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Single sensors for multiple analytes employing fluorometric differentiation for Cr3+ and Al3+ in semi-aqueous medium with bio-activity and theoretical aspects

机译:具有荧光活性的半水介质中的Cr3 +和Al3 +荧光分光光度法用于多种分析物的单一传感器

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The structurally characterized (through single crystal X-ray diffraction) Schiff base ligand N,N′-bis(4-methoxy-salicylaldehyde)azine (H2SALNN) exhibits poor fluorescence in the excited state, due to rotational (cis/trans) isomerization along the azomethine group. However, in the presence of Cr3+ and Al3+ the isomerization is blocked due to coordination with the metal ions exhibiting turn-on fluorescence. The fluorescence enhancement for Al3+ and Cr3+ at two distinct wavelengths shows much difference of the wavelengths (ΔI = 63 nm). Thus, the selective turn-on fluorescence behaviour of H2SALNN for Cr3+ and Al3+ is based on the blocking effect of CN isomerization and chelation-enhanced fluorescence (CHEF). The coordination modes of the complexes were investigated by spectroscopic and computational studies.
机译:结构特征(通过单晶X射线衍射)的席夫碱配体N,N'-双(4-甲氧基-水杨醛)嗪(H2SALNN)在激发态下表现出较弱的荧光,这是由于沿顺式(顺式/反式)异构化甲亚胺基。但是,在Cr3 +和Al3 +的存在下,由于与显示开启荧光的金属离子的配位作用,异构化被阻止了。 Al3 +和Cr3 +在两个不同的波长处的荧光增强显示出波长的很大差异(ΔI= 63 nm)。因此,H2SALNN对Cr3 +和Al3 +的选择性开启荧光行为是基于CN异构化和螯合增强荧光(CHEF)的阻断作用。通过光谱学和计算研究研究了配合物的配位方式。

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