journal article·2026-05Open access

Can Entropically Unfavorable Topological Hydrogen‐Bonded Networks Form From Tetrakis‐ or Pentakis(4‐Carboxyphenyl)benzene Derivative?

Rento Maeda, Ryusei Oketani, Kazuki Shiga, Norimitsu Tohnai, Ichiro Hisaki

Small· Volume 22· Issue 28

Abstract

ABSTRACT Control of network topology is one of the most important issues in reticular chemistry. Herein, we report the network structures of the missing pieces of carboxyphenylbenzene (CPB) derivatives, the simplest series of building blocks for hydrogen‐bonded organic frameworks (HOFs), and elucidate their network topology in a crystalline state. 1,2,3,5‐Tetrakis‐ and 1,2,3,4,5‐pentakisCPBs ( 1235CPB and 12345CPB ) form H‐bonded networks with sql ‐ and cem ‐topologies, respectively. Furthermore, it is remarkable that 1235CPB forms a more complicated cqe ‐topological network structure with three kinds of voids in crystalline states under the same crystallization condition, although the formation occurs infrequently. The network structure with cqe ‐topology is hitherto unknown in molecule‐based framework materials. Other molecules in the series of CPB gave no H‐bonded network with complicated topology, enabling us to estimate the limitation for generating entropically unfavorable networks on the basis of a simple consideration of the number of cases for the network formation. We also report thermal behaviors, porosity, and structural transformation of these H‐bonded network crystals from a materials perspective.
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Research context

OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Supramolecular Self-Assembly in Materials · Covalent Organic Framework Applications

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

Affiliations

Division of Chemistry Graduate School of Engineering Science The University of Osaka Toyonaka Osaka Japan

Division of Applied Chemistry Graduate School of Engineering The University of Osaka Suita Osaka Japan

Funding

Japan Society for the Promotion of Science

References (56)

Show source-provided references
1. 10.1039/C9CS00893D10.1039/C9CS00893D ↗
2. 10.1039/c3ce40929e10.1039/c3ce40929e ↗
3. 10.1016/j.chempr.2021.07.00610.1016/j.chempr.2021.07.006 ↗
4. 10.1021/cr200205j10.1021/cr200205j ↗
5. 10.1021/acs.chemrev.0c0104910.1021/acs.chemrev.0c01049 ↗
6. 10.1002/sstr.20210021010.1002/sstr.202100210 ↗
7. 10.1016/j.giant.2023.10017010.1016/j.giant.2023.100170 ↗
8. 10.1021/jacs.4c1445810.1021/jacs.4c14458 ↗
9. 10.1021/ar800124u10.1021/ar800124u ↗
10. 10.1021/cr400392k10.1021/cr400392k ↗
11. 10.1021/cg500498k10.1021/cg500498k ↗
12. 10.1021/cr500150m10.1021/cr500150m ↗
13. 10.1038/s43246‐024‐00690‐210.1038/s43246‐024‐00690‐2 ↗
14. 10.1039/C6SC05673C10.1039/C6SC05673C ↗
15. 10.1021/jacs.3c0172910.1021/jacs.3c01729 ↗
16. 10.1039/C8CS00155C10.1039/C8CS00155C ↗
17. 10.1002/ange.20190214710.1002/ange.201902147 ↗
18. 10.1021/jacs.0c0647310.1021/jacs.0c06473 ↗
19. 10.1021/jacs.2c0259810.1021/jacs.2c02598 ↗
20. 10.1021/accountsmr.0c0001910.1021/accountsmr.0c00019 ↗
21. 10.1016/j.jphotochemrev.2021.10041810.1016/j.jphotochemrev.2021.100418 ↗
22. 10.1002/advs.20240010110.1002/advs.202400101 ↗
23. 10.1002/adfm.20240363510.1002/adfm.202403635 ↗
24. 10.1039/C5CC04219D10.1039/C5CC04219D ↗
25. 10.1021/acsnano.7b0444710.1021/acsnano.7b04447 ↗
26. 10.1039/D4CC06324D10.1039/D4CC06324D ↗
27. 10.1002/anie.20181126310.1002/anie.201811263 ↗
28. 10.1002/anie.20170811510.1002/anie.201708115 ↗
29. 10.1039/D4SC01218F10.1039/D4SC01218F ↗
30. 10.1021/ja067571x10.1021/ja067571x ↗
31. 10.1007/s10847‐019‐00972‐010.1007/s10847‐019‐00972‐0 ↗
32. 10.1038/s41428‐023‐00840‐210.1038/s41428‐023‐00840‐2 ↗
33. 10.1016/S0040‐4039(99)02008‐010.1016/S0040‐4039(99)02008‐0 ↗
34. 10.1021/acs.cgd.4c0169710.1021/acs.cgd.4c01697 ↗
35. 10.1093/chemle/upaf11110.1093/chemle/upaf111 ↗
36. 10.1002/anie.20141143810.1002/anie.201411438 ↗
37. 10.1039/C7CE00183E10.1039/C7CE00183E ↗
38. 10.1021/jacs.2c0108210.1021/jacs.2c01082 ↗
39. 10.1021/acsami.9b0369610.1021/acsami.9b03696 ↗
40. 10.1002/anie.20180035410.1002/anie.201800354 ↗
41. 10.1021/jo01301a00410.1021/jo01301a004 ↗
42. 10.1002/chem.20140209210.1002/chem.201402092 ↗
43. 10.1021/ar00052a00510.1021/ar00052a005 ↗
44. 10.1002/anie.20141035610.1002/anie.201410356 ↗
45. 10.1021/jacs.6b0296810.1021/jacs.6b02968 ↗
46. 10.1002/chem.20170189310.1002/chem.201701893 ↗
47. 10.1002/anie.20180547210.1002/anie.201805472 ↗
48. 10.1021/cg901074610.1021/cg9010746 ↗
49. 10.1107/S205322961402492910.1107/S2053229614024929 ↗
50. 10.1002/anie.20161090110.1002/anie.201610901 ↗
51. 10.1039/C8TA02211A10.1039/C8TA02211A ↗
52. 10.1039/D1SC02690A10.1039/D1SC02690A ↗
53. 10.1039/D1CC03287A10.1039/D1CC03287A ↗
54. 10.1002/chem.20240164510.1002/chem.202401645 ↗
55. 10.1002/anie.20251097710.1002/anie.202510977 ↗
56. 10.1002/chem.20250230310.1002/chem.202502303 ↗