Abstract
The reaction of [Et3NH][(μ-RE)(μ-CO)Fe2(CO)6] (E=S, Se) (1) with aryl azides gives bridging triazenido complexes (μ-RE)(μ-p-R1C6H4N3H)Fe 2(CO)6 (2-8) (2, RE=ButS, R1=H; 3, RE=PhS, R1=H; 4, RE=ButS, R1=Cl; 5, RE=ButS, R1=MeO; 6, RE=PhS, R1=MeO; 7, RE=PhSe, R1=H; 8, RE=PhSe, R1=Cl). These complexes were characterized by elemental analyses and 1H-NMR and IR spectroscopy. The structure of complex 2, established by single-crystal X-ray diffraction analysis, shows that the triazenido ligand binds to two iron centers in a bridging bidentate fashion.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 87-92 |
| Number of pages | 6 |
| Journal | Journal of Organometallic Chemistry |
| Volume | 601 |
| Issue number | 1 |
| DOIs | |
| State | Published - Apr 20 2000 |
| Externally published | Yes |
Keywords
- Complex
- Iron
- Selenium
- Structure
- Sulfur
- Triazenido ligand
ASJC Scopus subject areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry
- Inorganic Chemistry
- Materials Chemistry
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