4.8 Article

Triple Stack of a Viologen Derivative in a CB[10] Pair

Journal

ORGANIC LETTERS
Volume 23, Issue 14, Pages 5283-5287

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.1c00773

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Funding

  1. Wuhan University of Science and Technology (WUST)
  2. CNRS
  3. NSFC [21871216]
  4. Aix-Marseille Universite

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A viologen-phenylene-imidazole (VPI) conjugate can form antiparallel triple stacks in water with cucurbit[10]uril (CB[10]), pairwise complexing the guest trimer. The quinary host:guest 2:3 complex displays features assignable to charge-transfer interactions, and under reductive conditions, CB[10] can solubilize a VPI radical.
A viologen-phenylene-imidazole (VPI) conjugate, previously shown to be singly complexed by CB[7] and doubly bound by CB[8], is herein shown to form antiparallel triple stacks in water with cucurbit[10]uril (CB[10]), pairwise complexing the guest trimer. The quinary host:guest 2:3 complex showed features assignable to charge-transfer interactions. Under reductive conditions, CB[10] could solubilize a VPI radical, even though CB[10] and reduced VPI are almost insoluble, thereby illustrating a possible new application for CB[10].

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