Abstract
[structure: see text] Screening of a bead-supported encoded library of unnatural polyamines against model polyanionic targets (1 and 2) demonstrated that a combinatorial approach can highlight structural selectivity in multivalent ion pairing in aqueous solutions. This approach even provided -NH-2Acc(R)-6Ahx(R)-Et, a highly target-selective triamine sequence that can discriminate between two trisulfonated dyes displaying subtle structural differences.
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