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- W2985233126 abstract "Thermal decomposition of hexamethyldisilane (HMDS) was studied from room temperature to 1310 K using flash pyrolysis vacuum ultraviolet single-photon ionization time-of-flight mass spectrometry (VUV-SPI-TOFMS). Decomposition pathways of HMDS and initial reaction intermediates were also investigated using density functional theory (DFT) at the B3LYP/6-311++G(d,p) level. Unimolecular decomposition reactions of HMDS involving Si-Si and Si-C bond cleavage, as well as decomposition producing Me4Si and :SiMe2 via a three-centered elimination, were determined as the initiation reactions. Me3SiSi(Me)2•, Me4Si, Me3Si•, and :SiMe2 were major products of the initiation reactions. These initial products were apt to decompose by homolytic reactions. Me2Si═CH2, :SiMe2, and other silene/silylene intermediates preferred decomposing through molecular eliminations. Both homolytic and molecular elimination reactions are important in the pyrolysis of HMDS." @default.
- W2985233126 created "2019-11-22" @default.
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- W2985233126 date "2019-11-11" @default.
- W2985233126 modified "2023-09-23" @default.
- W2985233126 title "Mechanistic Study of Thermal Decomposition of Hexamethyldisilane by Flash Pyrolysis Vacuum Ultraviolet Photoionization Time-of-Flight Mass Spectrometry and Density Functional Theory" @default.
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- W2985233126 doi "https://doi.org/10.1021/acs.jpca.9b08102" @default.
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