Gallic ester-based phase-selective gelators
Source abstract
Abstract
A series of gallic ester-based derivatives have been prepared, and their properties as organogelators have been evaluated. It was found that some of them exhibit efficient gelation of substituted/unsubstituted aniline. Interestingly, these organogelators could selectively gelate aniline derivatives from an aniline derivatives/water mixture, which can be suitably exploited in water purification. The morphological structures of the xerogels were investigated by SEM and TEM. The probable factors responsible for the self-assembly of this class of gelators have been studied with the help of XRD and FTIR spectroscopy.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Supramolecular Self-Assembly in Materials · Lipid Membrane Structure and Behavior · Polydiacetylene-based materials and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (35)
Show source-provided references
1. Esch · Angew. Chem., Int. Ed. · 2000 · 39 · 226310.1002/1521-3773(20000703)39:13<2263::AID-ANIE2263>3.0.CO;2-V ↗
2. Brunsveld · Chem. Rev. · 2001 · 101 · 407110.1021/cr990125q ↗
3. Bommel · Angew. Chem., Int. Ed. · 2003 · 42 · 98010.1002/anie.200390284 ↗
4. Sangeetha · Chem. Soc. Rev. · 2005 · 34 · 82110.1039/b417081b ↗
5. George · Acc. Chem. Res. · 2006 · 39 · 48910.1021/ar0500923 ↗
6. Wang · Chem. Commun. · 2006 · 149710.1039/b515412j ↗
7. Shen · Chinese J. Org. Chem. · 2009 · 29 · 321
8. Suzuki · Chem. Soc. Rev. · 2009 · 38 · 96710.1039/b816192e ↗
9. Amabilino · Soft Matter · 2010 · 6 · 160510.1039/b923618j ↗
10. Bhattacharya · Chem. Commun. · 2001 · 18510.1039/b007848o ↗
11. Kiyonaka · J. Am. Chem. Soc. · 2002 · 124 · 1095410.1021/ja027277e ↗
12. Vintiloiu · J. Controlled Release · 2008 · 125 · 17910.1016/j.jconrel.2007.09.014 ↗
13. Kobayashi · J. Am. Chem. Soc. · 2002 · 124 · 655010.1021/ja0260622 ↗
14. Llusar · Chem. Mater. · 2008 · 20 · 78210.1021/cm702141e ↗
15. Dastidar · Chem. Soc. Rev. · 2008 · 37 · 269910.1039/b807346e ↗
16. Esch · Langmuir · 2009 · 25 · 839210.1021/la901720a ↗
17. Trivedi · Chem. Mater. · 2003 · 15 · 397110.1021/cm034288d ↗
18. Trivedi · Chem.–Eur. J. · 2004 · 10 · 531110.1002/chem.200400122 ↗
19. Debnath · Chem.–Eur. J. · 2008 · 14 · 687010.1002/chem.200800731 ↗
20. Xue · Tetrahedron · 2009 · 65 · 336910.1016/j.tet.2009.02.056 ↗
21. Jadhav · Angew. Chem., Int. Ed. · 2010 · 49 · 769510.1002/anie.201002095 ↗
22. Seo · Angew. Chem., Int. Ed. · 2006 · 45 · 752610.1002/anie.200600688 ↗
23. Hirst · J. Am. Chem. Soc. · 2008 · 130 · 911310.1021/ja801804c ↗
24. Wu · Chem.–Eur. J. · 2009 · 15 · 623410.1002/chem.200900409 ↗
25. Menger · Angew. Chem., Int. Ed. · 2000 · 39 · 190610.1002/1521-3773(20000602)39:11<1906::AID-ANIE1906>3.0.CO;2-Q ↗
26. Menger · J. Am. Chem. Soc. · 2003 · 125 · 534010.1021/ja021298r ↗
27. Uzun · J. Am. Chem. Soc. · 2004 · 126 · 1477310.1021/ja047643p ↗
28. Hu · J. Am. Chem. Soc. · 2005 · 127 · 652610.1021/ja050053m ↗
29. Akutagawa · Angew. Chem., Int. Ed. · 2005 · 44 · 728310.1002/anie.200502336 ↗
30. Kim · Chem. Commun. · 2005 · 203510.1039/B419258C ↗
31. Kumar · Angew. Chem., Int. Ed. · 2006 · 45 · 631710.1002/anie.200602088 ↗
32. Tung · J. Am. Chem. Soc. · 2008 · 130 · 881310.1021/ja801895n ↗
33. Peng · Langmuir · 2008 · 24 · 299210.1021/la703672u ↗
34. Masuda · J. Am. Chem. Soc. · 2000 · 122 · 1232710.1021/ja001884p ↗
35. Würthner · Chem. Eur. J. · 2001 · 7 · 224510.1002/1521-3765(20010518)7:10<2245::AID-CHEM2245>3.0.CO;2-W ↗