Institut für Organische Chemie, Technische Universität Bergakademie Freiberg, Leipziger Str. 29, D-09596 Freiberg/Sachsen, Germany.
Org Biomol Chem. 2009 Dec 7;7(23):4904-17. doi: 10.1039/b911800d. Epub 2009 Oct 8.
A series of new fluorescent calix[4]arenes (2-7; 5 has been isolated as two not yet described conformational isomers) featuring two directly lower rim attached dansyl moieties besides other lower or upper rim site substituents have been synthesized and investigated with reference to their fluorescence properties including potential sensing capability for metal ions. Except for the nitro substituted compound 7, which showed a moderate fluorescence quenching on the addition of Hg2+ in acetonitrile, the calixarenes 2-6 were found to selectively recognize Cu2+ in the 10(-6) mol L(-1) concentration range detectable by the nearly total quenching of their intrinsic fluorescence. Using fluorescence titration experiments, the ideal complexation ratio [metal ion]/[ligand] for three exemplarily investigated calixarenes (3, 5a and 7) was determined to be 2:1. For 5a, a new red shifted signal was observed by the complexation of Cu2+ while the addition of Hg2+ only yields a moderate quenching of the parent signal, indicating a different binding mode for both metal ions. This finding enables the calixarene 5a to be used as a suitable chemosensor for the simultaneous determination of copper and mercury. In this paper we also present the first crystal structures of dansylated calixarenes having the dansyl groups directly attached to the lower rim site. They involve the unsolvated calixarene 5b and the two solvent inclusion compounds 2.CH2(OH)CN and 3.3CH3CN, each showing an extensive pattern of non-covalent interactions. In both solvates, the calixarenes are fixed in a cone conformation while the unsolvated calixarene 5b adopts the partial cone conformation. A solution 1H NMR study in CDCl3 reveals also the cone conformation for all dansylated calixarenes, except the more conformationally flexible upper rim unsubstituted calixarene 5 which showed cone and partial cone conformers 5a and 5b, respectively, in an approximate 2:3 ratio.
一系列新的荧光杯[4]芳烃(2-7;5 已被分离为两种尚未描述的构象异构体)具有两个直接连接在下缘的丹磺酰基部分,以及其他下缘或上缘部位取代基,已经被合成并研究了它们的荧光性质,包括对金属离子的潜在传感能力。除了硝基取代的化合物 7,在乙腈中加入 Hg2+时显示出中等程度的荧光猝灭外,杯[4]芳烃 2-6 被发现能够选择性地识别 Cu2+,在 10(-6)mol L(-1)浓度范围内可检测到,其本征荧光几乎完全猝灭。通过荧光滴定实验,确定了三种典型的杯芳烃(3、5a 和 7)的理想络合比[金属离子]/[配体]为 2:1。对于 5a,当与 Cu2+络合时观察到新的红移信号,而加入 Hg2+仅导致母体信号适度猝灭,表明两种金属离子的结合模式不同。这一发现使杯芳烃 5a 能够作为同时测定铜和汞的合适化学传感器。在本文中,我们还首次报道了将丹磺酰基直接连接到下缘位置的丹磺酰基杯芳烃的晶体结构。它们涉及未溶剂化的杯芳烃 5b 和两种溶剂包合物 2.CH2(OH)CN 和 3.3CH3CN,每个都显示出广泛的非共价相互作用模式。在两种溶剂化物中,杯芳烃都固定在锥型构象中,而未溶剂化的杯芳烃 5b 则采用部分锥型构象。在 CDCl3 中的溶液 1H NMR 研究也表明,除了构象更灵活的上缘未取代杯芳烃 5 外,所有丹磺酰基杯芳烃都采用锥型构象,5 分别以 5a 和 5b 的形式存在,比例约为 2:3。