Abstract
The preparation of new pentacoordinate silicon complexes 4–6 from polychloro- or fluoro-silanes and 0–silylated-NJ-dimethylhydrazides is described, along with a typical trigonal-bipyramidal (TBP) crystal structure. Evidence is presented that 4–6 undergo rapid N→Si dissociation-recombination. Coupling constants are reported extending across the dative bond, even at temperatures in which N-Si dissociation is rapid. A Karplus-type correlation between dihedral angles and vicinal coupling constants is shown.
| Original language | English |
|---|---|
| Title of host publication | Organosilicon Chemistry |
| Subtitle of host publication | From Molecules to Materials |
| Publisher | wiley |
| Pages | 494-499 |
| Number of pages | 6 |
| ISBN (Electronic) | 9783527620777 |
| ISBN (Print) | 9783527323470 |
| DOIs | |
| State | Published - 1 Jan 2008 |
Keywords
- multinuclear nmr
- pentacoordinate silicon
- stereodynamics
ASJC Scopus subject areas
- General Chemistry