Abstract
The synthesis and photophysical characterisation are reported of a series of cationic, neutral and anionic europium and terbium complexes based on structurally related, nonadentate ligands based on the cyclen macrocycle. Each complex incorporates a tetraazatriphenylene moiety and overall absolute emission quantum yields are in the range 15-40% in aerated aqueous media. Dynamic quenching of the lanthanide excited state occurs with electron-rich donors, e.g. iodide, ascorbate and urate, and a mechanistic interpretation is put forward involving an electron transfer process. The cationic lanthanide complexes are taken up by N1H/3T3 cells and tend to localise inside the cell nucleus.
| Original language | English |
|---|---|
| Pages (from-to) | 1013-1024 |
| Number of pages | 12 |
| Journal | Organic and Biomolecular Chemistry |
| Volume | 3 |
| Issue number | 6 |
| DOIs | |
| Publication status | Published - 2 Mar 2005 |
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SDG 9 Industry, Innovation, and Infrastructure
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