Effects of Hydrogen Bonding and van der Waals Interactions on Organogelation Using Designed Low-Molecular-Weight Gelators and Gel Formation at Room Temperature
We synthesized novel l-lysine-based compounds that were classified into three groups, urea−urea types (1−3), amide−urea types (4−6), and amide−amide type (7), and examined the effects of hydrogen bonding and van der Waals interactions on the organogelation behavior. Among these compounds, gelator 5...
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Published in | Langmuir Vol. 19; no. 21; pp. 8622 - 8624 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
American Chemical Society
14.10.2003
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Online Access | Get full text |
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Summary: | We synthesized novel l-lysine-based compounds that were classified into three groups, urea−urea types (1−3), amide−urea types (4−6), and amide−amide type (7), and examined the effects of hydrogen bonding and van der Waals interactions on the organogelation behavior. Among these compounds, gelator 5 has the best organogelation ability. Moreover, the organogelation can be achieved at room temperature through the direct synthesis of gelators in organic solvents. |
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Bibliography: | ark:/67375/TPS-DPM8CV69-H istex:AE91EB102B1D00F4FBA0A15776DCC849777281BC |
ISSN: | 0743-7463 1520-5827 |
DOI: | 10.1021/la034772v |