Abstract
Introduction of a chiral ligand to a series of pentacoordinate silicon complexes led to the assignment of two intramolecular rate processes: Si-N cleavage and pseudorotation. Linear correlations between 15N and 29Si chemical shifts of the complexes, as well as between the latter and the N-methyl exchange barriers were attributed to variation in strength of N→Si coordination.
| Original language | English |
|---|---|
| Title of host publication | Organosilicon Chemistry III |
| Subtitle of host publication | From Molecules to Materials |
| Publisher | wiley |
| Pages | 446-451 |
| Number of pages | 6 |
| ISBN (Electronic) | 9783527619900 |
| ISBN (Print) | 9783527620746 |
| DOIs | |
| State | Published - 1 Jan 2008 |
Keywords
- Multinuclear NMR
- Pentacoordinate
- Stereodynamics
ASJC Scopus subject areas
- General Chemistry
- General Engineering
- General Materials Science
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