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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Ratiometric fluorescence off-on-off sensor for Cu ~(2+) in aqueous buffer by a lower rim triazole linked benzimidazole conjugate of calix[4]arene
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Ratiometric fluorescence off-on-off sensor for Cu ~(2+) in aqueous buffer by a lower rim triazole linked benzimidazole conjugate of calix[4]arene

机译:杯状[4]芳烃下缘三唑连接的苯并咪唑共轭物用于水溶液中Cu〜(2+)的比例荧光开-关传感器

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摘要

A benzimidazole appended triazole linked 1,3-diconjugate of calix[4]arene (L) has been synthesized and characterized. The conjugate L has been found to recognize Cu ~(2+) among the thirteen different metal ions studied by exhibiting ratiometric fluorescence changes through newly generated excimer band at ~380 nm. Fluorescence off-on-off behavior has been clearly demonstrated on the basis of the binding variability of Cu ~(2+) to L. The binding has been elicited through the changes observed in the fluorescence, ESI MS and 1H NMR titrations. All the other metal ions studied do not show any new band and further do not interfere with the recognition of Cu ~(2+) by L, even when these are present in the same medium. The structural features of both the mono- and di-nuclear complexes were established by DFT computational calculations and found to display highly distorted geometry about the copper centers that deviate from both the tetrahedral and the square planar.
机译:合成并表征了苯并咪唑附加的三唑连接的杯[4]芳烃(L)的1,3-二共轭物。通过在约380 nm处通过新产生的准分子带表现出比例荧光变化,已发现共轭L可识别13种金属离子中的Cu〜(2+)。根据Cu〜(2+)与L的结合变异性,已经清楚地证明了荧光的开关行为。结合是通过在荧光,ESI MS和1H NMR滴定中观察到的变化引起的。研究的所有其他金属离子均未显示任何新谱带,并且即使它们存在于相同的介质中,也不会干扰L对Cu〜(2+)的识别。单核和双核配合物的结构特征都是通过DFT计算计算建立的,发现它们在偏离四面体和正方形平面的铜中心周围显示出高度扭曲的几何形状。

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