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首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >Calix[4]arene based fluorescent chemosensor bearing coumarin as fluorogenic unit: Synthesis, characterization, ion-binding property and molecular modeling
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Calix[4]arene based fluorescent chemosensor bearing coumarin as fluorogenic unit: Synthesis, characterization, ion-binding property and molecular modeling

机译:以香豆素为荧光单元的基于杯[4]芳烃的荧光化学传感器:合成,表征,离子结合性质和分子建模

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摘要

A series of calix[4]arene-based fluorescent chemosensors in cone and 1,3-alternate conformations have been synthesised incorporating ethylene glycol units as binding sites and coumarin as fluorescent probe. These compounds have been designed with variation in substituents, conformations of the calixarene unit and steric crowding. The open chain ethylene glycol moieties are flexible so that they can orient themselves in space to make effective interactions with metal ions. Ion-binding study of these fluoroionophores has been carried out using a large number of metal ions and the ion recognition event is monitored by fluorescence and absorption spectroscopy. Substantial quenching in emission intensity in presence of Fe~(3+) and Cu~(2+) and enhancement of emission intensity in presence of Ca~(2+) suggests strong binding of these metal ions with the ionophores. Complexation with these metal ions is also evident from UV-Vis spectral changes. Composition of the complexes formed (1:1) has been confirmed by ESMS analysis. Binding constants with the strongly interacting metal ions have been evaluated from fluorescence titration data. DFT calculations have been carried out to find out the metal binding sites of the calix ionophores and frontier molecular orbital analyses have rationalized the fluorescence behaviors observed upon complexation with metal ions in these cases.
机译:已经合成了一系列圆锥形和1,3-交替构型的杯芳烃[4]芳烃基荧光化学传感器,其中结合了乙二醇单元作为结合位点和香豆素作为荧光探针。设计这些化合物时,其取代基,杯芳烃单元的构象和空间拥挤均会发生变化。开链乙二醇部分是柔性的,因此它们可以在空间中定向以与金属离子有效地相互作用。这些氟离子载体的离子结合研究已使用大量金属离子进行,离子识别事件通过荧光和吸收光谱法进行监测。在Fe〜(3+)和Cu〜(2+)存在下,发射强度发生明显的猝灭,而在Ca〜(2+)存在下,发射强度增强,表明这些金属离子与离​​子载体牢固结合。从UV-Vis光谱变化还可以看出与这些金属离子的络合。通过ESMS分析已确认形成的复合物的组成(1:1)。从荧光滴定数据已经评估了与强相互作用金属离子的结合常数。已经进行了DFT计算,以发现杯状离子载体的金属结合位点,并且在这些情况下,前沿分子轨道分析已使与金属离子络合时观察到的荧光行为合理化。

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