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功能化多胺配体的荧光锌(II)配合物用于阴离子检测。

Anion detection by fluorescent Zn(II) complexes of functionalized polyamine ligands.

作者信息

Rodríguez Laura, Lima João C, Parola A Jorge, Pina Fernando, Meitz Robert, Aucejo Ricardo, Garcia-España Enrique, Llinares José M, Soriano Conxa, Alarcón Javier

机构信息

Departamento de Quimica, REQUIMTE, Faculdade de Ciencias e Tecnologia, Universidade Nova de Lisboa, Portugal.

出版信息

Inorg Chem. 2008 Jul 21;47(14):6173-83. doi: 10.1021/ic7023956. Epub 2008 Jun 26.

Abstract

The Zn(2+) coordination chemistry and luminescent behavior of two ligands constituted by an open 1,4,7-triazaheptane chain functionalized at both ends with 2-picolyl units and either a methylnaphthyl (L1) or a dansyl (L2) fluorescent unit attached to the central amino nitrogen are reported. The fluorescent properties of the ZnL1(2+) and ZnL2(2+) complexes are then exploited toward detection of anions. L1 in the pH range of study has four protonation constants. The fluorescence emission from the naphthalene fluorophore is quenched either at low or at high pH values leading to an emissive pH window centered around pH = 5. In contrast, in L2 the fluorescence emission from the dansyl unit occurs only at basic pH values. In the case of L1, a red-shifted band appearing in the visible region was assigned to an exciplex emission involving the naphthalene and the tertiary amine of the polyamine chain. L1 forms Zn(2+) mononuclear complexes of ZnH(p)L1((p+2)+) stoichiometry with p = 1, 0, -1. Formation of the ZnL1(2+)species produces a strong enhancement of the L1 luminescence leading to an extended emissive pH window from pH = 5 to pH = 9. Addition of several anions to this last complex leads to a partial quenching effect. On the contrary, the fluorescence emission of L2 is partially quenched upon complexation with Zn(2+) in the same pH window (5 < pH < 9). The lower stability of ZnL2(2+) with respect to ZnL1(2+) suggests a lack of involvement of the sulfonamide group in the first coordination sphere. However, there is spectral evidence for an interesting photoinduced binding of the sulfonamide nitrogen to Zn(2+). While addition of diphosphate, triphosphate, citrate, and D,L-isocitrate to a solution of ZnL2(2+) restores the fluorescence emission of the system (lambda max ca. 600 nm), addition of phosphate, chloride, iodide, and cyanurate do not produce any significant change in fluorescence. Moreover, this system would permit one to differentiate diphosphate and triphosphate over citrate and d, l-isocitrate because the fluorescence enhancement observed upon addition of the first anions is much sharper. The ZnL2(2+) complex and its mixed complexes with diphosphate, triphosphate, citrate, and D,L-isocitrate have been characterized by (1)H, (31)P NMR, and Electrospray Mass Spectrometry.

摘要

报道了由一个开放的1,4,7 - 三氮杂庚烷链构成的两种配体的锌(II)配位化学和发光行为,该链两端用2 - 吡啶甲基单元官能化,并且在中心氨基氮上连接有一个甲基萘基(L1)或一个丹磺酰基(L2)荧光单元。然后研究了ZnL1(2+)和ZnL2(2+)配合物的荧光性质用于阴离子检测。在研究的pH范围内,L1有四个质子化常数。萘荧光团的荧光发射在低pH值或高pH值时被猝灭,导致以pH = 5为中心的发光pH窗口。相反,在L2中,丹磺酰单元的荧光发射仅在碱性pH值下出现。对于L1,在可见光区域出现的一个红移带被归因于涉及萘和多胺链叔胺的激基复合物发射。L1形成化学计量比为ZnH(p)L1((p + 2)+)(p = 1, 0, -1)的锌(II)单核配合物。ZnL1(2+)物种的形成导致L1发光强烈增强,从而使发光pH窗口从pH = 5扩展到pH = 9。向该最后一种配合物中加入几种阴离子会导致部分猝灭效应。相反,在相同的pH窗口(5 < pH < 9)中,L2与锌(II)络合时荧光发射会部分猝灭。ZnL2(2+)相对于ZnL1(2+)稳定性较低,这表明磺酰胺基团未参与第一配位层。然而,有光谱证据表明磺酰胺氮与锌(II)存在有趣的光诱导结合。当向ZnL2(2+)溶液中加入二磷酸、三磷酸、柠檬酸和D,L - 异柠檬酸时,体系的荧光发射恢复(最大波长约600 nm),而加入磷酸、氯离子、碘离子和氰尿酸盐时荧光没有显著变化。此外,该体系能够区分二磷酸和三磷酸与柠檬酸和D,L - 异柠檬酸,因为加入前一种阴离子时观察到的荧光增强要尖锐得多。ZnL2(2+)配合物及其与二磷酸、三磷酸、柠檬酸和D,L - 异柠檬酸的混合配合物已通过(1)H、(31)P NMR和电喷雾质谱进行了表征。

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