Dipeptide-based low-molecular-weight efficient organogelators and their application in water purification
- PMID: 18642259
- DOI: 10.1002/chem.200800731
Dipeptide-based low-molecular-weight efficient organogelators and their application in water purification
Abstract
The development of new low-molecular-weight gelators for organic solvents is motivated by several potential applications of gels as advanced functional materials. In the present study, we developed simple dipeptide-based organogelators with a minimum gelation concentration (MGC) of 6-0.15 %, w/v in aromatic solvents. The organogelators were synthesized using different L-amino acids with nonpolar aliphatic/aromatic residues and by varying alkyl-chain length (C-12 to C-16). The self-aggregation behavior of these thermoreversible organogels was investigated through several spectroscopic and microscopic techniques. A balanced participation of the hydrogen bonding and van der Waals interactions is crucial for efficient organogelation, which can be largely modulated by the structural modification at the hydrogen-bonding unit as well as by varying the alkyl-chain length in both sides of the hydrophilic residue. Interestingly, these organogelators could selectively gelate aromatic solvents from their mixtures with water. Furthermore, the xerogels prepared from the organogels showed a striking property of adsorbing dyes such as crystal violet, rhodamine 6G from water. This dye-adsorption ability of gelators can be utilized in water purification by removing toxic dyes from wastewater.
Similar articles
-
Organogelation and hydrogelation of low-molecular-weight amphiphilic dipeptides: pH responsiveness in phase-selective gelation and dye removal.Langmuir. 2009 Aug 4;25(15):8639-48. doi: 10.1021/la804235e. Langmuir. 2009. PMID: 19338331
-
Choice of the end functional groups in tri(p-phenylenevinylene) derivatives controls its physical gelation abilities.Langmuir. 2009 Aug 4;25(15):8567-78. doi: 10.1021/la8036154. Langmuir. 2009. PMID: 19402602
-
Structure and properties of low molecular weight amphiphilic peptide hydrogelators.J Phys Chem B. 2007 Dec 27;111(51):14107-13. doi: 10.1021/jp076495x. Epub 2007 Dec 4. J Phys Chem B. 2007. PMID: 18052148
-
Organogels and their use in drug delivery--a review.J Control Release. 2008 Feb 11;125(3):179-92. doi: 10.1016/j.jconrel.2007.09.014. Epub 2007 Nov 7. J Control Release. 2008. PMID: 18082283 Review.
-
Organogels in drug delivery.Expert Opin Drug Deliv. 2005 May;2(3):489-505. doi: 10.1517/17425247.2.3.489. Expert Opin Drug Deliv. 2005. PMID: 16296770 Review.
Cited by
-
Self-assembly and multifunctionality of peptide organogels: oil spill recovery, dye absorption and synthesis of conducting biomaterials.RSC Adv. 2020 Jan 31;10(9):5220-5233. doi: 10.1039/c9ra10395c. eCollection 2020 Jan 29. RSC Adv. 2020. PMID: 35498311 Free PMC article.
-
Gelation behavior of short protected peptides in organic medium.Soft Matter. 2025 Jun 11;21(23):4751-4760. doi: 10.1039/d5sm00275c. Soft Matter. 2025. PMID: 40407806 Free PMC article.
-
Cyclohexamer [-(d-Phe-azaPhe-Ala)2-]: good candidate to formulate supramolecular organogels.RSC Adv. 2020 Dec 7;10(71):43859-43869. doi: 10.1039/d0ra07775e. eCollection 2020 Nov 27. RSC Adv. 2020. PMID: 35519698 Free PMC article.
-
Smart Materials for Environmental Remediation Based on Two-Component Gels: Room-Temperature-Phase-Selective Gelation for the Removal of Organic Pollutants Including Nitrobenzene/O-Dichlorobenzene, and Dye Molecules from the Wastewater.Nanoscale Res Lett. 2019 Feb 1;14(1):42. doi: 10.1186/s11671-019-2865-6. Nanoscale Res Lett. 2019. PMID: 30707315 Free PMC article.
-
Gelatinizing oil in water and its removal via bacteria inhabiting the gels.Sci Rep. 2017 Oct 25;7(1):13975. doi: 10.1038/s41598-017-14296-x. Sci Rep. 2017. PMID: 29070801 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources