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马来酰胺功能化金纳米粒子用于选择性、比色检测三价镧系离子。

Malonamide-functionalized gold nanoparticles for selective, colorimetric sensing of trivalent lanthanide ions.

机构信息

Department of Chemistry and Materials Science Institute, University of Oregon, Eugene, Oregon 97403-1253, USA.

出版信息

Anal Chem. 2009 Dec 15;81(24):10246-53. doi: 10.1021/ac902271t.

Abstract

A selective and sensitive molecular sensor for trivalent lanthanide (Ln(3+)) ions based upon a malonamide-functionalized gold nanoparticle was developed for colorimetric detection in water. A new synthetic approach permits nanoparticle synthesis, stabilization, and incorporation of a selective lanthanide binding site in a single, direct step. The design incorporates a specifically tailored dual function precursor ligand that bears a sodium thiosulfate (Bunte salt) group that links to the gold nanoparticle core and a tetramethylmalonamide (TMMA) group that serves as a selective Ln(3+) binding site. The sensor's colorimetric response to lanthanide ions is immediate, and it is sensitive down to approximately 50 nM for Eu(3+) and Sm(3+). This study demonstrates a general strategy for direct, convenient nanoparticle synthesis that enables the incorporation of analyte binding groups directly to the nanoparticle surface, allowing colorimetric sensors to be developed for widespread use. The one-step synthesis offers uniform surface ligand composition, reduces the volume of waste generated during nanoparticle synthesis and purification, produces functionalized gold nanoparticles that are stable in nonmodified aqueous environments, and offers colorimetric detection at ambient temperature.

摘要

一种基于丙二酰胺功能化金纳米粒子的用于三价镧系(Ln(3+))离子的选择性和灵敏的分子传感器已被开发用于水相中的比色检测。一种新的合成方法允许在单个直接步骤中进行纳米粒子的合成、稳定和选择性镧系结合位点的掺入。该设计采用了专门设计的双功能前体配体,它带有连到金纳米粒子核心的连二亚硫酸钠(Bunte 盐)基团和作为选择性 Ln(3+)结合位点的四甲基丙二酰胺(TMMA)基团。传感器对镧系离子的比色响应是即时的,对于 Eu(3+)和 Sm(3+),其灵敏度低至约 50 nM。这项研究展示了一种直接、方便的纳米粒子合成的通用策略,该策略能够将分析物结合基团直接掺入纳米粒子表面,从而可以开发用于广泛应用的比色传感器。一步合成提供了均匀的表面配体组成,减少了纳米粒子合成和纯化过程中产生的废物量,生成了在非修饰的水相环境中稳定的功能化金纳米粒子,并在环境温度下提供比色检测。

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