journal article·2026-05-12

Systematic Synthesis of Lead–Benzenethiolate Coordination Polymers: Influence of Halogen Substituents on Crystal Structure and Semiconducting Properties

Miyu Inoue, Ryohei Akiyoshi, Akinori Saeki, Naohiro Takahashi, Takashi Okubo, Daisuke Kosumi, Yasutaka Kitagawa, Yuiga Nakamura, Yuki Mori, Shogo Kawaguchi, Kazuyoshi Ogasawara, Daisuke Tanaka

Chemistry of Materials· Volume 38· Issue 9
Publisher page

Abstract

Coordination polymers containing sulfur coordination atoms (S-CPs) represent an emerging class of organic–inorganic hybrid semiconductors. Notably, Pb(II)-based S-CPs have garnered increasing attention due to their high electron mobility and narrow band gaps, rendering them promising materials for use in a wide-range optoelectronic applications. Although the semiconducting properties of Pb(II) S-CPs are significantly influenced by the local coordination environment and the (–Pb–S–)n dimensionality, rational design strategies for precisely tuning their crystal structure remain limited. In this study, Pb(II) S-CPs are systematically synthesized using halogen-substituted benzenethiol ligands (HSPhX = 4-halobenzenethiol; X = F, Cl, Br, I), giving the general formula [Pb(SPhX)2]. Single-crystal X-ray diffraction and density functional theory calculations suggest that the electron-withdrawing ability of the halogen substituents modulates the electron density on the thiolate S atoms, thereby governing the S-coordination mode and dimensionality of the (–Pb–S–)n network. Among the synthesized series, KGF-70(I), which was obtained using the weakly electron-withdrawing HSPhI, forms a holodirected coordination geometry and a two-dimensionally-extended (–Pb–S–)n network, resulting in enhanced charge carrier mobility, narrow band gap energy, and anomalous band structure. Furthermore, the potential applicability of KGF-70(I) as a photodetector is demonstrated. Overall, this systematic investigation offers a rational design strategy for tailoring the crystal structure and semiconducting properties of Pb(II) S-CPs.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Organic and Molecular Conductors Research · Organometallic Compounds Synthesis and Characterization

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

Affiliations

School of Science, Kwansei Gakuin University, 1 Gakuen Uegahara, Sanda, Hyogo 669-1330, Japan

Graduate School of Engineering, The University of Osaka, 2-1 Yamadaoka, Suita, Osaka 565-0871, Japan

Faculty of Science and Engineering

Kindai University

Institute of Industrial Nanomaterials, Kumamoto University, 2-39-1 Kurokami, Chuo-ku, Kumamoto 860-8555, Japan

Graduate School of Engineering Science

The University of Osaka

Japan Synchrotron Radiation Research Institute

Funding

Toyota Physical and Chemical Research Institute · Tokuyama Science Foundation · Japan Society for the Promotion of Science · Kawanishi Memorial ShinMaywa Education Foundation

References (56)

Show source-provided references
1. 10.1002/cptc.20170014510.1002/cptc.201700145 ↗
2. 10.1039/D0SC03429K10.1039/D0SC03429K ↗
3. 10.1039/D0CS01393E10.1039/D0CS01393E ↗
4. 10.1246/cl.20077710.1246/cl.200777 ↗
5. 10.1016/j.ccr.2021.21423510.1016/j.ccr.2021.214235 ↗
6. 10.1002/anie.20220315110.1002/anie.202203151 ↗
7. 10.1039/D3DT02884D10.1039/D3DT02884D ↗
8. 10.1021/acsnano.4c1849310.1021/acsnano.4c18493 ↗
9. 10.1021/ja403751610.1021/ja4037516 ↗
10. 10.1021/jacs.5b0289710.1021/jacs.5b02897 ↗
11. 10.1039/C8DT02197J10.1039/C8DT02197J ↗
12. 10.1016/j.cocr.2025.10001310.1016/j.cocr.2025.100013 ↗
13. 10.1039/C5CC10448C10.1039/C5CC10448C ↗
14. 10.1039/C5TC00119F10.1039/C5TC00119F ↗
15. 10.3390/nano910140810.3390/nano9101408 ↗
16. 10.1039/D3TC04362B10.1039/D3TC04362B ↗
17. 10.1002/chem.20070072310.1002/chem.200700723 ↗
18. 10.1038/nmat482310.1038/nmat4823 ↗
19. 10.1021/jacs.8b0792110.1021/jacs.8b07921 ↗
20. 10.1016/j.ccr.2017.08.01410.1016/j.ccr.2017.08.014 ↗
21. 10.1038/s41467-019-09682-010.1038/s41467-019-09682-0 ↗
22. 10.1021/acs.inorgchem.8b0125710.1021/acs.inorgchem.8b01257 ↗
23. 10.1038/s41467-019-14136-810.1038/s41467-019-14136-8 ↗
24. 10.1002/anie.20211062910.1002/anie.202110629 ↗
25. 10.1016/j.ccr.2020.21371710.1016/j.ccr.2020.213717 ↗
26. 10.1039/D2CC02114E10.1039/D2CC02114E ↗
27. 10.1038/s41467-025-56609-z10.1038/s41467-025-56609-z ↗
28. 10.1039/d4cc06171c10.1039/d4cc06171c ↗
29. 10.1021/acsanm.0c0005710.1021/acsanm.0c00057 ↗
30. 10.1021/ja077098310.1021/ja0770983 ↗
31. 10.1039/D2CY00797E10.1039/D2CY00797E ↗
32. 10.1021/jacs.4c1264310.1021/jacs.4c12643 ↗
33. 10.1002/anie.20210718510.1002/anie.202107185 ↗
34. 10.1002/adfm.20241722310.1002/adfm.202417223 ↗
35. 10.1021/jacs.9b1043610.1021/jacs.9b10436 ↗
36. 10.1021/acscatal.2c0217710.1021/acscatal.2c02177 ↗
37. 10.1002/solr.20230071010.1002/solr.202300710 ↗
38. 10.1021/acs.inorgchem.4c0188310.1021/acs.inorgchem.4c01883 ↗
39. 10.1021/acs.inorgchem.0c0380110.1021/acs.inorgchem.0c03801 ↗
40. 10.1021/ic970909r10.1021/ic970909r ↗
41. 10.1021/jacs.3c0574510.1021/jacs.3c05745 ↗
42. 10.1002/marc.20160025410.1002/marc.201600254 ↗
43. 10.1107/S010876730704393010.1107/S0108767307043930 ↗
44. 10.1107/S205322961402421810.1107/S2053229614024218 ↗
45. 10.1107/S002188980804272610.1107/S0021889808042726 ↗
46. 10.1063/1.499945410.1063/1.4999454 ↗
47. 10.1021/ar200283b10.1021/ar200283b ↗
48. 10.1038/s41428-020-00399-210.1038/s41428-020-00399-2 ↗
49. 10.1524/zkri.220.5.567.6507510.1524/zkri.220.5.567.65075 ↗
50. 10.1103/PhysRevLett.77.386510.1103/PhysRevLett.77.3865 ↗
51. Frisch, M. J.; Trucks, G. W.; Schlegel, H. B.; Scuseria, G. E.; Robb, M. A.; Cheeseman, J. R.; Scalmani, G.; Barone, V.; Petersson, G. A.; Nakatsuji, H.; Li, X.; Caricato, M.; Marenich, A. V.; Bloino, J.; Janesko, B. G.; Gomperts, R.; Mennucci, B.; Hratchian, H. P.; Ortiz, J. V.; Izmaylov, A. F.; Sonnenberg, J. L.; Williams-Young, D.; Ding, F.; Lipparini, F.; Egidi, F.; Goings, J.; Peng, B.; Petrone, A.; Henderson, T.; Ranasinghe, D.; Zakrzewski, V. G.; Gao, J.; Rega, N.; Zheng, G.; Liang, W.; Hada, M.; Ehara, M.; Toyota, K.; Fukuda, R.; Hasegawa, J.; Ishida, M.; Nakajima, T.; Honda, Y.; Kitao, O.; Nakai, H.; Vreven, T.; Throssell, K.; Montgomery, J. A., Jr.; Peralta, J. E.; Ogliaro, F.; Bearpark, M.; Heyd, J. J.; Brothers, E.; Kudin, K. N.; Staroverov, V. N.; Keith, T. A.; Kobayashi, R.; Normand, J.; Raghavachari, K.; Rendell, A.; Burant, J. C.; Iyengar, S. S.; Tomasi, J.; Cossi, M.; Millam, J. M.; Klene, M.; Adamo, C.; Cammi, R.; Ochterski, J. W.; Martin, R. L.; Morokuma, K.; Farkas, O.; Foresman, J. B.; Fox, D. J. Gaussian 09 , Revision D.01; Gaussian, Inc: Wallingford, CT, 2013.
52. Burwood, R. P.; Cheetham, A. K.CSD Communication. 2016 10.5517/ccdc.csd.cc1385sb.10.5517/ccdc.csd.cc1385sb ↗
53. 10.1021/ic900425r10.1021/ic900425r ↗
54. 10.1021/jacs.2c1189610.1021/jacs.2c11896 ↗
55. 10.1021/jacs.4c1280410.1021/jacs.4c12804 ↗
56. 10.1002/pssb.1966015022410.1002/pssb.19660150224 ↗