journal article·2026-07-18

Electronic-State Fingerprints of Protonation in Crystalline and Amorphous Molecular Solids

Hironori Suzuki, Yosuke Kimura, Shiori Sakamoto, Namiki Segawa, Masataka Ito, Shuji Noguchi

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Abstract

Resolving protonation-dependent electronic states in molecular solids remains a fundamental challenge, particularly in disordered materials where conventional structural methods fail to provide molecular-level insight. Here, we establish sulfur K-edge X-ray absorption near-edge spectroscopy (XANES) as an atom-specific probe that captures electronic-state fingerprints of protonation and intermolecular interactions in sulfonyl-containing molecular solids. Using glyclopyramide as a representative sulfonylurea compound, crystalline salts, cocrystals, and coamorphous phases were systematically investigated to elucidate how proton transfer modulates local electronic structure. Distinct S K-edge spectral features are highly sensitive to electronic changes in the sulfonylurea moiety, enabling clear discrimination between molecular and ionic states. Notably, these electronic-state fingerprints persist in coamorphous phases, demonstrating that protonation-dependent electronic structures can be resolved even in the absence of long-range order. Correlation of the spectral signatures with supramolecular synthons further reveals a clear relationship between local electronic structure and supramolecular organization across crystalline and amorphous phases. In contrast, Cl K-edge spectra primarily report local chemical environments, highlighting the unique electronic sensitivity of sulfur K-edge analysis. These findings establish electronic-state fingerprints as a robust descriptor of proton-transfer-driven interactions, providing a general framework for understanding and designing crystalline and amorphous molecular materials.s electronic changes in the sulfonylurea moiety, enabling clear discrimination between molecular and ionic states. Notably, these electronic-state fingerprints persist in coamorphous phases, demonstrating that protonation-dependent electronic structures can be resolved even in the absence of long-range order. Correlation of the spectral signatures with supramolecular synthons further reveals a clear relationship between local electronic structure and supramolecular organization across crystalline and amorphous phases. In contrast, Cl K-edge spectra primarily report local chemical environments, highlighting the unique electronic sensitivity of sulfur K-edge analysis. These findings establish electronic-state fingerprints as a robust descriptor of proton-transfer-driven interactions, providing a general framework for understanding and designing crystalline and amorphous molecular materials.
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Research context

OpenAlex topics: Crystallography and molecular interactions · High-pressure geophysics and materials · Spectroscopy and Quantum Chemical Studies

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Affiliations

Faculty of Pharmaceutical Sciences, Toho University, 2-2-1 Miyama, Funabashi, Chiba 274-8514, Japan

Funding

Japan Society for the Promotion of Science

References (45)

Show source-provided references
1. 10.1002/anie.19952311110.1002/anie.199523111 ↗
2. 10.1021/js960189610.1021/js9601896 ↗
3. 10.1016/j.nocx.2023.10018510.1016/j.nocx.2023.100185 ↗
4. 10.1016/S0169-409X(01)00098-910.1016/S0169-409X(01)00098-9 ↗
5. 10.1021/mp060134510.1021/mp0601345 ↗
6. 10.1039/c2ce26055g10.1039/c2ce26055g ↗
7. Giron D. · J. Pharm. Sci. · 2002 · 91 · 210310.1002/jps.10191 ↗
8. Guo J. · Spectrochim. Acta, Part A · 2006 · 65 · 1071
9. 10.1016/j.jpba.2010.05.00210.1016/j.jpba.2010.05.002 ↗
10. 10.1016/0731-7085(93)80083-D10.1016/0731-7085(93)80083-D ↗
11. 10.2138/gsrmg.49.1.110.2138/gsrmg.49.1.1 ↗
12. 10.1039/C9CS00588A10.1039/C9CS00588A ↗
13. 10.1006/jcat.2002.368110.1006/jcat.2002.3681 ↗
14. 10.1111/jace.1433710.1111/jace.14337 ↗
15. 10.1021/acs.inorgchem.5b0193210.1021/acs.inorgchem.5b01932 ↗
16. 10.1016/j.ccr.2004.03.02010.1016/j.ccr.2004.03.020 ↗
17. 10.1021/cr990068110.1021/cr9900681 ↗
18. 10.1007/s11095-021-03151-410.1007/s11095-021-03151-4 ↗
19. 10.1016/j.ijpharm.2023.12272310.1016/j.ijpharm.2023.122723 ↗
20. 10.1248/cpb.c24-0014810.1248/cpb.c24-00148 ↗
21. 10.1021/acs.molpharmaceut.2c0088610.1021/acs.molpharmaceut.2c00886 ↗
22. 10.1248/cpb.c22-0037710.1248/cpb.c22-00377 ↗
23. 10.1021/acs.molpharmaceut.1c0040510.1021/acs.molpharmaceut.1c00405 ↗
24. 10.1016/j.xphs.2020.03.01510.1016/j.xphs.2020.03.015 ↗
25. 10.1016/j.ijpharm.2022.12205710.1016/j.ijpharm.2022.122057 ↗
26. 10.1248/cpb.c23-0039210.1248/cpb.c23-00392 ↗
27. 10.1248/cpb.c21-0091210.1248/cpb.c21-00912 ↗
28. 10.1248/cpb.c25-0022310.1248/cpb.c25-00223 ↗
29. 10.1002/jctb.501002090110.1002/jctb.5010020901 ↗
30. Takashima, Y.; Hosaka, M.; Mano, A.; Yamamoto, N.; Hori, Y.; Takano, T.; Sasaki, S.; Koda, S.; Katoh, M. Proceedings of the 7th International Particle Accelerator Conference (IPAC2016), Busan, Korea. 2016, pp 2877–2879.
31. 10.1088/1742-6596/2380/1/01200110.1088/1742-6596/2380/1/012001 ↗
32. 10.1107/S090904950501271910.1107/S0909049505012719 ↗
33. Ministry of Health, Labour and Welfare. The Japanese Pharmacopoeia 18th ed. 2021.
34. 10.1002/jps.260060090210.1002/jps.2600600902 ↗
35. 10.3390/pharmaceutics603041610.3390/pharmaceutics6030416 ↗
36. 10.1016/j.ejpb.2013.03.01410.1016/j.ejpb.2013.03.014 ↗
37. 10.1007/s13738-021-02425-310.1007/s13738-021-02425-3 ↗
38. 10.1021/ja072182410.1021/ja0721824 ↗
39. 10.1021/acs.cgd.1c0108710.1021/acs.cgd.1c01087 ↗
40. 10.1016/j.gca.2010.07.02210.1016/j.gca.2010.07.022 ↗
41. 10.1039/p298700000s110.1039/p298700000s1 ↗
42. 10.1021/j100785a00110.1021/j100785a001 ↗
43. 10.1107/s090904951002294610.1107/s0909049510022946 ↗
44. 10.1021/acs.chemrev.5b0048410.1021/acs.chemrev.5b00484 ↗
45. 10.1021/cr100072x10.1021/cr100072x ↗