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Visible colorimetric dosimetry of UV and ionizing radiations by a dual-module photochromic nanocluster
Radiation dosimeters displaying conspicuous response of irradiance are highly desirable, owing to the growing demand of monitoring high-energy radiation and environmental exposure. Herein, we present a case of dosimetry based on a discrete nanocluster, [Th(6)(OH)(4)(O)(4)(H(2)O)(6)](TPC)(8)(HCOO)(4)...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8121945/ https://www.ncbi.nlm.nih.gov/pubmed/33990611 http://dx.doi.org/10.1038/s41467-021-23190-0 |
Sumario: | Radiation dosimeters displaying conspicuous response of irradiance are highly desirable, owing to the growing demand of monitoring high-energy radiation and environmental exposure. Herein, we present a case of dosimetry based on a discrete nanocluster, [Th(6)(OH)(4)(O)(4)(H(2)O)(6)](TPC)(8)(HCOO)(4)∙4DMF∙H(2)O (Th-SINAP-100), by judiciously incorporating heavy Th(6) polynuclear centers as radiation attenuator and organic linkers as photo-responsive sensor. Interestingly, dual-module photochromic transitions upon multiple external stimuli including UV, β-ray, and γ-ray are integrated into this single material. The striking color change, and more significantly, the visible color transition of luminescence in response to accumulating radiation dose allow an on-site quantitative platform for naked-eye detection of ionization radiations over a broad range (1–80 kGy). Single crystal X-ray diffraction and density functional theory calculations reveal that the dual-module photochromism can be attributed to the π(TPC) → π*(TPC) intermolecular charge transfer driven by enhanced π-π stacking interaction between the adjacent TPC moieties upon irradiation. |
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