Abstract

Creating well-defined plasmonic hotspots with enormous field enhancements as well as the capability of selectively trapping targeted molecules into hotspots is of critical importance and a prerequisite for numerous plasmon-assisted applications, but it represents a great challenge. In this work, a robust molecular cage decorated with thioether moieties at the periphery was designed and synthesized. By using the synthesized cage as a linker, a series of molecular cage-bridged plasmonic structures with well-defined nanogaps (hotspots) were fabricated in an efficient and controllable fashion. It was found both experimentally and theoretically that the nanogaps of about 1.2 nm created by the molecular cage in the resultant plasmonic structures led to a strong plasmon coupling, thus inducing great field enhancement inside the nanogaps. More importantly, the embedded molecular cages endowed the formed hotspots with the capability of selectively trapping targeted molecules, offering huge opportunities for many emergent applications. As a demonstration, the hotspots constructed were used as a unique nanoreactor, and under mild conditions two types of plasmon-driven chemical transformation were successfully performed. All the results clearly indicate that the integration of the host-guest chemistry of the molecular cage with the plasmon-coupling effect of metal particles afforded a new class of plasmonic structures, showing great potential for facilitating a broad variety of plasmon-based applications.

Highlights

  • Noble metal nanoparticles (NPs) support unique localized surface plasmon resonances (LSPRs) through coherent oscillations of free electrons in metallic nanostructures under light illumination, and a strong electromagnetic eld is induced in the close vicinity of the metal surface.[1]

  • Similar results were observed for the case of the cycloaddition reaction (Fig. S35†). These results clearly indicate that the use of the Pd2L4 molecular cage can efficiently generate the highly desired plasmonic hotspots with small (1.2 nm) separation, but can simultaneously impart the capability of trapping low affinity guests in the created hotspots, which could greatly expand the applications of plasmon-assisted chemistry

  • Creating well-de ned plasmonic hotspots with enormous eld enhancement as well as the capability of selectively trapping targeted molecules into hotspots is critical for numerous plasmon-assisted applications, but represents a great challenge

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Summary

Introduction

Noble metal nanoparticles (NPs) support unique localized surface plasmon resonances (LSPRs) through coherent oscillations of free electrons in metallic nanostructures under light illumination, and a strong electromagnetic eld is induced in the close vicinity of the metal surface.[1]. Based on this preliminary result, in our work, to achieve well-de ned cluster structures, the controlled assembly of Au NPs and the molecular cage was performed in discrete microdroplets in a micro uidic device (Fig. S22†).

Results
Conclusion
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