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Synthesis of Pillar[5]arene Dimers and Their Cooperative Binding toward Some Neutral Guests

Li, Chunju, Han, Kang, Li, Jian, Zhang, Haichang, Ma, Junwei, Shu, Xiaoyan, Chen, Zhenxia, Weng, Linhong, Jia, Xueshun·2012·Organic Letters

Abstract

Three pillar[5]arene dimers, bridged by a flexible aliphatic chain (H1) or a relatively rigid phenylene unit (H2 and H3), were synthesized, with the possible synthetic strategies being discussed. The dimers could significantly enhance the binding affinities toward neutral model substrates in comparison with monomeric 1,4-dimethoxypillar[5]arene (H4) through the cooperative binding of two pillar[5]arene moieties. The molecular binding ability and selectivity are discussed from the viewpoints of the size/shape-fit concept and multiple recognition mechanism.

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Metadata

Authors
Li, C., Han, K., Li, J., Zhang, H., Ma, J., Shu, X., Chen, Z., Weng, L., & Jia, X.
Venue
Organic Letters
Published
2011-12-05
Volume
14
Issue
1
Pages
42-45
ISSN
  • 1523-7052 (ISSN-L)
  • 1523-7060
OpenAlex
W2328918411
Cited by
158
References
0
FWCI
10.17
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Synthesis of Pillar[5]arene Dimers and Their Cooperative Binding toward Some Neutral Guests. https://app.cochat.ai/papers/10.1021/ol2027834
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Li, C., Han, K., Li, J., Zhang, H., Ma, J., Shu, X., Chen, Z., Weng, L., & Jia, X. (2012). Synthesis of Pillar[5]arene Dimers and Their Cooperative Binding toward Some Neutral Guests. Organic Letters. https://doi.org/10.1021/ol2027834

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.