Design, Structure, and Applications of 1-Dodecyl-3-(tolyl) Urea Low Molecular Weight Organogelators

This article describes the discovery, characterization and application of a small family of urea-based low molecular weight organogelators (LMWOs), namely the para-, meta- and ortho-1-dodecyl-3-(tolyl) ureas. All three LMWOs were tested for their ability to gel both polar and non-polar solvents and their properties were compared, with 1-dodecyl-3-(o-tolyl) urea proving the most versatile. 1-dodecyl-3-(o-tolyl) urea successfully gelled 1-octadecene, dimethylsulfoxide, petroleum ether, cyclohexane and toluene, with the latter gelling at just 0.8 wt.% of LMWO, making it a supergelator. The ability to gel both polar and non-polar solvents is an interesting and unusual property exhibited by few LMWO molecules, and as such, the applications for this molecule move beyond typical applications such as oil-spill remediation, into the biomedical and cosmetics sphere. Gels were characterized using rheology, small-angle neutron scattering (SANS), scanning electron microscopy (SEM) and differential scanning calorimetry (DSC). Applications of 1-dodecyl-3-(o-tolyl) urea gels of dimethyl sulfoxide demonstrated in this study include in vitro release into an aqueous medium and bioimaging agent delivery.

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Publication Details

Journal
Gels
Published
2026-11-04
DOI
https://doi.org/10.3390/gels12111005
Primary Topic
Supramolecular Self-Assembly in Materials
Type
article
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article

Design, Structure, and Applications of 1-Dodecyl-3-(tolyl) Urea Low Molecular Weight Organogelators

William J. Peveler, Joseph C. Bear, Peter Stephen Patrick, Wafaa Al-Shatty et al.
Gels
Supramolecular Self-Assembly in Materials
article

Design, Structure, and Applications of 1-Dodecyl-3-(tolyl) Urea Low Molecular Weight Organogelators

William J. Peveler, Joseph C. Bear, Peter Stephen Patrick, Wafaa Al-Shatty, Shirin Alexander, Sarah E. Rogers, Hollie Packman, Cecile Ayako Dreiss, Jeremy K. Cockcroft
article en

Abstract

This article describes the discovery, characterization and application of a small family of urea-based low molecular weight organogelators (LMWOs), namely the para-, meta- and ortho-1-dodecyl-3-(tolyl) ureas. All three LMWOs were tested for their ability to gel both polar and non-polar solvents and their properties were compared, with 1-dodecyl-3-(o-tolyl) urea proving the most versatile. 1-dodecyl-3-(o-tolyl) urea successfully gelled 1-octadecene, dimethylsulfoxide, petroleum ether, cyclohexane and toluene, with the latter gelling at just 0.8 wt.% of LMWO, making it a supergelator. The ability to gel both polar and non-polar solvents is an interesting and unusual property exhibited by few LMWO molecules, and as such, the applications for this molecule move beyond typical applications such as oil-spill remediation, into the biomedical and cosmetics sphere. Gels were characterized using rheology, small-angle neutron scattering (SANS), scanning electron microscopy (SEM) and differential scanning calorimetry (DSC). Applications of 1-dodecyl-3-(o-tolyl) urea gels of dimethyl sulfoxide demonstrated in this study include in vitro release into an aqueous medium and bioimaging agent delivery.

GelsVol. 12(11)
Rutherford Appleton Laboratory (GB), King's College London (GB), Kingston University London (GB), Swansea University (GB), University College London (GB), Imperial College London (GB), University of Glasgow (GB)
Openalex Percentile: Top 30%
Supramolecular Self-Assembly in Materials
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