectral assignment. In both molecules, the gauche-gauche conformer was identified by the ab initio calculations as the most stable. Agreement of the ab initio rotational constants with those from experiment was at worst 5%, with most rotational constants being predicted to within 2%.
OpenAlex reports 5 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
The rotational spectra belonging to the (28)Si isotopologue for three conformers of diethyldifluorosilane (Et(2)SiF(2)) and three conformers of diethylsilane (Et(2)SiH(2)) have been measured between 4 and 17 GHz by using pulsed-jet Fourier-transform microwave spectroscopy. Rotational spectra for the gauche-gauche, trans-trans, and trans-gauche conformers were identified for both molecules, while the significantly higher energy gauche-gauche' conformer was not observed. Ab initio calculations at the MP2(Full)/6-311+G(2d,2p) and MP2(Full)/6-311+G(2df,2pd) levels for the fluorine and the hydrogen analogues, respectively, provided rotational constants, dipole moment components, and the relative energies of the conformers to assist in the spectral assignment. In both molecules, the gauche-gauche conformer was identified by the ab initio calculations as the most stable. Agreement of the ab initio rotational constants with those from experiment was at worst 5%, with most rotational constants being predicted to within 2%.
Key concepts: Conformational isomerism, Isotopologue, Rotational spectroscopy, Ab initio, Ab initio quantum chemistry methods, Dipole, Spectral line, Rotational–vibrational spectroscopy