4.8 Article

Ex2Box: Interdependent Modes of Binding in a Two-Nanometer-Long Synthetic Receptor

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 135, Issue 34, Pages 12736-12746

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja4052763

Keywords

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Funding

  1. Non-Equilibrium Energy Research Center (NERC), an Energy Frontier Research Center (EFRC) - U.S. Department of Energy, Office of Basic Energy Sciences (DOE-BES) [DESC0000989]
  2. The Netherlands Organization for Scientific Research (NWO)
  3. Marie Curie Cofund Action (Rubicon Fellowship)
  4. Department of Defense (DoD) [32 CFR 168a]
  5. NU International Institute for Nano-technology (IIN)
  6. National Science Foundation (NSF)

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Incorporation of two biphenylene-bridged 4,4'-bipyridinium extended viologen units into a para-phenylene-based cyclophane results in a synthetic receptor that is similar to 2 m long and adopts a box-like geometry. This cyclophane, Ex(2)Box(4+), possesses the ability to form binary and ternary complexes with a myriad of guest molecules ranging from long pi-electron-rich polycyclic aromatic hydrocarbons, such as tetracene, tetraphene, and chrysene, to pi-electron-poor 2,6-dinitrotoluene, 1,2,4-trichlorobenzene, and both the 9,10- and 1,4-anthraquinone molecules. Moreover, Ex(2)Box(4+) is capable of forming one-to-one complexes with polyether macrocycles that consist of two pi-electron-rich dioxynaphthalene units, namely, 1,5-dinaphtho[38]-crown-10. This type of broad molecular recognition is possible because the electronic constitution of Ex(2)Box(4+) is such that the pyridinium rings located at the ends of the cyclophane are electron-poor and prefer to enter into donor acceptor interactions with pi-electron-rich guests, while the middle of the cyclophane, consisting of the biphenylene spacer, is more electron-rich and can interact with pi-electron-poor guests. In some cases, these different modes of binding can act in concert to generate one-to-one complexes which possess high stability constants in organic media. The binding affinity of Ex(2)Box(4+) was investigated in the solid state by way of single-crystal X-ray diffraction and in solution by using UV-vis and NMR spectroscopy for 12 inclusion complexes consisting of the tetracationic cyclophane and the corresponding guests of different sizes, shapes, and electronic compositions. Additionally, density functional theory was carried out to elucidate the relative energetic differences between the different modes of binding of Ex(2)Box(4+) with anthracene, 9,10-anthraquinone, and 1,4-anthraquinone in order to understand the degree with which each mode of binding contributes to the overall encapsulation of each guest.

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