Determining Chiral Configuration of Diamines via Contact Angle Measurements on Enantioselective Alanine-Appended Benzene-Tricarboxamide Gelators
Source abstract
Abstract
Spectroscopic techniques exist that may discern between enantiomers and assess chiral purity. A nonspectroscopic approach that may be directly observed could provide numerous benefits. Using chiral alanine-appended benzene-tricarboxamide gelators, we reveal a methanol gel system that is capable of providing visual discrimination between enantiomers of various diamines. Specifically, gelation is induced by supramolecular nanofiber assembly resulting from interaction between a chiral gelator and a diamine of opposing chirality (i.e., a heterochiral system). Upon further implementing the chiral gelator in electrospun fibers as solid state films, we revealed enantioselective surface wetting properties that allowed for determining chirality through contact angle measurements. While these two approaches of observable gelation and surface wetting offer nonspectroscopic approaches, we also find that the supramolecular nanofiber assembly was able to enhance the induced circular dichroism signal resulting from addition of chiral diamines, allowing precise quantification of their enantiomeric purity.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Supramolecular Self-Assembly in Materials · Chemical Synthesis and Analysis · Lipid Membrane Structure and Behavior
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, Gyeongsang National University, Jinju, 52828, Republic of Korea
Chemical Engineering, Institute of Nano Science and Technology, Hanyang University, 222 Wangsimni-ro, Seoul 133-791, Republic of Korea
Funding
Rural Development Administration · National Research Foundation of Korea
References (45)
Show source-provided references
1. 10.1002/chir.2088910.1002/chir.20889 ↗
2. 10.1021/ja073476s10.1021/ja073476s ↗
3. 10.1039/c3cc43653e10.1039/c3cc43653e ↗
4. 10.1021/ja045978110.1021/ja0459781 ↗
5. 10.1039/B919957H10.1039/B919957H ↗
6. 10.1021/ja803951u10.1021/ja803951u ↗
7. 10.1039/C4CS00104D10.1039/C4CS00104D ↗
8. 10.1039/c3dt50380a10.1039/c3dt50380a ↗
9. 10.1039/b312177c10.1039/b312177c ↗
10. 10.1002/anie.20130044410.1002/anie.201300444 ↗
11. 10.1039/C4MH00078A10.1039/C4MH00078A ↗
12. 10.1002/chem.20140262710.1002/chem.201402627 ↗
13. 10.1039/c2ob26411k10.1039/c2ob26411k ↗
14. 10.1021/cr00007a00910.1021/cr00007a009 ↗
15. 10.1021/ol062711t10.1021/ol062711t ↗
16. 10.1021/ol702843310.1021/ol7028433 ↗
17. 10.1039/b515009d10.1039/b515009d ↗
18. 10.1039/c2ob25613d10.1039/c2ob25613d ↗
19. 10.1021/ja903371d10.1021/ja903371d ↗
20. 10.1021/acs.accounts.5b0000510.1021/acs.accounts.5b00005 ↗
21. 10.1039/C4NJ00417E10.1039/C4NJ00417E ↗
22. 10.1021/ja00408a03310.1021/ja00408a033 ↗
23. 10.1039/c2cc38221k10.1039/c2cc38221k ↗
24. 10.1002/chem.20120340110.1002/chem.201203401 ↗
25. 10.1021/la400562f10.1021/la400562f ↗
26. 10.1002/ange.20118062010.1002/ange.201180620 ↗
27. 10.1021/ja102480t10.1021/ja102480t ↗
28. 10.1038/nmat216710.1038/nmat2167 ↗
29. 10.1021/ja404701s10.1021/ja404701s ↗
30. 10.1002/anie.20130666010.1002/anie.201306660 ↗
31. 10.1021/acsami.5b0798110.1021/acsami.5b07981 ↗
32. 10.1039/C2CC37428E10.1039/C2CC37428E ↗
33. 10.1016/j.gca.2007.03.03910.1016/j.gca.2007.03.039 ↗
34. 10.1002/chem.20100032110.1002/chem.201000321 ↗
35. 10.1002/anie.20150029210.1002/anie.201500292 ↗
36. 10.1002/chem.20120008910.1002/chem.201200089 ↗
37. 10.1021/ja203936910.1021/ja2039369 ↗
38. 10.1021/ja407720510.1021/ja4077205 ↗
39. 10.1021/ja409796b10.1021/ja409796b ↗
40. 10.1039/c3cc45806g10.1039/c3cc45806g ↗
41. 10.1021/la400640710.1021/la4006407 ↗
42. 10.1039/c3nr06752a10.1039/c3nr06752a ↗
43. 10.1016/S0957-4166(03)00586-X10.1016/S0957-4166(03)00586-X ↗
44. Frisch M. J. · 2009
45. 10.1039/c0dt01278e10.1039/c0dt01278e ↗