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Deoxygenation reactions of nitrous oxide assisted by oriented external electric field
Due largely to the high stability and the potential ozone‐depleting, the transformation of greenhouse gas nitrous oxide has gained much attentions. In present paper, a new insight into the deoxygenation of nitrous oxide with silane was reported by using oriented external electric field (OEEF) as a c...
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Published in: | International journal of quantum chemistry 2024-05, Vol.124 (9), p.n/a |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | Due largely to the high stability and the potential ozone‐depleting, the transformation of greenhouse gas nitrous oxide has gained much attentions. In present paper, a new insight into the deoxygenation of nitrous oxide with silane was reported by using oriented external electric field (OEEF) as a catalytic strategy. When the OEEF was employed, the reaction barrier of deoxygenation was marvelously decreased as it was oriented along the positive NO/OSi bond‐axis. Especially the field strength is 300 × 10−4 a.u., the differences are up to 22.4/18.3 kcal mol−1 as compared with that of nonfield. In addition, once the H atom in SiH4 was replaced by methyl, two reaction modes were obtained, in which the deoxygenation process was easier when the N2O captured the H atom attached to the Si atom, not attached to the C atom. Further, the solvent effects of deoxygenation reaction were also considered, but with a weak influence were obtained.
The deoxygenation reactions of greenhouse gas N2O were studied through a novel strategy—oriented external electric field (OEEF) based on DFT calculations. The results demonstrated that OEEF catalyzed this reaction obviously when it was oriented along the positive NO/OSi bond‐axis with the field strength added to 300 × 10−4 a.u. |
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ISSN: | 0020-7608 1097-461X |
DOI: | 10.1002/qua.27384 |