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Updated: May 22, 2026

Synthesis of Information-bearing Peptoids and their Sequence-directed Dynamic Covalent Self-assembly
Published on: February 6, 2020
Stoichiometric self-assembly of isomeric, shape-persistent, supramacromolecular bowtie and butterfly structures
Anthony Schultz1, Xiaopeng Li, Balaka Barkakaty
1Department of Chemistry, The University of Akron, Akron, Ohio 44325, USA.
Abstract:
Two novel macromolecular constitutional isomers have been self-assembled from previously unreported terpyridine ligands in a three-component system. The terpyridine ligands were synthesized in high yields via a key Suzuki coupling. Restrictions of the possible outcomes for self-assembly ultimately provided optimum conditions for isolation of either a molecular bowtie or its isomeric butterfly motif. These isomers have been characterized by ESI-MS, TWIM-MS, (1)H NMR, and (13)C NMR. Notably, these structural isomers have remarkably different drift times in ion mobility separation, corresponding to different sizes and shapes at high charge states.
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