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The cucurbit[n]uril family:: Prime components for self-sorting systems

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JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 127, 期 45, 页码 15959-15967

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AMER CHEMICAL SOC
DOI: 10.1021/ja055013x

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  1. NIGMS NIH HHS [GM61854] Funding Source: Medline

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We determined the values of K-a for a wide range of host-guest complexes of cucurbit[n]uril (CB[n]), where n = 6-8, using H-1 NMR competition experiments referenced to absolute binding constants measured by UV/vis titration. We find that the larger homologues-CB[7] and CB[8]-individually maintain the size, shape, and functional group selectivity that typifies the recognition behavior of CB[6]. The cavity of CB[7] is found to effectively host trimethylsilyl groups. Remarkably, the values of Ka for the interaction of CB[7] with adamantane derivatives 22-24 exceeds 10(12) M-1! The high levels of selectivity observed for each CB[n] individually is also observed for the CB[n] family collectively. That is, the selectivities of CB[6], CB[7], and CB[8] toward a common guest can be remarkably large. For example, guests 1, 3, and 11 prefer CB[8] relative to CB[7] by factors greater than 10(7), 10(6), and 3000, respectively. Conversely, guests 23 and 24 prefer CB[7] relative to CB[8] by factors greater than 5100 and 990, respectively. The high levels of selectivity observed individually and collectively for the CB[n] family renders them prime components for the preparation of functional biomimetic self-sorting systems.

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