Nature Communications · 2018 · 51 citations · 51 references
Natural SciencesChemistryMaterials ScienceMaterials ChemistryNanomaterialsSolid-state ChemistryOrganic Electronic MaterialsOrganic SemiconductorsSelf-assembled MaterialsSelf-assembled NanostructuresSelf-assemblySelf-assembly Of NanomaterialsCo-assemblyConjugated MoleculesCore-shell NanostructuresEpitaxial Growth KineticsGrowth KineticsOrganic Self-assemblySmall-molecule Organic SemiconductorsSmall-molecule Semiconductors
Abstract Integrating together two dissimilar π-conjugated molecules into controlled complex topological configurations remains a largely unsolved problem owing to the diversity of organic species and their respective different assembly features. Here, we find that two structurally similar organic semiconductors, 9,10-bis(phenylethynyl)anthracene (BA) and 5,12-bis(phenylethynyl)naphthacene (BN), co-assemble into two-component helices by control of the growth kinetics as well as the molar ratio of BA/BN. The helical superstructures made of planar and twisted bis(phenylethynyl) derivatives can be regarded as (BA) x (BN) 1− x alloys, which are formed due to compatible structural relationship between BA and BN. Moreover, epitaxial growth of (BA) x (BN) 1− x alloy layer on the surface of BA tube to form BA@(BA) x (BN) 1− x core-shell structure is also achieved via a solute exchange process. The precise control over composition and morphology towards organic alloy helices and core-shell microstructures opens a door for understanding the complex co-assembly features of two or more different material partners with similar structures.
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Light-Controlled Self-Assembly of Semiconductor Nanoparticles into Twisted Ribbons
Sudhanshu Srivastava, Aaron Santos, Kevin Critchley et al. · Science · 2010 · 379 citations · Full text