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作 者:王红梅[1,2] 赵川德[2] 刘小乐[1,2] 王晓川[1,2]
机构地区:[1]西南科技大学材料科学与工程学院 [2]中国工程物理研究院化工材料研究所,绵阳621010
出 处:《化学通报》2014年第6期572-572,共1页Chemistry
摘 要:本文合成了4-甲基哌嗪-1,8-萘酰亚胺修饰的β-环糊精,该化合物对Fe3+和Fe2+展现出良好的选择性识别能力。当适量的氨水加入到该化合物水溶液中后,溶液体系的荧光被完全猝灭。然而,当Fe3+和Fe2+加入到该溶液体系后,520nm处的荧光信号和416nm处的共振瑞利散射峰均逐渐增强。Fe3+和Fe2+引起的荧光强度和共振瑞利散射强度比值的差异可用于鉴别Fe3+和Fe2+,同时,该方法还展现了较高的灵敏度。本文建立的方法对Fe3+检测的线性范围为1.5×10-5~2.2×10-5mol/L,检测限为1.1×10-5mol/L;对Fe2+检测的线性范围为0.5×10-5~4.2×10-5mol/L,检测限为0.6×10-5mol/L。The fluorescent β-cyclodextrin bearing 4-(methylpiperazinyl) -1,8-naphthalimide ( compound 1) has been synthesized and characterized. The maximum excitation and emission emerged at 411 nm and 520 nm, respectively. After the addition of 8 × 10-4 mol/L ammonia into compound 1 aqueous solution, the fluorescence emission was quenched completely. However, upon adding Fe3+ and Fe2+ , the fluorescence signal of compound 1 enhanced gradually. Meanwhile, a resonance Rayleigh scattering peak at 416 nm increased. The difference of the fluorescence enhancement and the resonance Rayleigh scattering signal can distinguish Fes+ and Fe2+ with pronounced sensitivity and selectivity. The method exhibited a linear response for Fe3+ within the concentration range of 1.5 ×10^-5 -2.2 ×10^-5 mol/L, and the limit of detection was 1. 1 × 10^-5 mol/L. For Fe2+ , the linear range was 0.5× 10^5 -4.2 × 10^-5mol/L, the corresponding limit of detection was 0. 35 × 10^-5 mol/L.
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