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Mechanistic study demonstrates a two-stage topochemical reaction in a peptide xerogel lattice, highlighting a pathway to synthesize pseudopolypeptides from non-crystalline aggregates.
Difficult peptides, particularly those enriched in β-branched hydrophobic residues, readily aggregate but often resist crystallization, limiting their use as substrates for topochemical synthesis. Here, we show that a β-sheet xerogel (XG) derived from a homochiral valine dipeptide provides a highly ordered supramolecular framework that supports an unprecedented two-stage topochemical azide-alkyne cycloaddition. Mild heating (70°C) induces quantitative, regiospecific monomer-to-dimer conversion with sigmoidal kinetics while preserving the cross-β architecture. This first topochemical reaction generates an ordered dimer phase that, upon further heating (160°C), undergoes a second sigmoidal topochemical reaction in which the dimer becomes the operative reactive repeat unit, affording a regiospecific 1,4-triazole-linked pseudopolypeptide. Differential scanning calorimetry (DSC) reveals two discrete exotherms that are consumed sequentially, while time-resolved PXRD shows evolution of the reaction lattice with retention of the characteristic cross-β reflections, albeit with changes in the longer-range diffraction features. Fourier transform infrared (FT-IR) spectroscopy further supports preservation of the hydrogen-bonded β-sheet framework throughout both transformations. Together, these observations reveal a mechanism in which the β-sheet framework persists while the supramolecular structure reorganizes, redefining the reactive periodicity from monomer to dimer.
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Sebastián et al. (2026) studied this question.
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