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Oxoanion recognition by benzene-based tripodal pyrrolic receptors

Authors
Bill, Nathan L.Kim, Dae-SikKim, Sung KukPark, Jung SuLynch, Vincent M.Young, Neil J.Hay, Benjamin P.Yang, YoujunAnslyn, Eric V.Sessler, Jonathan L.
Issue Date
Jan-2012
Publisher
TAYLOR & FRANCIS LTD
Keywords
anion receptors; dihydrogen phosphate; hydrogen sulphate; theoretical calculations; X-ray structure
Citation
SUPRAMOLECULAR CHEMISTRY, v.24, no.1, pp 72 - 76
Pages
5
Journal Title
SUPRAMOLECULAR CHEMISTRY
Volume
24
Number
1
Start Page
72
End Page
76
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/147675
DOI
10.1080/10610278.2011.622392
ISSN
1061-0278
1029-0478
Abstract
Two new tripodal receptors based on pyrrole-and dipyrromethane-functionalised derivatives of a sterically geared precursor, 1,3,5-tris(aminomethyl)-2,4,6-triethylbenzene, are reported; these systems, compounds 1 and 2, display high affinity and selectivity for tetrahedral anionic guests, in particular dihydrogen phosphate, pyrophosphate and hydrogen sulphate, in acetonitrile as inferred from isothermal titration calorimetry measurements. Support for the anion-binding ability of these systems comes from theoretical calculations and a single-crystal X-ray diffraction structure of the 2:2 (host:guest) dihydrogen phosphate complex is obtained in the case of the pyrrole-based receptor system, 1.
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