Abstract
Contrary to the reports on the coordination oi copper (I) to N/P-ambidentate cyclotriphosphazenes, gold (I), gold (III) and dimethylgoldf 111) chloride are found to become exclusively P-coordinated to the prototype ligand 2-methyl-4, 4, 6, 6-tetraphenylcyclotriphosphazene (1). The P-H proton is transferred to an adjacent nitrogen atom of the heterocycle. According to temperature dependent NMR spectra, the AuCl and the AuCl3 complexes are fluxional molecules or ions, resp., with a rapid proton transfer between P-NH-P and P = N-P functions. The behaviour is similar to that of related palladium and platinum complexes, reported previously.
| Original language | English |
|---|---|
| Pages (from-to) | 1286-1288 |
| Number of pages | 3 |
| Journal | Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences |
| Volume | 35 |
| Issue number | 10 |
| DOIs | |
| State | Published - 1 Oct 1980 |
Keywords
- Cyclotriphosphazenes
- Gold Complexes
- N/P-Ambidentate System
- Tautomerism