Theoretical study on structures and stability of SiC₃S isomers

Abstract

Various levels of calculations are carried out to explore the potential energy surfaces (PES) of singlet and triplet SiC₃S, a molecule of potential interest in interstellar chemistry. At the DFT/B3LYP/6-311G(d) level, a total of 57 minimum isomers and 92 interconversion transition states are located. The structures of the most relevant isomers and transition states are further optimized at the QCISD/6-311G(d) level followed by CCSD(T)/6-311 + G(2df) single-point energy calculations. At the QCISD level, the lowest-lying isomer is the chain-like SiCCCS ³ 1 (0.0 kcal/mol) with a great kinetic stability of 54.1 kcal/mol. In addition, ring isomers CC-cCSSi ¹ 9 (19.8 kcal/mol), S-cCCCSi ¹ 12 (30.4 kcal/mol), S-cCCSiC ¹ 18 (9.4 kcal/mol), S-cSiCCC ¹ 21 (34.4 kcal/mol) and cage-like isomer cage-SiSCCC ¹ 23 (51.8 kcal/mol) also possess considerable kinetic stability (more than 10.0 kcal/mol). As a result, these six isomers are predicted to be possible candidates for future experimental and astrophysical detection. The bond natures and possible formation pathways in interstellar space of the SiCCCS are discussed. The predicted structure and spectroscopic properties for it are expected to be informative for the identification of SiC₃S and even larger SiC _n S species either in laboratory or in space.

Keywords:

• Theoretical study
• Structure
• Stability
• Potential energy surface (PES)
• SiC₃S

Acknowledgements

This work is supported by the National Nature Science Foundation of China (No. 20333050, 20643004), Excellent Young Foundation of Jilin Province, and Technology Development Project of Jilin Province (20050906-6).