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 inLangmuir Vol. 28; no. 40; pp. 14172 - 14179
Main Authors Barclay, Thomas G, Constantopoulos, Kristina, Zhang, Wei, Fujiki, Michiya, Matisons, Janis G
Format Journal Article
LanguageEnglish
Published Washington, DC 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.
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
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Issue 40
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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SubjectTerms Chemistry
Exact sciences and technology
General and physical chemistry
Title Chiral Self-Assembly of Designed Amphiphiles: Optimization for Nanotube Formation
URI http://dx.doi.org/10.1021/la3030606
https://www.ncbi.nlm.nih.gov/pubmed/22973868
https://search.proquest.com/docview/1095633765
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