Abstract
The [(SePPh(2))(2)N](-) ligand 1c forms stable tris(chelates) with the Sb-III, Bi-III, and In-III ions. The crystal and molecular structures of the resulting compounds 3, 4, and 5 were determined by X-ray diffractometry. The coordination geometry around the metal centers can be described as a distorted octahedron. This feature and the results obtained by comparing the structures with their sulfur and oxygen analogs lead us to conclude that in both Sb-III and Bi-III compounds the arrangement around the metals suggests a stereochemically nonactive electron lone pair.
| Original language | English |
|---|---|
| Pages (from-to) | 919-923 |
| Number of pages | 5 |
| Journal | Chemische Berichte |
| Volume | 129 |
| Issue number | 8 |
| DOIs | |
| Publication status | Published - Aug 1996 |
Keywords
- phosphazene metallacycles
- [N-(diphenylphosphinoselenoyl)-P,P-diphenylphosphinoselenoic amidato-Se,Se'] chelates
- inorganic carbon-free chelate rings
- octahedral MSe(6) core (M=Sb, Bi, and In)
- POLYFUNCTIONAL MOLECULES
- CRYSTAL
- SULFUR
- ENLARGEMENT
- REACTIVITY
- CHEMISTRY
- SELENIUM
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