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The coordination chemistry of fluorescent pyridinyl- and quinolinyl-phthalimide ligands with the {Au-I-PPh3} cationic unit

Research output: Contribution to journalJournal article


  • Lucy A. Mullice
  • Flora L. Thorp-Greenwood
  • Rebecca H. Laye
  • Michael Coogan
  • BM Kariuki
  • Simon J. A. Pope
<mark>Journal publication date</mark>2009
<mark>Journal</mark>Dalton Transactions
Issue number34
Number of pages6
Pages (from-to)6836-6842
<mark>Original language</mark>English


The new mono-dentate ligands, 2-(2-aminoethyl)-N-phthalimido-pyridine (L4) and 8-amino-N-phthalimido-quinoline (L6), were synthesised using a solvent-free melt method. These ligands together with L1–3,5 (3-amino-N-phthalimido-pyridine; 3-aminomethyl-N-phthalimido-pyridine; 4-aminomethyl-N-phthalimido-pyridine; 3-amino-N-phthalimido-quinoline) were then used to access six luminescent AuI complexes of the generic type {Ph3P–Au–Ln}(OTf). X-Ray crystallography has been used to structurally characterise three of the complexes showing that in the cases of L1 and L3 the complexes adopt an approximately linear P–Au–N coordination geometry. However, in the case of the sterically demanding L6 the structure shows distortions within the ligand and deviations from a linear coordination geometry. Solution state 1H and 31P{1H} NMR confirmed that the proposed formulations and coordination modes exist in solution. At room temperature the photophysical studies showed that the emission from each of the six complexes was in the visible region (395–475 nm) and assigned to a ligand-centred fluorescence (τ < 10 ns) in each case.