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首页> 外文期刊>Dyes and Pigments >New fluoroionophores for metal cations based on benzo[d]oxazol-5-yl-alanine bearing pyrrole and imidazole
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New fluoroionophores for metal cations based on benzo[d]oxazol-5-yl-alanine bearing pyrrole and imidazole

机译:基于苯并的金属阳离子的新型氟化铝酸盐[D]恶唑-5-基 - 丙氨酸含吡咯和咪唑

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摘要

Highly emissive heterocyclic alanines bearing a benzo[d]oxazolyl unit functionalised with pyrrole and imidazole at the side chain were synthesised and evaluated as fluorimetric chemosensors for different anions and metal cations. The results obtained by UV-Vis and fluorescence titrations as well as H-1 NMR titrations indicate that there is a strong interaction through the donor N and O atoms at the side chain of the benzoxazolyl-alanines, with high selectivity towards Cu2+ and Pd2+ in a ligand-to-metal complex with 1:2 stoichiometry, and association constants were calculated for some ions. The photophysical and ion sensing properties of these unnatural amino acids suggest that they can be used to obtain bioinspired frameworks for metal ion recognition such as peptides/proteins with chemosensory/probing ability.
机译:含有在侧链上用吡咯和咪唑官能化的苯并[D]恶唑基单元的高发光杂环丙氨酸被合成并评估为不同阴离子和金属阳离子的荧光化学传感器。 通过UV-VIS和荧光滴定以及H-1 NMR滴定获得的结果表明,通过苯并恶唑基 - 丙氨酸侧链的供体N和O原子存在强烈的相互作用,具有高选择性朝向Cu2 +和PD2 + 为一些离子计算配体 - 金属络合物,与1:2的化学计量和合作常数计算。 这些非天然氨基酸的光物理和离子感测性能表明它们可用于获得用于金属离子识别的BioInspired框架,例如具有化学感性/探测能力的肽/蛋白质。

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