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Structural and Molecular Recognition Studies with Acyclic Anion Receptors
Abstract
Acyclic molecules containing amides, ureas, and pyrrole groups have proven to be effective and selective anion-binding agents. In this Account, the structural chemistry of isophthalamide anion complexes, ortho-phenylenediamine based bis-ureas, and amidopyrroles, as well as anion-triggered deprotonation processes in neutral anion receptor systems, are discussed.
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Cited by
A new trend in rhodamine-based chemosensors: application of spirolactam ring-opening to sensing ions
Kim, H. N., Lee, M. H., Kim, H. J., Kim, J. S., & Yoon, J. (2008) · Chemical Society Reviews · doi:10.1039/b802497a · Cited by 1,649
Sensors for the optical detection ofcyanide ion
Xu, Z., Chen, X., Kim, H. N., & Yoon, J. (2010) · Chem. Soc. Rev. · doi:10.1039/b907368j · Cited by 1,121
Recognition and sensing of fluoride anion
Cametti, M., & Rissanen, K. (2009) · Chemical Communications · doi:10.1039/b902069a · Cited by 654
Metadata
- Authors
- Gale, P. A.
- Venue
- Accounts of Chemical Research
- Publisher
- American Chemical Society (ACS)
- Published
- 2006-05-26
- Volume
- 39
- Issue
- 7
- Pages
- 465-475
- ISSN
- 0001-4842 (ISSN-L)
- 1520-4898
- OpenAlex
- W2139335926
- Cited by
- 681
- References
- 0
- FWCI
- 43.07
- Type
- journal article
- Language
- en
- Open access
- closed
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- Gale, P. A. (2006). Structural and Molecular Recognition Studies with Acyclic Anion Receptors. Accounts of Chemical Research. https://doi.org/10.1021/ar040237q
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