Chiral Self-Assembly of Designed Amphiphiles: Optimization for Nanotube Formation
Four amphiphiles with l-aspartic acid headgroups (Asp) and a diphenyldiazenyl group (Azo) contained within the hydrophobic tails were designed and synthesized for self-assembly into helically based nanotubes. The amphiphiles of the form R′-{4-[(4-alkylphenyl)diazenyl]phenoxy}alkanoyl-l-aspartic acid...
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Published in | Langmuir Vol. 28; no. 40; pp. 14172 - 14179 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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American Chemical Society
09.10.2012
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Abstract | Four amphiphiles with l-aspartic acid headgroups (Asp) and a diphenyldiazenyl group (Azo) contained within the hydrophobic tails were designed and synthesized for self-assembly into helically based nanotubes. The amphiphiles of the form R′-{4-[(4-alkylphenyl)diazenyl]phenoxy}alkanoyl-l-aspartic acid (where R′ is 10 or 11) varied only in alkyl chain lengths either side of the azo group, having 4, 7, or 10 carbon distal chains and 10 or 11 carbon proximal chains (R-Azo-R′-Asp, where R denotes the number of carbons in the distal chain and R′ denotes the number of carbons in the proximal chain). Despite the molecular similarities, distinct differences were identified in the chiral order of the structures self-assembled from hot methanolic aqueous solutions using microscopy and spectroscopic analyses. This was reflected in dominant thermodynamic aggregate morphologies that ranged from amorphous material for 10-Azo-10-Asp, through twisted ribbons (196 ± 49 nm pitch) for 7-Azo-11-Asp, to the desired helically based nanotubes for 4- and 7-Azo-10-Asp (81 ± 11 and 76 ± 6 nm diameters, respectively). Another key variable in the self-assembly of the amphiphiles was the use of a second method to precipitate aggregates from solution at room temperature. This method enabled the isolation of thermodynamically unstable and key transitional structures. Helical ribbons were precursor structures to the nanotubes formed from 4- and 7-Azo-10-Asp as well as the wide, flattened nanotube structures (587 ± 85 nm width) found for 4-Azo-10-Asp. Overall, the results highlighted the interplay of influence of the headgroup and the hydrophobic tail on self-assembly, providing a basis for future rational design of self-assembling amphiphiles. |
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AbstractList | Four amphiphiles with L-aspartic acid headgroups (Asp) and a diphenyldiazenyl group (Azo) contained within the hydrophobic tails were designed and synthesized for self-assembly into helically based nanotubes. The amphiphiles of the form R'-{4-[(4-alkylphenyl)diazenyl]phenoxy}alkanoyl-L-aspartic acid (where R' is 10 or 11) varied only in alkyl chain lengths either side of the azo group, having 4, 7, or 10 carbon distal chains and 10 or 11 carbon proximal chains (R-Azo-R'-Asp, where R denotes the number of carbons in the distal chain and R' denotes the number of carbons in the proximal chain). Despite the molecular similarities, distinct differences were identified in the chiral order of the structures self-assembled from hot methanolic aqueous solutions using microscopy and spectroscopic analyses. This was reflected in dominant thermodynamic aggregate morphologies that ranged from amorphous material for 10-Azo-10-Asp, through twisted ribbons (196 ± 49 nm pitch) for 7-Azo-11-Asp, to the desired helically based nanotubes for 4- and 7-Azo-10-Asp (81 ± 11 and 76 ± 6 nm diameters, respectively). Another key variable in the self-assembly of the amphiphiles was the use of a second method to precipitate aggregates from solution at room temperature. This method enabled the isolation of thermodynamically unstable and key transitional structures. Helical ribbons were precursor structures to the nanotubes formed from 4- and 7-Azo-10-Asp as well as the wide, flattened nanotube structures (587 ± 85 nm width) found for 4-Azo-10-Asp. Overall, the results highlighted the interplay of influence of the headgroup and the hydrophobic tail on self-assembly, providing a basis for future rational design of self-assembling amphiphiles. |
Author | Constantopoulos, Kristina Fujiki, Michiya Barclay, Thomas G Matisons, Janis G Zhang, Wei |
AuthorAffiliation | Flinders University Nara Institute of Science and Technology |
AuthorAffiliation_xml | – name: Flinders University – name: Nara Institute of Science and Technology |
Author_xml | – sequence: 1 givenname: Thomas G surname: Barclay fullname: Barclay, Thomas G email: thomas.barclay@flinders.edu.au – sequence: 2 givenname: Kristina surname: Constantopoulos fullname: Constantopoulos, Kristina – sequence: 3 givenname: Wei surname: Zhang fullname: Zhang, Wei – sequence: 4 givenname: Michiya surname: Fujiki fullname: Fujiki, Michiya – sequence: 5 givenname: Janis G surname: Matisons fullname: Matisons, Janis G |
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Keywords | Self assembly Amorphous material Similarity Chain length Nanotube Hydrophobicity Precipitate Carbon Precursor Optimization Design Thermodynamics Alkyl Morphology Pitch Aspartic acid Aqueous solution Aggregate Structure Diameter Room temperature |
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Snippet | Four amphiphiles with l-aspartic acid headgroups (Asp) and a diphenyldiazenyl group (Azo) contained within the hydrophobic tails were designed and synthesized... Four amphiphiles with L-aspartic acid headgroups (Asp) and a diphenyldiazenyl group (Azo) contained within the hydrophobic tails were designed and synthesized... |
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Title | Chiral Self-Assembly of Designed Amphiphiles: Optimization for Nanotube Formation |
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