化学
罗丹明
罗丹明B
胶体金
纳米颗粒
光化学
表面等离子共振
等离子纳米粒子
猝灭(荧光)
共振(粒子物理)
等离子体子
分析化学(期刊)
纳米技术
荧光
有机化学
光电子学
材料科学
光催化
光学
催化作用
物理
粒子物理学
作者
Ming Gao,Hong Yan Zou,Yuan Fang Li,Cheng Zhi Huang
标识
DOI:10.1021/acs.analchem.6b04124
摘要
Plasmonic resonance energy transfer (PRET), which occurs between the plasmonic nanoparticles and organic dyes, has significant potential in target sensing chemistry owing to its sensitivity at the single nanoparticle level. In this contribution, by using AuNPs, which has localized surface plasmonic resonance light scattering (LSPR-LS) around 550 nm, as the donor of PRET, a general sensitive detecting strategy of ions were developed. Targets can specifically react with a ring-close structured rhodamine spirolactam, which was prepared from rhodamines in the presence of different primary amine wherein the option of the primary amine is up to the targets, forming ring-open structured rhodamine spirolactam with the strong absorption around 550 nm. This process triggered the PRET from gold nanoparticles (AuNPs) to the ring-open structured rhodamine spirolactam. As a proof of concept, Cu2+ and Hg2+ were detected by using rhodamine B hydrazide and N-(rhodamine B)lactam-ethylenediamine, respectively. With the aid of a dark field microscope, the LSPR-LS of AuNPs gets decreased within 10 min with the addition of Cu2+ or Hg2+. The scattering light spectra get red-shifted during the targets addition due to the quenching dip phenomenon. Further theoretical simulation indicated the PRET process could be aroused by the electric field diminishment of AuNPs via the interaction of rhodamine. This single nanoparticle based detecting strategy could be further applied for other anions, cations, or small organic molecules detection by simply changing the rhodamine spirolactam.
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