| Literature DB >> 27383466 |
Martin J Hollamby1, Keisuke Aratsu2, Brian R Pauw3, Sarah E Rogers4, Andrew J Smith5, Mitsuaki Yamauchi2, Xu Lin2, Shiki Yagai6.
Abstract
Molecular self-assembly primarily occurs in solution. To better understand this process, techniques capable of probing the solvated state are consequently required. Small-angle scattering (SAS) has a proven ability to detect and characterize solutions, but it is rarely applied to more complex assembly shapes. Here, small-angle X-ray and neutron scattering are applied to observe toroidal assemblies in solution. Combined analysis confirms that the toroids have a core-shell structure, with a π-conjugated core and an alkyl shell into which solvent penetrates. The dimensions determined by SAS agree well with those obtained by (dried-state) atomic force microscopy. Increasing the number of naphthalene units in the molecular building block yields greater rigidity, as evidenced by a larger toroid and a reduction in solvent penetration into the shell. The detailed structural analysis demonstrates the applicability of SAS to monitor complex solution-based self-assembly.Entities:
Keywords: nanorings; self-assembly; small-angle scattering; supramolecular chemistry; toroids
Year: 2016 PMID: 27383466 DOI: 10.1002/anie.201603370
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336