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Supramolecular Double Helices from Small C3-Symmetrical Molecules Aggregated in Water

R. P. M. Lafleur, S. Herziger, S. M. C. Schoenmakers, A. D. A. Keizer, J. Jahzerah, B. N. S. Thota, L. Su, P. H. H. Bomans, N. A. J. M. Sommerdijk, A. R. A. Palmans, R. Haag, H. Friedrich, C. Böttcher and E. W. Meijer – 2020

Supramolecular fibers in water, micrometers long and several nanometers in width, are among the most studied nanostructures for biomedical applications. These supramolecular polymers are formed through a spontaneous self-assembly process of small amphiphilic molecules by specific secondary interactions. Although many compounds do not possess a stereocenter, recent studies suggest the (co)existence of helical structures, albeit in racemic form. Here, we disclose a series of supramolecular (co)polymers based on water-soluble benzene-1,3,5-tricarboxamides (BTAs) that form double helices, fibers that were long thought to be chains of single molecules stacked in one dimension (1D). Detailed cryogenic transmission electron microscopy (cryo-TEM) studies and subsequent three-dimensional-volume reconstructions unveiled helical repeats, ranging from 15 to 30 nm. Most remarkable, the pitch can be tuned through the composition of the copolymers, where two different monomers with the same core but different peripheries are mixed in various ratios. Like in lipid bilayers, the hydrophobic shielding in the aggregates of these disc-shaped molecules is proposed to be best obtained by dimer formation, promoting supramolecular double helices. It is anticipated that many of the supramolecular polymers in water will have a thermodynamic stable structure, such as a double helix, although small structural changes can yield single stacks as well. Hence, it is essential to perform detailed analyses prior to sketching a molecular picture of these 1D fibers.

Titel
Supramolecular Double Helices from Small C3-Symmetrical Molecules Aggregated in Water
Verfasser
R. P. M. Lafleur, S. Herziger, S. M. C. Schoenmakers, A. D. A. Keizer, J. Jahzerah, B. N. S. Thota, L. Su, P. H. H. Bomans, N. A. J. M. Sommerdijk, A. R. A. Palmans, R. Haag, H. Friedrich, C. Böttcher and E. W. Meijer
Datum
2020
Kennung
DOI:10.1021/jacs.0c08179
Zitierweise
J Am Chem Soc 2020, 142 (41), 17644-17652
Sprache
eng
Art
Text