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Supramolecular Click Chemistry for Surface Modification of Quantum Dots Mediated by Cucurbit[7]uril.
McGuire, Katie; He, Suhang; Gracie, Jennifer; Bryson, Charlotte; Zheng, Dazhong; Clark, Alasdair W; Koehnke, Jesko; France, David J; Nau, Werner M; Lee, Tung-Chun; Peveler, William J.
Afiliación
  • McGuire K; School of Chemistry, Joseph Black Building, University of Glasgow, Glasgow, G12 8QQ, United Kingdom.
  • He S; School of Science, Constructor University, Campus Ring 1, 28759 Bremen, Germany.
  • Gracie J; School of Chemistry, Joseph Black Building, University of Glasgow, Glasgow, G12 8QQ, United Kingdom.
  • Bryson C; School of Chemistry, Joseph Black Building, University of Glasgow, Glasgow, G12 8QQ, United Kingdom.
  • Zheng D; School of Chemistry, Joseph Black Building, University of Glasgow, Glasgow, G12 8QQ, United Kingdom.
  • Clark AW; James Watt School of Engineering, Advanced Research Centre, University of Glasgow, Glasgow, G11 6EW, United Kingdom.
  • Koehnke J; School of Chemistry, Joseph Black Building, University of Glasgow, Glasgow, G12 8QQ, United Kingdom.
  • France DJ; Institut für Lebensmittelchemie, Leibniz Universität Hannover, Callinstr 5, 30167 Hannover, Germany.
  • Nau WM; School of Chemistry, Joseph Black Building, University of Glasgow, Glasgow, G12 8QQ, United Kingdom.
  • Lee TC; School of Science, Constructor University, Campus Ring 1, 28759 Bremen, Germany.
  • Peveler WJ; Institute for Materials Discovery, University College London, London, WC1H 0AJ, United Kingdom.
ACS Nano ; 17(21): 21585-21594, 2023 Nov 14.
Article en En | MEDLINE | ID: mdl-37922402
Cucurbiturils (CBs), barrel-shaped macrocyclic molecules, are capable of self-assembling at the surface of nanomaterials in their native state, via their carbonyl-ringed portals. However, the symmetrical two-portal structure typically leads to aggregated nanomaterials. We demonstrate that fluorescent quantum dot (QD) aggregates linked with CBs can be broken-up, retaining CBs adsorbed at their surface, via inclusion of guests in the CB cavity. Simultaneously, the QD surface is modified by a functional tail on the guest, thus the high affinity host-guest binding (logKa > 9) enables a non-covalent, click-like modification of the nanoparticles in aqueous solution. We achieved excellent modification efficiency in several functional QD conjugates as protein labels. Inclusion of weaker-binding guests (logKa = 4-6) enables subsequent displacement with stronger binders, realising modular switchable surface chemistries. Our general "hook-and-eye" approach to host-guest chemistry at nanomaterial interfaces will lead to divergent routes for nano-architectures with rich functionalities for theranostics and photonics in aqueous systems.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: ACS Nano Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: ACS Nano Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Estados Unidos