Abstract
The introduction of 2-(2-pyridyl)ethyl group on silicon decreases the oxidation potentials of silyl-substituted heteroatom compounds. The molecular orbital calculations indicate that this effect is attributed to the dynamic coordination of the pyridyl group to silicon in the cation radical intermediate. Such coordination also facilitates the selective C-Si bond cleavage.
Original language | English |
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Pages (from-to) | 251-252 |
Number of pages | 2 |
Journal | Chemistry Letters |
Issue number | 3 |
DOIs | |
Publication status | Published - Jan 1 1999 |
Externally published | Yes |
ASJC Scopus subject areas
- Chemistry(all)