Acridinium Ester-Functionalized Carbon Nanomaterials: General Synthesis Strategy and Outstanding Chemiluminescence.

Abstract

In this work, three different kinds of acridinium ester (AE)-functionalized carbon nanomaterials, including AE-functionalized carbon nanoparticles (AE-CNPs), AE-functionalized graphene oxide (AE-GO), and AE-functionalized multiwalled carbon nanotubes (AE-MCNTs), were synthesized for the first time via a simple, general, and noncovalent strategy. AE molecules were assembled on the surface of carbon nanomaterials by electrostatic interaction, π-π stacking interaction, and amide bond. The synthesized AE-CNPs, AE-GO, and AE-MCNTs with 5.0 × 10(-8) mol·L(-1) of synthetic AE concentration, which was very low compared with other chemiluminescence (CL) reagents such as luminol, N-(aminobutyl)-N-(ethylisoluminol), and lucigenin at the concentration of 3.3 × 10(-4) to 5.0 × 10(-6) mol·L(-1) used for the synthesis of CL-functionalized nanomaterials, exhibited outstanding CL activity and good stability. It was found that carbon nanomaterials as nanosized platforms could efficiently immobilize AE molecules and facilitate the formation of OH(•) and O2(•-), leading to strong light emission. Moreover, the CL intensity of AE-GO was the highest, which was about 8.7 and 3.7 times higher than that of AE-CNPs and AE-MCNTs, respectively. This mainly resulted from a difference in the amount of adsorbed AE molecules on the surface of different carbon nanomaterials. Additionally, the prepared AE-CNPs demonstrated excitation-dependent fluorescence property and good fluorescence stability against photobleaching. On the basis of the excellent CL and special fluorescence properties of AE-CNPs, a dual-mode array strategy has been proposed for the first time and seven kinds of transition-metal ions could be successfully discriminated.