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Benzylidenecyclohexanone-triazole-based conjugated polymer: Click synthesis, Staudinger end-capping and application as optical probe scaffold

机译:基于亚苄基环己酮-三唑的共轭聚合物:点击合成,施陶丁格封端及其在光学探针支架中的应用

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A type of benzylidenecyclohexanone-triazole based conjugated polymer (P5) was successfully synthesized by Cu+-catalyzed Click reaction. The THE solution of P5 exhibited specific optical response (increase in absorption and decrease in fluorescence) toward I. With the further addition of Hg2+ into the assembly of P5-I-, distinctive recovery of optical properties was detected, suggests that P5-I- adduct can act as fluorescence turn-on probing platform for Hg2+. Post-polymerization of P5 was implemented by catalyst-free Staudinger reaction between P5 and triphenylphosphine to afford phosphinimine-endcapped polymer (P5-TPP). Different from the blue-greenish emission (similar to 490 nm) of P5, P5-TPP emitted yellow light (similar to 550 nm) in THE water mixture (V-THF/V-water = 2/8). P5-TPP displayed specific fluorescence ratiometric alteration toward hypochlorite ion in THE water mixture (V-THF/V-water = 2/8, pH = 7.4), which might be due to the hypochlorite-induced hydrolysis of phosphinimine energy-transfer acceptors in P5-TPP. The results suggest that P5 can act as structure scaffold for the construction of optical probe for triple analytes (I-, Hg2+ and ClO-). (C) 2016 Elsevier Ltd. All rights reserved.
机译:通过Cu +催化的Click反应成功合成了一种亚苄基环己酮-三唑基共轭聚合物(P5)。 P5的THE溶液对I表现出特定的光学响应(吸收增加,荧光减少)。随着H52 +进一步添加到P5-I-的组装物中,检测到独特的光学性能恢复,表明P5-I-加合物可以充当Hg2 +的荧光开启探测平台。 P5的后聚合是通过P5与三苯膦之间的无催化剂Staudinger反应进行的,以提供膦亚胺封端的聚合物(P5-TPP)。与P5的蓝绿色发射光(约490 nm)不同,P5-TPP在THE水混合物(V-THF / V-水= 2/8)中发出黄光(约550 nm)。 P5-TPP在水混合物中对次氯酸根离子表现出特定的荧光比率变化(V-THF / V-水= 2/8,pH = 7.4),这可能是由于次氯酸根诱导的次磷酸亚胺能量转移受体的水解。 P5-TPP。结果表明,P5可以作为构建三重分析物(I-,Hg2 +和ClO-)的光学探针的结构支架。 (C)2016 Elsevier Ltd.保留所有权利。

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