Fine‐Tuning X‐Ray Sensitivity in Organic–Inorganic Hybrids via an Unprecedented Mixed‐Ligand Strategy
Source abstract
Abstract
Abstract Crystalline organic–inorganic hybrids, which exhibit colorimetric responses to ionizing radiation, have recently been recognized as promising alternatives to conventional X‐ray dosimeters. However, X‐ray‐responsive organic–inorganic hybrids are scarce and the strategy to fine‐tune their detection sensitivity remains elusive. Herein, an unprecedented mixed‐ligand strategy is reported to modulate the X‐ray detection efficacy of organic–inorganic hybrids. Deliberately blending the stimuli‐responsive terpyridine carboxylate ligand (tpc−) and the auxiliary pba− group with different ratios gives rise to two OD thorium‐bearing clusters (Th‐102 and Th‐103) and a 1D coordination polymer (Th‐104). Notably, distinct X‐ray sensitivity is evident as a function of molar ratio of the tpc− ligand, following the trend of Th‐102 > Th‐103 > Th‐104. Moreover, Th‐102, which is exclusively built from the tpc− ligands with the highest degree of π–π interactions, exhibits the most sensitive radiochromic and fluorochromic responses toward X‐ray with the lowest detection limit of 1.5 mGy. The study anticipates that this mixed‐ligand strategy will be a versatile approach to tune the X‐ray sensing efficacy of organic–inorganic hybrids.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Radioactive element chemistry and processing · Lanthanide and Transition Metal Complexes
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Shanghai Institute of Applied Physics Chinese Academy of Sciences 2019 Jia Luo Road Shanghai 201800 P. R. China
School of Nuclear Science and Technology Xi'an Jiaotong University No.28, West Xianning Road Xi'an 710049 P. R. China
Funding
National Natural Science Foundation of China
References (63)
Show source-provided references
1. 10.1038/s41586-021-03251-610.1038/s41586-021-03251-6 ↗
2. 10.1038/s41566-022-01024-910.1038/s41566-022-01024-9 ↗
3. 10.1126/sciadv.aaw870410.1126/sciadv.aaw8704 ↗
4. 10.1002/anie.20200638010.1002/anie.202006380 ↗
5. 10.1002/anie.20170091910.1002/anie.201700919 ↗
6. 10.1002/adfm.20220168410.1002/adfm.202201684 ↗
7. 10.1002/adfm.20160672410.1002/adfm.201606724 ↗
8. 10.1007/s11426-020-9817-910.1007/s11426-020-9817-9 ↗
9. 10.1002/anie.20201729810.1002/anie.202017298 ↗
10. 10.1021/jacs.1c1115010.1021/jacs.1c11150 ↗
11. 10.1038/nphoton.2016.4110.1038/nphoton.2016.41 ↗
12. 10.1038/nphoton.2017.4310.1038/nphoton.2017.43 ↗
13. 10.1021/jacs.0c0811710.1021/jacs.0c08117 ↗
14. 10.1038/s41566-021-00769-z10.1038/s41566-021-00769-z ↗
15. 10.1002/anie.20180286510.1002/anie.201802865 ↗
16. 10.1021/acsmaterialslett.2c0065810.1021/acsmaterialslett.2c00658 ↗
17. 10.1002/adma.20190471110.1002/adma.201904711 ↗
18. 10.1021/jacs.3c0196810.1021/jacs.3c01968 ↗
19. Andreo P. · 2017
20. 10.1002/adfm.20221290710.1002/adfm.202212907 ↗
21. 10.1039/B917890B10.1039/B917890B ↗
22. 10.1038/s41467-020-14986-710.1038/s41467-020-14986-7 ↗
23. 10.1021/jacs.0c1018310.1021/jacs.0c10183 ↗
24. 10.1002/anie.20201682610.1002/anie.202016826 ↗
25. 10.1002/ange.20221177610.1002/ange.202211776 ↗
26. 10.1021/acs.chemrev.9b0035010.1021/acs.chemrev.9b00350 ↗
27. 10.1021/jacs.2c0987910.1021/jacs.2c09879 ↗
28. 10.1021/acsami.7b1512710.1021/acsami.7b15127 ↗
29. 10.1039/D2MH00593J10.1039/D2MH00593J ↗
30. 10.1039/D0SC02540B10.1039/D0SC02540B ↗
31. 10.1021/acsnano.5b0511310.1021/acsnano.5b05113 ↗
32. 10.1016/j.matt.2022.08.01510.1016/j.matt.2022.08.015 ↗
33. 10.1021/jacs.1c1149610.1021/jacs.1c11496 ↗
34. 10.1038/s41467-021-23190-010.1038/s41467-021-23190-0 ↗
35. 10.1002/smll.20220678210.1002/smll.202206782 ↗
36. 10.1016/j.cej.2022.13546810.1016/j.cej.2022.135468 ↗
37. 10.1016/j.cej.2023.14327210.1016/j.cej.2023.143272 ↗
38. 10.1126/science.123833910.1126/science.1238339 ↗
39. 10.1021/jacs.9b1307210.1021/jacs.9b13072 ↗
40. 10.1021/acs.accounts.8b0041510.1021/acs.accounts.8b00415 ↗
41. 10.1002/anie.20141025210.1002/anie.201410252 ↗
42. 10.1002/anie.20180405910.1002/anie.201804059 ↗
43. 10.1039/D2DT00265E10.1039/D2DT00265E ↗
44. 10.1016/j.ccr.2021.21401110.1016/j.ccr.2021.214011 ↗
45. 10.1002/anie.20130313710.1002/anie.201303137 ↗
46. 10.1002/anie.20170123510.1002/anie.201701235 ↗
47. 10.1039/D0TC04234J10.1039/D0TC04234J ↗
48. 10.1002/agt2.34410.1002/agt2.344 ↗
49. 10.1002/anie.20200400610.1002/anie.202004006 ↗
50. 10.1063/5.013498210.1063/5.0134982 ↗
51. 10.1039/D1CC02649F10.1039/D1CC02649F ↗
52. 10.1021/acs.chemmater.1c0299910.1021/acs.chemmater.1c02999 ↗
53. 10.1021/acs.chemmater.2c0217010.1021/acs.chemmater.2c02170 ↗
54. 10.1021/jacs.1c0885410.1021/jacs.1c08854 ↗
55. 10.1039/D1SC01827B10.1039/D1SC01827B ↗
56. 10.1021/acs.iecr.9b0682010.1021/acs.iecr.9b06820 ↗
57. 10.1002/anie.20190412110.1002/anie.201904121 ↗
58. 10.1039/C9CS00203K10.1039/C9CS00203K ↗
59. 10.1039/C1CS15126F10.1039/C1CS15126F ↗
60. 10.1039/B818330A10.1039/B818330A ↗
61. 10.1039/D1CC00614B10.1039/D1CC00614B ↗
62. 10.1039/C6SC04579K10.1039/C6SC04579K ↗
63. 10.1021/acs.chemmater.2c0366810.1021/acs.chemmater.2c03668 ↗