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双(偶氮苯酚)杯[4]芳烃与 Ni2+、Co2+、Cu2+、Pb2+和 Hg2+配合物的光学光谱研究。

Optical spectroscopy studies of the complexation of bis(azophenol)calix[4]arene possessing chromogenic donors with Ni2+, Co2+, Cu2+, Pb2+ and Hg2+.

机构信息

Research Laboratory of Synthesis of Inorganic Compounds, Department of Inorganic Chemistry, Faculty of Chemistry, University of Tabriz, Tabriz, Iran.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2012 Dec;98:81-5. doi: 10.1016/j.saa.2012.07.097. Epub 2012 Aug 8.

Abstract

Due to their potential applicability as selective receptors in electrochemical or optical sensors, a bis(azophenol)calix[4]arene derivative H(2)L has been investigated. The complexation properties of this molecule towards Ni(2+) and Co(2+) metal ions has been studied. It is revealed that this ligand exhibits tetradentate with N(2)O(2) core when bound to Ni (II) or Co (II) metal ion. The optical response of azo groups of H(2)L towards Ni(2+), Co(2+), Cu(2+), Pb(2+) and Hg(2+) metal ions has been investigated in DMSO by UV-vis spectroscopy. The absorption spectra of calix[4]arene with cations show marked changes, especially for Co(2+) ion. Furthermore, Job's plot indicate 1:1 binding-stiochiometry for calix[4]arene with Co(2+) ion and Benson-Hilderbrand plot is used for the determination of its association constant. The investigation of UV-vis spectra of chromogenic calix[4]arene in different solvents shows that cis-trans isomerization of azo groups probably depends on kind of solvent. Also the different between the polarity and viscosity of organic solvents used is likely responsible for the changes of the band shape of the spectra.

摘要

由于其作为电化学或光学传感器中选择性受体的潜在适用性,研究了一种双(偶氮苯酚)杯[4]芳烃衍生物 H(2)L。该分子对 Ni(2+)和 Co(2+)金属离子的络合性质进行了研究。结果表明,该配体与 Ni(II)或 Co(II)金属离子结合时表现出四齿配位的 N(2)O(2)核。通过紫外可见光谱法研究了 H(2)L 的偶氮基团对 DMSO 中 Ni(2+)、Co(2+)、Cu(2+)、Pb(2+)和 Hg(2+)金属离子的光学响应。与阳离子结合的杯[4]芳烃的吸收光谱显示出明显的变化,特别是对于 Co(2+)离子。此外,Job 图表明杯[4]芳烃与 Co(2+)离子的结合比为 1:1,Benson-Hilderbrand 图用于测定其缔合常数。不同溶剂中显色杯[4]芳烃的紫外可见光谱研究表明,偶氮基团的顺反异构化可能取决于溶剂的种类。此外,所用有机溶剂的极性和粘度的差异可能是导致光谱带形状变化的原因。

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