4.3 Article

Optical and electrochemical properties of tunable host-guest complexes linked to plasmonic interfaces

Journal

JOURNAL OF MATERIALS CHEMISTRY
Volume 21, Issue 9, Pages 3006-3013

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c0jm03293j

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Funding

  1. EU-FEDER and Interreg IV
  2. Centre National de la Recherche Scientifique (CNRS)
  3. Nord-Pas-de Calais region
  4. Agence Nationale de la Recherche [ANR-09-JCJC-0032-01]

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This article describes the use of localized surface plasmon resonance (LSPR) interface to detect complexation/decomplexation steps of a controllable host-guest system at the solid-liquid interface. The LSPR interfaces consist of a sandwiched structure comprising a tin-doped indium oxide (ITO) substrate, gold nanostructures (Au NSs) and a thin ITO film overcoating. Click chemistry was used to covalently link an alkyne-functionalized pi-electron deficient tetracationic cyclophane cyclobis(paraquat-p-phenylene) (CBPQT(4+)) unit to an azide-terminated LSPR interface. The modified interfaces were characterized using X-ray photoelectron spectroscopy (XPS), cyclic voltammetry and UV-vis transmission spectroscopy. Tetrathiafulvalene (TTF) was used as a model guest molecule to demonstrate the possibility to follow the complexation/decomplexation events by monitoring the change in the LSPR signal. The results demonstrate that redox controlled host-guest complexation at the surface can be monitored effectively using LSPR.

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