Self-Assembly of Alkylamido Isophthalic Acids toward the Design of a Supergelator: Phase-Selective Gelation and Dye Adsorption

A new series of 5-alkylamido isophthalic acid (ISA) derivatives with varying single and twin alkyl chain lengths were designed and synthesized as potential supramolecular organogelators. 5-alkylamido ISAs with linear or branched alkyl tail-groups of different lengths were effective gelators for low...

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Main Authors: Darren A. Makeiff, Jae-Young Cho, Bradley Smith, Rina Carlini, Nicolas Godbert
Format: Article
Language:English
Published: MDPI AG 2022-05-01
Series:Gels
Subjects:
Online Access:https://www.mdpi.com/2310-2861/8/5/285
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author Darren A. Makeiff
Jae-Young Cho
Bradley Smith
Rina Carlini
Nicolas Godbert
author_facet Darren A. Makeiff
Jae-Young Cho
Bradley Smith
Rina Carlini
Nicolas Godbert
author_sort Darren A. Makeiff
collection DOAJ
description A new series of 5-alkylamido isophthalic acid (ISA) derivatives with varying single and twin alkyl chain lengths were designed and synthesized as potential supramolecular organogelators. 5-alkylamido ISAs with linear or branched alkyl tail-groups of different lengths were effective gelators for low polarity solvents. In particular, among the presented series, a derivative with a branched, 24 carbon atom tail-group behaves as a “supergelator” with up to twenty organic solvents forming gels that are highly stable over time. The gelation behavior was analyzed using Hansen solubility parameters, and the thermal stability and viscoelastic properties of select gels were characterized. Microscopy, spectroscopy, powder X-ray diffraction, and computer modeling studies were consistent with a hierarchical self-assembly process involving the formation of cyclic H-bonded hexamers via the ISA carboxylic acid groups, which stack into elementary fibers stabilized by H-bonding of the amide linker groups and π–π stacking of the aromatic groups. These new nanomaterials exhibited potential for the phase-selective gelation of oil from oil–water mixtures and dye uptake from contaminated water. The work expands upon the design and synthesis of supramolecular self-assembled nanomaterials and their application in water purification/remediation.
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spelling doaj.art-8351a8a7c20e47869608f31427c897ff2023-11-23T11:05:07ZengMDPI AGGels2310-28612022-05-018528510.3390/gels8050285Self-Assembly of Alkylamido Isophthalic Acids toward the Design of a Supergelator: Phase-Selective Gelation and Dye AdsorptionDarren A. Makeiff0Jae-Young Cho1Bradley Smith2Rina Carlini3Nicolas Godbert4Nanotechnology Research Center, National Research Council of Canada, 11421 Saskatchewan Drive, Edmonton, AB T6G 2M9, CanadaNanotechnology Research Center, National Research Council of Canada, 11421 Saskatchewan Drive, Edmonton, AB T6G 2M9, CanadaNanotechnology Research Center, National Research Council of Canada, 11421 Saskatchewan Drive, Edmonton, AB T6G 2M9, CanadaOptimal Innovation Group Inc., 175 Longwood Rd. S, Suite 112 A, Hamilton, ON L8P 0A1, CanadaDipartimento di Chimica e Tecnologie Chimiche, Università della Calabria, 87036 Rende, ItalyA new series of 5-alkylamido isophthalic acid (ISA) derivatives with varying single and twin alkyl chain lengths were designed and synthesized as potential supramolecular organogelators. 5-alkylamido ISAs with linear or branched alkyl tail-groups of different lengths were effective gelators for low polarity solvents. In particular, among the presented series, a derivative with a branched, 24 carbon atom tail-group behaves as a “supergelator” with up to twenty organic solvents forming gels that are highly stable over time. The gelation behavior was analyzed using Hansen solubility parameters, and the thermal stability and viscoelastic properties of select gels were characterized. Microscopy, spectroscopy, powder X-ray diffraction, and computer modeling studies were consistent with a hierarchical self-assembly process involving the formation of cyclic H-bonded hexamers via the ISA carboxylic acid groups, which stack into elementary fibers stabilized by H-bonding of the amide linker groups and π–π stacking of the aromatic groups. These new nanomaterials exhibited potential for the phase-selective gelation of oil from oil–water mixtures and dye uptake from contaminated water. The work expands upon the design and synthesis of supramolecular self-assembled nanomaterials and their application in water purification/remediation.https://www.mdpi.com/2310-2861/8/5/285supramolecular organogelself-assemblyisophthalic acidHansen solubility parametersrheologyphase-selective gelation
spellingShingle Darren A. Makeiff
Jae-Young Cho
Bradley Smith
Rina Carlini
Nicolas Godbert
Self-Assembly of Alkylamido Isophthalic Acids toward the Design of a Supergelator: Phase-Selective Gelation and Dye Adsorption
Gels
supramolecular organogel
self-assembly
isophthalic acid
Hansen solubility parameters
rheology
phase-selective gelation
title Self-Assembly of Alkylamido Isophthalic Acids toward the Design of a Supergelator: Phase-Selective Gelation and Dye Adsorption
title_full Self-Assembly of Alkylamido Isophthalic Acids toward the Design of a Supergelator: Phase-Selective Gelation and Dye Adsorption
title_fullStr Self-Assembly of Alkylamido Isophthalic Acids toward the Design of a Supergelator: Phase-Selective Gelation and Dye Adsorption
title_full_unstemmed Self-Assembly of Alkylamido Isophthalic Acids toward the Design of a Supergelator: Phase-Selective Gelation and Dye Adsorption
title_short Self-Assembly of Alkylamido Isophthalic Acids toward the Design of a Supergelator: Phase-Selective Gelation and Dye Adsorption
title_sort self assembly of alkylamido isophthalic acids toward the design of a supergelator phase selective gelation and dye adsorption
topic supramolecular organogel
self-assembly
isophthalic acid
Hansen solubility parameters
rheology
phase-selective gelation
url https://www.mdpi.com/2310-2861/8/5/285
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