对映体
胶体
材料科学
吸附
罗丹明
对映体过量
检出限
表面改性
化学工程
化学
纳米技术
组合化学
溶剂
纳米材料
分子
选择性吸附
分子识别
选择性
拉曼光谱
相(物质)
手性(物理)
分析物
分子结合
表面增强拉曼光谱
分子印迹
有机化学
罗丹明B
作者
Xuegang Zhang,Qiang Wang,Huijuan Zhang,Yan Zhao,Yijian Jiang,Yinzhou Yan
标识
DOI:10.1021/acs.jpcc.5c07646
摘要
Porous metal–organic frameworks (MOFs) facilitating molecular enrichment and chemical enhancement hold promise as enhancers for surface-enhanced Raman spectroscopy (SERS). The nanochannels in MOFs provide abundant binding sites for modification with chiral amino acids for enantiomeric discrimination. Here we develop a solvent-regulated method to synthesize plasmon-free Zn-BTC microflower (Zn-BTC MF) with a high surface area of 346 ± 14 m2/g as SERS colloids. The morphology and surface area of Zn-BTC are effectively controlled by an ethanol/DMF solvent combination strategy, significantly promoting the molecular adsorption for detection. Combining with the charge-transfer-resonance chemical enhancement, the Zn-BTC SERS colloids provide an enhancement factor of 1.1 × 104 with the limit of detection down to 10–8 M for rhodamine 6G. The l-lysine@Zn-BTC MF is further synthesized by postmodification via an EDC/NHS coupling reaction for quantitative chiral recognition of d-histidine, a typical biomarker for clinical diagnosis of diseases, with the g-factor up to 1.16 ± 0.06 at the concentrations down to 10–5 M. This present work paves a new way to design and synthesize plasmon-free MOFs-based SERS colloids for trace enantiomeric discrimination.
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