Design and synthesis of triazolyl coumarins as Hg super(2+) selective fluorescent chemosensors

• Published in: Analyst (London) Vol. 137; no. 24; pp. 5770 - 5776
• Main Authors: Ho, I-Ting, Lai, Ting-Ling, Wu, Ren-Tsung, Tsai, Ming-Tsung, Wu, Chun-Ming, Lee, Gene-Hsiang, Chung, Wen-Sheng
• Format: Journal Article
• Language: English
• Published: 01.11.2012
• Subjects: Binding; Coumarin; Derivatives; Ethers; Ligands; Nitrogen atoms; Selectivity; Triazoles
• ISSN: 0003-2654; 1364-5528
• DOI: 10.1039/c2an36076d

A series of triazolyl coumarin derivatives L1-L4, with and without spacer groups between the coumarin and the triazole groups, were synthesized as fluorescent sensors to study their binding ability and selectivity toward metal ions. Ligand L3, which contains an acetyl linker between the triazole and the coumarin, exhibited a high selectivity toward Hg super(2+) in polar protic solvents MeOH-CHCl sub(3) (9 : 1, v/v) with fluorescent enhancement, furthermore, it was found to bind two Hg super(2+) at a high concentration (>12.5 mM) of Hg(ClO sub(4)) sub(2). In contrast, L4, in which position 4 of the triazole unit was replaced by a benzyl group instead of the 4-tert-butylphenoxymethyl group used in L1-L3, showed a binding stoichiometry toward only one Hg super(2+). On the basis of the fluorescent sensing, IR, and super(1)H NMR titration results of ligands L1-L4, we proposed that not only the acetyl C&z.dbd; O but also the ether group of the 4-tert-butylphenoxymethyl of L3 assisted the triazole nitrogen atoms in the complexation of Hg super(2+) to form a 1 : 2 complex (L3.(Hg super(2+)) sub(2)).