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Propensity for local folding induced by the urea fragment in short-chain oligomers

2008; Royal Society of Chemistry; Volume: 6; Issue: 14 Linguagem: Inglês

10.1039/b801139g

1477-0539

Lucile Fischer, Claude Didierjean, Franck Jolibois, Vincent Semetey, José Manuel Lozano, Jean‐Paul Briand, Michel Marraud, Romuald Poteau, Gilles Guichard,

Click Chemistry and Applications

Examination of local folding and H-bonding patterns in model compounds can be extremely informative to gain insight into the propensity of longer-chain oligomers to adopt specific folding patterns (i.e. foldamers) based on remote interactions. Using a combination of experimental techniques (i.e.X-ray diffraction, FT-IR absorption and NMR spectroscopy) and theoretical calculations at the density functional theory (DFT) level, we have examined the local folding patterns induced by the urea fragment in short-chain aza analogues of β- and γ-amino acid derivatives. We found that the urea-turn, a robust C8 conformation based on 1←3 H-bond interaction, is largely populated in model ureidopeptides (I–IV) obtained by replacing the α-carbon of a β-amino acid by a nitrogen. This H-bonding scheme is likely to compete with remote H-bond interactions, thus preventing the formation of secondary structures based on remote intrastrand interactions in longer oligomers. In related oligomers obtained by the addition of a methylene in the main chain (V–VIII), nearest-neighbour H-bonded interactions are unfavourable i.e. the corresponding C9 folding pattern is hardly populated. In this series, folding based on remote intrastrand interactions becomes possible for longer oligomers. We present spectroscopic evidence that tetraurea VIII is likely to be the smallest unit capable of reproducing the H-bonded motif found in 2.5-helical N,N′-linked oligoureas.