4.8 Article

[2]Pseudorotaxanes from T-Shaped Benzimidazolium Axles and [24]Crown-8 Wheels

Journal

ORGANIC LETTERS
Volume 14, Issue 10, Pages 2484-2487

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol300761q

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Funding

  1. NSERC of Canada
  2. FQRNT (Quebec)
  3. ICDD

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A new templating motif for the formation of [2]pseudorotaxanes is described in which T-shaped axles with a benzimidazolium core and aromatic substituents at the 2-, 4-, and 7-positions interact with [24]crown-8 ether wheels ([24]crown-8, dibenzo[24]crown-8, and dinaphtho[24]crown-8). The T-shape greatly enhances the association between axle and wheel when compared to simple imidazolium or benzimidazolium cations. A series of interpenetrated molecules are characterized by H-1 NMR spectroscopy and single crystal X-ray crystallography.

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