Structures, relative stability and dissociation of [Si,N,C,O]2+ isomers |
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Authors: | Chi Yujuan Yu Haitao Fu Honggang Li Zesheng SUN Jiazhong |
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Affiliation: | 1. College of Chemistry and Chemical Engineering, Heilongjiang University, 150080, Harbin, China 2. State Key Laboratory of Theoretical and Computational Chemistry Institute of Theoretical Chemistry, Jilin University, 130023, Changchun, China
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Abstract: | Fifteen isomers of [Si,N,C,O]2+ system are obtained at UB3LYP/6-311G(d) and UCCSD(T)/6-311+G(2df) (single-point) levels. The analyses are made for predicting the structures of optimized isomers, while ionic fragments with lower energies are suggested. The calculated results indicate that linear isomer SiNCO2+(2Π) is thermodynamically the most stable species in [Si,N,C,O]2+ system, followed by linear SiOCN2+ (2Π), SiCNO2+ (2Π), and SiC(NO) (2A) with NCO three-membered ring. The order of stability of several kinetically stable isomers is SiNCO2> SiCNO2+ (2Π)>SiOCN2+>SiC(NO)2+>OSiNC2+ (2Π). The obtained results by analyzing the isomerizations and ionic fragment patterns show that the signal peaks of [Si,N,C,O]2+ are attributed to the contribution of linear SiNCO2+ species, which is metastable and can dissociate to the ionic fragments in the mass spectrometry experiments. |
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