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- W2081098283 abstract "The equilibrium geometries and transition states for interconversion of the CSiH2 isomers in the singlet electronic ground state are optimized at the MP2 and CCSD(T) levels of theory using a TZ2P basis set. The heats of formation, vibrational frequencies, infrared intensities, and rotational constants are also predicted. There are three energy minima on the CSiH2 potential energy surface. Energy calculations at CCSD(T)/TZ2P(fd) + ZPE predict that the global energy minimum is silavinylidene (1), which is 34.1 kcal mol−1 lower in energy than trans-bent silaacetylene (2) and 84.1 kcal mol−1 more stable than the vinylidene isomer (3). The barrier for rearrangement 2→1 is calculated at the same level of theory to be 5.1 kcal mol−1, while for the rearrangement 3→2 a barrier of 2.7 kcal mol−1 is predicted. The natural bond orbital (NBO) population scheme indicates a clear polarization of the C(SINGLE BOND)Si bonds toward the carbon end. A significant ionic contribution to the C(SINGLE BOND)Si bonds of 1 and 2 is suggested by the NBO analysis. The C(SINGLE BOND)Si bond length of trans-bent silaacetylene (2) is longer than previously calculated [1.665 Å at CCSD(T)/TZ2P)]. The calculated carbon-silicon bond length of 2 is in the middle between the C(SINGLE BOND)Si double bond length of 1 (1.721 Å) and the C(SINGLE BOND)Si triple bond of the linear form HCSiH (4), which is 1.604 Å. Structure 4 is a higher-order saddle point on the potential energy surface. © 1996 by John Wiley & Sons, Inc." @default.
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- W2081098283 date "1996-05-01" @default.
- W2081098283 modified "2023-10-12" @default.
- W2081098283 title "Silaacetylene: A possible target for experimental studies" @default.
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- W2081098283 doi "https://doi.org/10.1002/(sici)1096-987x(199605)17:7<781::aid-jcc3>3.0.co;2-o" @default.
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