Donor-acceptor interaction-driven self-assembly of amphiphilic rod-coil molecules into supramolecular nanoassembliesElectronic supplementary information (ESI) available. See DOI: 10.1039/c7nr05329k
Rigid-flexible amphiphilic molecules consisting of an aromatic segment based on pyrene and biphenyl units and hydrophilic polyethylene oxide chains self-assemble into lamellar, hexagonal columnar, and two-dimensional columnar nanostructures in the bulk state. In aqueous solution, these molecules sel...
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Main Authors | , , , , |
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Format | Journal Article |
Language | English |
Published |
23.11.2017
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Online Access | Get full text |
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Summary: | Rigid-flexible amphiphilic molecules consisting of an aromatic segment based on pyrene and biphenyl units and hydrophilic polyethylene oxide chains self-assemble into lamellar, hexagonal columnar, and two-dimensional columnar nanostructures in the bulk state. In aqueous solution, these molecules self-assemble into nanofibers, spherical micelles, and multilayer nanotubes, depending on the chain or rod length of the molecules. Notably, ordered nanostructures of supramolecular polymers, such as single-layer curving fragments, nanofibers, and nanosheets, were constructed through charge-transfer interactions between the nanoobjects and an electron-acceptor molecule, 2,4,5,7-tetranitrofluorenone. These experimental results reveal that diverse supramolecular morphologies can be controlled by tuning rod-coil molecular interactions or charge-transfer interactions between the donor and acceptor molecules.
Pyrene-based amphiphiles self-assemble into nanofibers, spherical micelles and multilayer nanotubes. The addition of TNF allowed polymerization of these objects through charge-transfer interactions to form various supramolecular nanoassemblies. |
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Bibliography: | 10.1039/c7nr05329k Electronic supplementary information (ESI) available. See DOI |
ISSN: | 2040-3364 2040-3372 |
DOI: | 10.1039/c7nr05329k |