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Molecularly Imprinted Polymers Based on lodinated Monomers for Selective Room-Temperature Phosphorescence Optosensing of Fluoranthene in Water

机译:含氟单体的分子印迹聚合物用于水中荧蒽的选择性室温磷光光敏化

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摘要

Aiming at enhancing the advantages of traditional mo-lecularly imprinted polymers (MIPs) for chemical sensing,a new MIP design approach introducing an internal heavy atom in their polymeric structure is described.Based on the heavy-atom effect,the novel polymer allows one to perform room-temperature phosphorescence (RTP) trans-duction of the analyte.The synergic combination of a tailor-made MIP recognition with a selective RTP detection is a novel concept for optosensing devices which is assessed here for simple and highly selective determination of trace amounts of fluoranthene in water.The noncovalent MIP was synthesized using the laboratory-synthesized tetraiodobisphenol A as one of the polymeric precursors and fluoranthene as template.In the presence of an oxygen scavenger,the iodide included in the polymeric structure induced efficient RTP emission from the analyte,once recognized by the MIP.The developed optosensing system has demonstrated a high specificity for fluoranthene against other polycyclic aromatic hydrocarbons.Detection limit for the target molecule was 35 ng/L (5-mL sample injections),and the linear range extended above 100 mug/L of the analyte.The polymer can be easily regenerated for subsequent sample injections (at least up to 450 cycles) with acetonitrile.The synthesized sensing material showed good stability for at least 6 months after preparation.The feasibility of monitoring fluoranthene in real samples was successfully evaluated through the analysis of five spiked river water samples.
机译:为了增强传统分子印迹聚合物(MIP)在化学传感中的优势,描述了一种在其聚合物结构中引入内部重原子的MIP设计新方法。基于重原子效应,该新型聚合物可以量身定制的MIP识别与选择性RTP检测的协同结合是光敏器件的一种新颖概念,在此进行了评估,可对痕量进行简单而高度选择性的测定在实验室中合成的四碘双酚A为聚合物前体之一,以荧蒽为模板合成了非共价MIP。 ,一旦获得MIP的认可,开发的光敏系统已显示出对荧蒽荧光素的高度特异性在其他多环芳烃中,目标分子的检测限为35 ng / L(5 mL样品进样),线性范围扩展到100杯/ L以上的分析物。聚合物可以轻松再生用于后续样品进样(合成的传感材料在制备后至少6个月内表现出良好的稳定性。通过分析五个加标的河水样品成功地评估了在实际样品中监测荧蒽的可行性。

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