Constraining Homo- and Heteroanion Dimers in Ultraclose Proximity within a Self-Assembled Hexacationic Cage
- Authors
- Wang, Hongye; Fang, Shuai; Wu, Guangcheng; Lei, Ye; Chen, Qiong; Wang, Hongliang; Wu, Yating; Lin, Chuhao; Hong, Xin; Kim, Sung Kuk; Sessler, Jonathan L.; Li, Hao
- Issue Date
- 25-Nov-2020
- Publisher
- American Chemical Society
- Citation
- Journal of the American Chemical Society, v.142, no.47, pp 20182 - 20190
- Pages
- 9
- Indexed
- SCIE
SCOPUS
- Journal Title
- Journal of the American Chemical Society
- Volume
- 142
- Number
- 47
- Start Page
- 20182
- End Page
- 20190
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/5914
- DOI
- 10.1021/jacs.0c10253
- ISSN
- 0002-7863
1520-5126
- Abstract
- A hexacationic cage 3(6+) was synthesized via hydrazone condensation in aqueous acid. Cage 3(6+) bears three biscationic arms, each of which contains four relatively acidic protons, including one NH and three CH protons. These hydrogen bond donors, as well as its intrinsic cationic nature, enable cage 3(6+) to encapsulate two anions concurrently within its cavity. The axial asymmetrical nature of the biscationic arms allow the cage to recognize two different anions in a selective manner, to encompass bound heteroanion dimers, such as Cl-center dot NO3(-) and Cl-center dot Br-. Single crystal X-ray diffraction analyses reveal that in the solid state the two anions are constrained in ultraclose proximity within the cage; e.g., the Cl-center dot center dot center dot Cl- and Cl-center dot center dot center dot Br- distances are 3.2 and 2.9 angstrom, respectively, which are shorter than the sum of their van der Waals radii. Evidence consistent with the sequential binding of two identical or disparate anions in CD3CN is also presented.
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