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石墨烯基片作为相互作用分子的发射和振动响应的修饰剂:BODIPY 染料的情况。

Graphenic substrates as modifiers of the emission and vibrational responses of interacting molecules: The case of BODIPY dyes.

机构信息

Unidad Académica de Física, Universidad Autónoma de Zacatecas, 98068 Zacatecas, México; Instituto de Ciencias Aplicadas y Tecnología, Universidad Nacional Autónoma de México, Circuito exterior S/N, Ciudad Universitaria, 04510 Ciudad de Mexico, México.

Instituto de Ciencias Nucleares, Universidad Nacional Autónoma de México, Circuito exterior S/N, Ciudad Universitaria, 04510 Ciudad de Mexico. México.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2021 Feb 5;246:119020. doi: 10.1016/j.saa.2020.119020. Epub 2020 Oct 5.

DOI:10.1016/j.saa.2020.119020
PMID:33075704
Abstract

Graphenic substrates (GS), such as reduced graphene oxide (rGO) and graphene oxide (GO), are 2D materials known for their unique physicochemical properties such as their ability to enhance vibrational spectroscopic signals and quench the fluorescence of adsorbed molecules. These properties provide an opportunity to develop nanostructured GS-based systems for detecting and identifying different analytes with high sensitivity and reliability through molecular spectroscopic techniques. This work evaluated the capacities of different GS to interact with a highly fluorescent compound, thereby changing its optical emission response (fluorescence quenching) and amplifying its vibrational signal, which is the base of graphene-enhanced Raman scattering (GERS). To test these properties, we used a derivative of highly fluorescent BODIPY (BP) compounds, which cover a wide range of applications from solar energy conversion to photodynamic cancer therapy. GS prepared by using the Langmuir-Blodgett (LB) technique allowed us to quench the fluorescence emission of BP and improve its Raman spectroscopy detection limit due to the GERS effect. These results were interpreted in light of the π-π interactions taking place between the Csp domains of GS and the aromatic core of the BP fluorophore.

摘要

石墨烯基底物(GS),如还原氧化石墨烯(rGO)和氧化石墨烯(GO),是具有独特物理化学性质的二维材料,其能够增强振动光谱信号并猝灭吸附分子的荧光就是其性质之一。这些性质为通过分子光谱技术开发用于检测和识别不同分析物的基于纳米结构 GS 的系统提供了机会,其具有高灵敏度和可靠性。本工作评估了不同 GS 与高荧光化合物相互作用的能力,从而改变其光学发射响应(荧光猝灭)并放大其振动信号,这是石墨烯增强拉曼散射(GERS)的基础。为了测试这些性质,我们使用了高度荧光 BODIPY(BP)化合物的衍生物,其应用范围广泛,从太阳能转换到光动力癌症治疗。使用 Langmuir-Blodgett(LB)技术制备的 GS 允许我们猝灭 BP 的荧光发射,并由于 GERS 效应提高其拉曼光谱检测限。这些结果根据 GS 的 Csp 域与 BP 荧光团的芳环核心之间发生的π-π相互作用进行了解释。

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