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Pyridyl Azo-Based Progelator in Selective Sensing of Hg2+ and Ag+ Ions via Sol to Gel Conversion

机译:基于吡啶基偶氮的前卫球在Hg2+和Ag+离子的选择性传感中通过溶胶转化为凝胶转化

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摘要

A pyridyl azo-based progelator 1 has been designed and synthesized for selective detection of Hg2+ and Ag+ ions in sol- gel media. Compound 1 acts as nongelator in DMSO-H2O (1:1, v/v) while its aldehyde-counterpart 3 forms stable gel under identical conditions. The specific Hg2+-induced deprotection of the thioacetal functionality in 1 results in in-situ formation of the precursor aldehyde 3 and thereby induces sol-to-gel transformation in DMSO-H2O (1:1, v/v). Gelation is also observed in the presence of Ag+ ion. Interestingly, the gelation modes of 1 in the presence of Hg2+ and Ag+ ions are different. The Hg2+-induced gelation involves dosimetric sensing while the Ag+-induced gelation involves simple metal-ligand non- covalent interaction, as established by using different chelating agents and spectroscopic techniques. The design of metal- responsive low molecular weight gelators (LMWGs) involving protection/deprotection of functional groups in gelator struc- ture is rarely investigated in the literature and hence draws attention.
机译:已经设计并合成了基于吡啶基偶氮的前进剂1,以选择性检测溶液培养基中的Hg2+和Ag+离子。化合物1在DMSO-H2O(1:1,v/v)中充当非元素,而其醛 - 相机3在相同条件下形成稳定的凝胶。特异性的HG2+诱导的硫乙乙化功能的脱旋触摸导致前体醛3的原位形成,从而在DMSO-H2O中诱导Sol-to-Gel转化(1:1,V/V)。在存在Ag+离子的情况下,还观察到凝胶化。有趣的是,在HG2+和Ag+离子存在下1的凝胶化模式不同。 HG2+诱导的凝胶化涉及剂量测定感应,而Ag+诱导的凝胶化涉及简单的金属凸态非共价相互作用,这是通过使用不同的螯合剂和光谱技术来确定的。在文献中很少研究金属响应性低分子量胶凝剂(LMWG),这些胶结中涉及保护/脱落官能团的官能团的官能团的设计,因此很少研究引起人们的注意。

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