journal article·2021-07

Thermal and Gas Adsorption Properties of Tröger's Base/Diaza‐cyclooctane Hybrid Ladder Polymers

Keiki Inoue, Roman Selyanchyn, Shigenori Fujikawa, Fumitaka Ishiwari, Takanori Fukushima

ChemNanoMat· Volume 7· Issue 7
Publisher page

Abstract

Abstract A polymer of intrinsic microporosity (PIM) consisting of Tröger's base (TB) undergoes ring opening of the bicyclic amine upon N‐methylation followed by alkaline hydrolysis, resulting in a hybrid ladder polymer that contains diazacyclooctane (DACO) units with tert‐ and sec‐amino groups. The hybrid ladder polymers with various TB/DACO ratios can be prepared depending on the reaction conditions. Here we report a systematic study on the effect of DACO content on the thermal and gas adsorption properties of the hybrid ladder polymer. Using a PIM derived from 2,5‐diamino‐p‐xylene, we prepared hybrid ladder polymers with a DACO content ranging from 19% to 55% while having a similar molecular weight. The thermal stability of the hybrid ladder polymers, evaluated by thermogravimetric analysis, is decreased with the increase in DACO content. Based on gas adsorption measurements, the increase in DACO content results in the decrease in the BET surface area but improves the gas adsorption selectivity for CO2 against N2, likely due to high basicity of the sec‐amino group of DACO unit. This result demonstrates that the partial TB‐to‐DACO conversion of the TB‐based PIM may provide a simple but useful strategy to design polymer materials that enable selective CO2 capture and/or separation.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Covalent Organic Framework Applications · Membrane Separation and Gas Transport · Metal-Organic Frameworks: Synthesis and Applications

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

Affiliations

Laboratory for Chemistry and Life Science, Institute of Innovative Research Tokyo Institute of Technology 4259 Nagatsuta, Midori-ku Yokohama 226-8503 Japan

WPI International Institute for Carbon- Neutral Energy Research (WPI−I2CNER) Kyushu University Fukuoka 819-0395 Japan

Research Center for Negative Emissions Technologies Kyushu University Fukuoka 819-0395 Japan

Center for Molecular Systems (CMS) Kyushu University Fukuoka 819-0395 Japan

Present address: 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 · Japan Prize Foundation · Ministry of Education, Culture, Sports, Science and Technology · Tokyo Institute of Technology

References (55)

Show source-provided references
1.
2. 10.1351/pac19936507156110.1351/pac199365071561 ↗
3. 10.1002/adma.1991003060310.1002/adma.19910030603 ↗
4. 10.1039/a900447e10.1039/a900447e ↗
5. 10.1002/adma.20080058010.1002/adma.200800580 ↗
6. 10.1021/ar300170b10.1021/ar300170b ↗
7. 10.1039/C7SC00154A10.1039/C7SC00154A ↗
8. 10.1002/chem.20170221910.1002/chem.201702219 ↗
9. 10.1039/C5CS00183H10.1039/C5CS00183H ↗
10. 10.1038/368831a010.1038/368831a0 ↗
11.
12. 10.1021/ja00096a05610.1021/ja00096a056 ↗
13. 10.1021/jacs.8b1386510.1021/jacs.8b13865 ↗
14. 10.1038/nchem.181910.1038/nchem.1819 ↗
15. 10.1021/ma200482210.1021/ma2004822 ↗
16. 10.1039/C5SC02385H10.1039/C5SC02385H ↗
17.
18. 10.1039/b311764b10.1039/b311764b ↗
19. 10.1002/chem.20040086010.1002/chem.200400860 ↗
20.
21. 10.1126/science.122803210.1126/science.1228032 ↗
22. N. B. McKeown M. Carta C. M. James POLYMERISATION METHOD 2013 US2013/0267616 A1;
23. 10.1002/adma.20130578310.1002/adma.201305783 ↗
24.
25. 10.1021/acs.chemrev.7b0062910.1021/acs.chemrev.7b00629 ↗
26. 10.1007/s11426-017-9058-x10.1007/s11426-017-9058-x ↗
27. 10.1016/j.polymer.2020.12273610.1016/j.polymer.2020.122736 ↗
28.
29. 10.1039/b802426j10.1039/b802426j ↗
30. 10.1126/science.123044410.1126/science.1230444 ↗
31. 10.1039/C7CS00041C10.1039/C7CS00041C ↗
32.
33. 10.1126/science.aaa807510.1126/science.aaa8075 ↗
34. 10.1039/C8CS00609A10.1039/C8CS00609A ↗
35. 10.1039/C9CS00322C10.1039/C9CS00322C ↗
36. 10.1039/C9CS00827F10.1039/C9CS00827F ↗
37.
38. 10.1021/ja511041510.1021/ja5110415 ↗
39. 10.1021/acsmacrolett.7b0080610.1021/acsmacrolett.7b00806 ↗
40.
41. 10.1021/acsmacrolett.7b0038510.1021/acsmacrolett.7b00385 ↗
42. 10.1039/C9PY01104H10.1039/C9PY01104H ↗
43. 10.1039/D0PY00603C10.1039/D0PY00603C ↗
44. F. Ishiwari S. Miyake K. Inoue K. Hirose T. Fukushima A. Saeki Asian J. Org. Chem.2021 in press DOI:10.1002/ajoc.202100154.10.1002/ajoc.202100154 ↗
45. 10.1016/j.memsci.2019.11776310.1016/j.memsci.2019.117763 ↗
46. By variable temperature NMR analysis the rate constant (kc) and Gibbs’ free energy (ΔG≠) for activation of the ring flipping of model-3are estimated to bekc=400 s−1 ΔG≠=65.8 kJ/mol and at 70 °C in DMSO-d6(Figure S2).
47.
48. 10.1021/acs.jpclett.8b0042210.1021/acs.jpclett.8b00422 ↗
49. 10.1021/acsmacrolett.9b0048210.1021/acsmacrolett.9b00482 ↗
50.
51. 10.1351/pac19855704060310.1351/pac198557040603 ↗
52. 10.1351/pac19946608173910.1351/pac199466081739 ↗
53.
54. 10.1021/ma401869p10.1021/ma401869p ↗
55. 10.1038/nmat298910.1038/nmat2989 ↗