Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 142, Issue 26, Pages 11404-11416Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jacs.0c00707
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Funding
- Marie Sklodowska-Curie Actions [PITN-GA-2010-264699, H2020-MSCA-ETN-2016, 722171]
- Swedish Vetenskapsradet (VR) [2014-3794]
- Deutsche Forschungsgemeinsc haft (DFG) [Se 777/9-1]
- Sweden Knowledge-Foundation (KKS) [20150086]
- Marie Curie Actions (MSCA) [722171] Funding Source: Marie Curie Actions (MSCA)
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The design of artificial oxyanion receptors with switchable ion preference is a challenging goal in host-guest chemistry. We here report on molecularly imprinted polymers (MIPs) with an external phospho-sulpho switch driven by small molecule modifiers. The polymers were prepared by hydrogen bond-mediated imprinting of the mono- or dianions of phenyl phosphonic acid (PPA), phenyl sulfonic acid (PSA), and benzoic acid (BA) using N-3,5-bis-(trifluoromethyl)-phenyl-N-4-vinyl-phenyl urea (1) as the functional host monomer. The interaction mode between the functional monomer and the monoanions was elucidated by H-1 NMR titrations and H-1-H-1 NMR NOESY supported by molecular dynamic simulation, which confirmed the presence of high-order complexes. PPA imprinted polymers bound PPA with an equilibrium constant K-eq = 1.8 x 10(5) M-1 in acetonitrile (0.1% 1,2,2,6,6-pentamethylpiperidine) and inorganic HPO42- and SO42- with K-eq = 2.9 X 10(3) M-1 and 4.5 X 10(3) M-1, respectively, in aqueous buffer. Moreover, the chromatographic retentivity of phosphonate versus sulfonate was shown to be completely switched on this polymer when changing from a basic to an acidic modifier. Mechanistic insights into this system were obtained from kinetic investigations and DSC-, MALDI-TOF-MS-, H-1 NMR-studies of linear polymers prepared in the presence of template. The results suggest the formation of template induced 1-1 diad repeats in the polymer main chain shedding unique light on the relative contributions of configurational and conformational imprinting.
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