4.7 Article

Novel N-heterocyclic ylideneamine gold(I) complexes: synthesis, characterisation and screening for antitumour and antimalarial activity

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DALTON TRANSACTIONS
卷 40, 期 7, 页码 1471-1483

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c0dt01312a

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  1. NRF (National Research Foundation of South Africa)
  2. CANSA (the Cancer Association of South Africa)
  3. Alexander Von Humboldt Foundation

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Ylideneamine functionalised heterocyclic ligands, 1,3-dimethyl-1,3-dihydro-benzimidazol-2-ylideneamine (I), 3-methyl-3H-benzothiazol-2-ylideneamine (II) or 3,4-dimethyl-3H-thiazol-2-ylideneamine (III), were employed in the preparation of a series of both charged and neutral gold(I) complexes consisting either of a Au(C6F5) fragment (1-3), a [Au(PPh3)](+) unit (4-6) or a [Au(NHC)](+) unit (7) coordinated to the imine nitrogen of the neutral ylideneamine ligand. These complexes were fully characterised by various techniques including X-ray diffraction. In addition, the antitumour and antimalarial potential of selected compounds were assessed in a preliminary study aimed at determining the medicinal value of such compounds. Complexation of the azol-2-ylideneamine ligands with [Au(PPh3)](+) increases their antitumour as well as antimalarial activity.

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