Vibrational Spectra, DFT Calculations, Unusual Structure, Anomalous CH2 Wagging and Twisting Modes, and Phase-Dependent Conformation of 1,3-Disilacyclobutane
Citations Over Time
Abstract
Our previously published infrared and Raman spectra of 1,3-disilacyclobutane (13DSCB) and its 1,1,3,3-d4 isotopomer have been reexamined and partially reassigned on the basis of DFT and ab initio calculations. The calculations confirm previous microwave work that the CSiC angles in the ring are unexpectedly larger than the SiCSi angles. This may arise from the partial charges on the ring atoms. The calculations are in excellent agreement with the observed spectra in both frequency and intensity. They also demonstrate that this molecule has CH2 wagging and twisting vibrations with frequencies below 1000 cm-1, about 200 cm-1 lower than expected. These unprecedented low values can be explained by the decreased slope in the potential energy curves for these vibrations as the sideways motions of the CH2 groups result in attractive forces between the positively charged hydrogens on the carbon atoms and the negatively charged hydrogens on the silicon atoms. The theoretical calculations also confirm the previous conclusions that the individual molecules (vapor) have C2v symmetry whereas in the solid the molecules become planar with D2h symmetry. The vibrational coupling between the ring-angle bending mode and the SiH2 in-phase rocking, which is present for the C2v structure, is forbidden for D2h and hence disappears.
Related Papers
- → Ab initio resonant Raman spectra of diamond-like carbons(2005)56 cited
- → Vibrational Coupling Modulation in n-Alkanethiolate Protected Au25(SR)180 Clusters(2016)24 cited
- → Full-Dimensional Quantum Calculations of Vibrational Levels of NH4+ and Isotopomers on An Accurate Ab Initio Potential Energy Surface(2016)7 cited
- → Ab initio potential energy surface and bound states for the Kr–OCS complex(2011)18 cited
- Ab Initio Calculations of the Potential Energy Curves and Vibrational Levels of SO(1999)