journal article·2021-10-13

Facile Preparation of Hierarchically Porous Monolith with Optical Activity Based on Helical Substituted Polyacetylene via One-Step Synthesis for Enantioselective Crystallization

Yan Wang, Luwei Zhang, Taka-Aki Asoh, Hiroshi Uyama

ACS Applied Materials & Interfaces· Volume 13· Issue 40
Publisher page

Abstract

The present study reported the flexible and highly efficient one-step synthesis of chiral hierarchical porous monoliths via cross-linking and polymerization-induced phase separation using substituted acetylene and cross-linker in the presence of porogenic solvent (tetrahydrofuran and methanol) in which the complex doping and complicated procedures were not required. It was demonstrated that hierarchical pore structure with through-pore and high surface area existed in the monoliths, which provides more chiral sites and space for interaction between monolithic materials and the solution. The porous structures and pore size can be adjusted by changing the conditions of phase separation. Moreover, the prepared monoliths exhibited good optical activity, thermal stability and mechanical properties. Therefore, the hierarchically porous monoliths with optical activity were applied in enantioselective crystallization and showed good performance.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Synthesis and Properties of Aromatic Compounds · Covalent Organic Framework Applications · Supramolecular Self-Assembly in Materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Applied Chemistry, Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871, Japan

Funding

Japan Society for the Promotion of Science · China Scholarship Council

References (37)

Show source-provided references
1. 10.1021/cr900162q10.1021/cr900162q ↗
2. 10.1021/acs.chemrev.5b0031710.1021/acs.chemrev.5b00317 ↗
3. 10.1021/cr800555810.1021/cr8005558 ↗
4. 10.1021/cr000097810.1021/cr0000978 ↗
5. 10.1002/chem.20030529510.1002/chem.200305295 ↗
6. 10.1021/acs.chemrev.6b0035410.1021/acs.chemrev.6b00354 ↗
7. 10.1021/acs.macromol.6b0187010.1021/acs.macromol.6b01870 ↗
8. 10.1002/adfm.20090205910.1002/adfm.200902059 ↗
9. 10.1039/C4SC01920B10.1039/C4SC01920B ↗
10. 10.1021/acs.macromol.1c0056310.1021/acs.macromol.1c00563 ↗
11. 10.1016/j.trac.2019.11576210.1016/j.trac.2019.115762 ↗
12. 10.1007/978-3-319-78042-9_110.1007/978-3-319-78042-9_1 ↗
13. 10.1039/D0PY00205D10.1039/D0PY00205D ↗
14. 10.1002/adom.20200085810.1002/adom.202000858 ↗
15. 10.1021/acs.macromol.9b0211810.1021/acs.macromol.9b02118 ↗
16. 10.1039/C2PY20469J10.1039/C2PY20469J ↗
17. 10.1039/C7TC03560H10.1039/C7TC03560H ↗
18. 10.1039/C6CS90043G10.1039/C6CS90043G ↗
19. 10.1016/j.aca.2018.09.06610.1016/j.aca.2018.09.066 ↗
20. 10.1039/C5CS00710K10.1039/C5CS00710K ↗
21. 10.1021/ja00510a07210.1021/ja00510a072 ↗
22. 10.1002/jssc.20110053810.1002/jssc.201100538 ↗
23. 10.1016/j.trac.2015.05.01310.1016/j.trac.2015.05.013 ↗
24. 10.1021/acsami.7b0127510.1021/acsami.7b01275 ↗
25. 10.1016/j.carbpol.2019.03.03610.1016/j.carbpol.2019.03.036 ↗
26. 10.1021/acs.chemmater.6b0126110.1021/acs.chemmater.6b01261 ↗
27. 10.1021/acsmacrolett.5b0061310.1021/acsmacrolett.5b00613 ↗
28. 10.1002/marc.20140054610.1002/marc.201400546 ↗
29. 10.1039/B918132F10.1039/B918132F ↗
30. 10.1021/ma030095010.1021/ma0300950 ↗
31. 10.1002/adfm.20110011310.1002/adfm.201100113 ↗
32. 10.1039/D1MA00185J10.1039/D1MA00185J ↗
33. 10.1111/j.1151-2916.1991.tb06794.x10.1111/j.1151-2916.1991.tb06794.x ↗
34. 10.1038/nature1352710.1038/nature13527 ↗
35. 10.1039/b812587m10.1039/b812587m ↗
36. 10.1007/s10853-016-0702-110.1007/s10853-016-0702-1 ↗
37. 10.1021/acsmacrolett.5b0008810.1021/acsmacrolett.5b00088 ↗