Light Emissive Nanocomposites Containing a Blue Fluorescent Dicationic Tetraphenylethene and a Red Phosphorescent [Mo6I8(OCOC2F5)6]2− Octahedral Cluster for Optical Writing
Source abstract
Abstract
Abstract An emissive organic–inorganic hybrid material is obtained by a cationic metathesis between a blue fluorescent tetraphenylethylene‐based salt: [TPEIm2]I2, and a red‐NIR phosphorescent octahedral molybdenum cluster compound: Cs2[Mo6I8(OCOC2F5)6]. As demonstrated by Single Crystal X‐Ray Diffraction, the hybrid [TPEIm2][Mo6I8(OCOC2F5)6] crystallizes as a 2:2 dimer and emits in the red‐NIR area. Its emission properties are studied in the solid state and once embedded in poly(methylmethacrylate) by steady state and time dependent photoluminescence spectroscopy. They are further compared to the case in which the two starting salts are directly integrated in the polymer matrix. Obtained nanocomposites show evanescent UV‐2A optical writing and reading behavior, with color contrasts depending on how emitters have been introduced.
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Research context
OpenAlex topics: Nanocluster Synthesis and Applications · Inorganic Chemistry and Materials · Luminescence and Fluorescent Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
CNRS ISCR – UMR 6226 ScanMAT – UAR 2025 Université de Rennes Rennes F‐35000 France
Nikolaev Institute of Inorganic Chemistry SB RAS 3 Acad. Lavrentiev ave. Novosibirsk 630090 Russian Federation
Funding
Russian Science Foundation
References (35)
Show source-provided references
1. 10.1038/nchem.41110.1038/nchem.411 ↗
2. 10.1021/ar500033n10.1021/ar500033n ↗
3. 10.1016/j.ccr.2015.03.00410.1016/j.ccr.2015.03.004 ↗
4. 10.1021/acsnano.0c0728910.1021/acsnano.0c07289 ↗
5. 10.1016/j.jphotochemrev.2023.10065010.1016/j.jphotochemrev.2023.100650 ↗
6. 10.1021/acs.chemmater.3c0150810.1021/acs.chemmater.3c01508 ↗
7. 10.1016/j.nantod.2018.02.01210.1016/j.nantod.2018.02.012 ↗
8. 10.1016/j.mtcomm.2023.10650810.1016/j.mtcomm.2023.106508 ↗
9. 10.1016/j.mattod.2019.12.00210.1016/j.mattod.2019.12.002 ↗
10. 10.1039/C5DT03734D10.1039/C5DT03734D ↗
11. 10.1021/acsami.7b1232010.1021/acsami.7b12320 ↗
12. 10.1002/cphc.20190056910.1002/cphc.201900569 ↗
13. 10.1039/c3cc45041d10.1039/c3cc45041d ↗
14. 10.1002/chem.20240007910.1002/chem.202400079 ↗
15. 10.1002/ejic.20120040210.1002/ejic.201200402 ↗
16. 10.1021/acs.inorgchem.6b0104210.1021/acs.inorgchem.6b01042 ↗
17. 10.1021/j100374a02910.1021/j100374a029 ↗
18. 10.1021/cm950443f10.1021/cm950443f ↗
19. 10.1021/acsami.9b2305510.1021/acsami.9b23055 ↗
20. 10.1039/D1TC01229K10.1039/D1TC01229K ↗
21. 10.1021/acs.inorgchem.9b0252910.1021/acs.inorgchem.9b02529 ↗
22. 10.1039/C8BM01564C10.1039/C8BM01564C ↗
23. 10.1021/acs.inorgchem.0c0117310.1021/acs.inorgchem.0c01173 ↗
24. 10.1016/j.xphs.2022.09.01010.1016/j.xphs.2022.09.010 ↗
25. 10.1016/j.ccr.2023.21504810.1016/j.ccr.2023.215048 ↗
26. 10.1016/0022-2313(76)90017-X10.1016/0022-2313(76)90017-X ↗
27. 10.1038/1961089a010.1038/1961089a0 ↗
28. 10.1039/C1NJ20782B10.1039/C1NJ20782B ↗
29. 10.1002/chem.20210092610.1002/chem.202100926 ↗
30. 10.1039/D3CP01295F10.1039/D3CP01295F ↗
31. 10.1002/anie.20161097110.1002/anie.201610971 ↗
32. 10.1021/ja00198a04910.1021/ja00198a049 ↗
33. 10.1039/D2TC04713F10.1039/D2TC04713F ↗
34. 10.1002/chem.20180086010.1002/chem.201800860 ↗
35. 10.1039/D4TC01043D10.1039/D4TC01043D ↗