Abstract
The reaction of [Et 4N][Mo(CSe)(CO) 2(Tp*)] (Tp* = hydrotris(3,5-dimethylpyrazol-1-yl)borate) with [Rh 2(μ-Cl) 2(η 4-cod) 2] (cod = cyclo-octa-1,5-diene) results in the formation of the tetrametallic complex [Rh 2{SeCMo(CO) 2(Tp*)} 2(η 4- cod) 2] in which the CSe ligand adopts a crystallographically confirmed and unprecedented μ 3:σ,σ′(Se), σ″(C) coordination mode.
| Original language | English |
|---|---|
| Pages (from-to) | 2482-2485 |
| Number of pages | 4 |
| Journal | Organometallics |
| Volume | 31 |
| Issue number | 6 |
| DOIs | |
| Publication status | Published - 26 Mar 2012 |
Fingerprint
Dive into the research topics of 'Novel carbon monochalcogenide coordination mode: [Rh 2{μ- SeCMo(CO) 2(Tp*)} 2(η 4-cod) 2] (Tp* = hydrotris(3,5-dimethylpyrazol-1-yl)borate; Cod = cyclo-octa-1,5-diene)'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver