| Literature DB >> 28799691 |
Mohamed Hifsudheen1,2, Rakesh K Mishra1, Balaraman Vedhanarayanan1,2, Vakayil K Praveen1,2, Ayyapanpillai Ajayaghosh1,2.
Abstract
Higher-order super-helical structures derived from biological molecules are known to evolve through opposite coiling of the initial helical fibers, as seen in collagen protein. A similar phenomenon is observed in a π-system self-assembly of chiral oligo(phenyleneethylene) derivatives (S)-1 and (R)-1 that explains the unequal formation of both left- and right-handed helices from molecule having a specific chiral center. Concentration- and temperature-dependent circular dichroism (CD) and UV/Vis spectroscopic studies revealed that the initial formation of helical aggregates is in accordance with the molecular chirality. At the next level of hierarchical self-assembly, coiling of the fibers occurs with opposite handedness, thereby superseding the command of the molecular chirality. This was confirmed by solvent-dependent decoiling of super-helical structures and concentration-dependent morphological analysis.Entities:
Keywords: chirality; circular dichroism; helical structures; self-assembly; π-systems
Year: 2017 PMID: 28799691 DOI: 10.1002/anie.201707392
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336