Abstract
Two new, potentially cyclometalating terdentate ligands bearing phosphonate substituents, Et2O3PN^
C(H)^N (5) and Et2O3P-C(H)^N^N (7), have been prepared. The corresponding ruthenium complexes,
[1]+ and [2]+, respectively, were obtained by reaction with [RuCl3(tpy)]. Complexes [1]+ and [2]+ display
electronic properties characteristic for cyclometalated ruthenium complexes. The platinum complex [3],
of N^C(H)^N ligand 5, was also prepared and is highly phosphorescent in solution. In general, the phosphonate
group electronically behaves equivalent to a carboxylate moiety.
| Original language | English |
|---|---|
| Pages (from-to) | 1701-1706 |
| Number of pages | 6 |
| Journal | Inorganica Chimica Acta |
| Volume | 363 |
| Issue number | 8 |
| DOIs | |
| Publication status | Published - 2010 |
Keywords
- Cyclometalated
- Ruthenium
- Spectroscopy
- Phosphonate
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