Abstract
Reaction of the bidentate Lewis acid 1,2-Fc(SnMe2Cl)(B(Me)Cl) (1, Fc = 1,2-ferrocenylene) with 2-trimethylstannylpyridine gave a complex (2), in which the 2-pyridyl group forms a bridge between the Lewis acidic tin and boron centers. The structure of 2 was confirmed by multinuclear and two-dimensional NMR, single crystal X-ray diffraction, and elemental analysis. The crystal structure shows that the pyridyl moiety is positioned endo relative to the substituted Cp ring and UV-Vis spectroscopy revealed an enhancement of the ferrocene-centered dd transition in comparison to related complexes with pyridine as a terminal ligand.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 162-166 |
| Number of pages | 5 |
| Journal | Inorganica Chimica Acta |
| Volume | 364 |
| Issue number | 1 |
| DOIs | |
| State | Published - Dec 15 2010 |
All Science Journal Classification (ASJC) codes
- Physical and Theoretical Chemistry
- Inorganic Chemistry
- Materials Chemistry
Keywords
- Bidentate Lewis acids
- Boron
- Ferrocene
- Heterocycles
- Reverse chelate
- Tin
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