Synthesis and estimation of gelation ability of C3-symmetry tris-urea compounds
-
Add time:08/22/2019 Source:sciencedirect.com
C3-Symmetry tris-urea low molecular weight gelator (LMWG) (1), which shows chemical stimuli responsible for a sol–gel phase transition, was divided into five regions. Based on the division, 22 derivatives were synthesized. The gelation ability of these derivatives was tested in nine organic solvents with a wide range of values for relative static permittivity (ɛr=47.2–1.89). Some derivatives showed a better performance as LMWGs than the original tris-urea LMWG (1). For example, the critical gelation concentration (CGC) in acetone was improved from 1.5 wt % to 0.5 wt % by changing the core substituent (18). Highly versatile LMWG for a variety of solvents was obtained by changing the linker moiety (23). Structural information to design tris-urea LMWGs is important to create rationally a functional supramolecular gel.
We also recommend Trading Suppliers and Manufacturers of (2-ethylphenyl)urea (cas 114-32-9). Pls Click Website Link as below: cas 114-32-9 suppliers
Prev:Novel trifluoromethylpyrazole acyl urea derivatives: Synthesis, crystal structure, fungicidal activity and docking study
Next:Carbamates/Ureas) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Original articlePyridine-3-carboxamide-6-yl-ureas as novel inhibitors of bacterial DNA gyrase: Structure based design, synthesis, SAR and antimicrobial activity08/25/2019
- p38 Kinase inhibitors for the treatment of arthritis and osteoporosis: thienyl, furyl, and pyrrolyl ureas08/24/2019
- Carbamates/Ureas08/23/2019
- Novel trifluoromethylpyrazole acyl urea derivatives: Synthesis, crystal structure, fungicidal activity and docking study08/21/2019


