4.7 Article

Cucurbit[8]uril-mediated pseudo[2,3]rotaxanes

Journal

CHEMICAL COMMUNICATIONS
Volume 55, Issue 88, Pages 13227-13230

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c9cc07144j

Keywords

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Funding

  1. Leverhulme Trust
  2. EPSRC [EP/R013012/1, EP/N020669/1, EP/L027151/1]
  3. BBSRC [BB/N007700/1]
  4. ERC Starting Grant (BioNet) [757850]
  5. ERC-2016 Consolidator Grant (CAM-RIG) [726470]
  6. BBSRC [BB/N007700/1] Funding Source: UKRI
  7. EPSRC [EP/N020669/1, EP/L027151/1, EP/R013012/1] Funding Source: UKRI
  8. European Research Council (ERC) [726470] Funding Source: European Research Council (ERC)

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Pseudo[2,3]rotaxanes have been successfully fabricated by the complexation of cucurbit[8]uril (CB[8]) macrocycles with extended viologen derivatives. Two design rules enable the incorporation of a third CB[8] onto a recently reported pseudo[2,2]rotaxane. Incorporation of a third macrocycle confines the dimeric stacking of chromophores into specific alignment, leading to effective electron-delocalisation along their long molecular axis.

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