Vybornyi, MykhailoMykhailoVybornyiHäner, RobertRobertHäner0000-0001-5014-43182024-10-232024-10-232014-09-11https://boris-portal.unibe.ch/handle/20.500.12422/126654Herein we demonstrate that a substitution type of the pyrene in short amphiphilic oligomers determines a morphology of the assemblies formed. Thus, 1.6- and 2.7-linkages lead to a formation of micrometer-sized 2D supromolecular polymers with a constant thickness 2 nm (pictures A and B). These assemblies possess a high degree of an internal order: the interior consists of hydrophobic pyrenes and alkyl chains, whereas the exterior exists as a net of hydrophilic negatively charged phosphates. Contrary, a 1.8-linkage exclusiveley leads to a formation of long nanometer thick helical supramolecular polymers (picturee C). These structures tend to form even more complex assemblies (bundles, superhelixes). Moreover, for all samples the polymerization process occurs via a nucleation-elongation mechanism. To study Py3 self-assembly, we carried out whole set of spectroscopic (UV/vis, fluorescence, DLS) and microscopic experiments (AFM).en500 - Science::570 - Life sciences; biology500 - Science::540 - ChemistryDiversity of morphological patterns in supramolecular polymers formed from the amphiphilic oligomers of pyrenesconference_item10.7892/boris.58922