journal article·2019-07-30

Triplet–Triplet Annihilation-Based Upconversion Sensitized by a Reverse Micellar Assembly of Amphiphilic Ruthenium Complexes

Keisuke Fujimoto, Kyosuke Kawai, Shota Masuda, Toshihiro Mori, Takumi Aizawa, Toshiyasu Inuzuka, Takashi Karatsu, Masami Sakamoto, Shiki Yagai, Tetsuya Sengoku, Masaki Takahashi, Hidemi Yoda

Langmuir· Volume 35· Issue 30
Publisher page

Abstract

We have developed a new photon upconversion (UC) system utilizing a new amphiphilic sensitizer 1a that comprises a hydrophilic ruthenium complex and a lipophilic bisanthracene appendage. At concentrations higher than 5 μM in toluene, the sensitizer 1a formed a reverse micellar assembly which facilitated the triplet sensitization of 9,10-diphenylanthracene (DPA) more efficiently than homogeneously dispersed solutions to enhance the UC efficiency up to 38.2%. The Stern–Volmer analyses revealed the stepwise triplet–triplet energy transfers (TTET): (1) intramicellar energy transfer from the ruthenium core to the bisanthracene surface and (2) diffusion-dependent energy transfer from the surface to DPA. On these bases, it can be assumed that the reverse micellar assemblies accelerate the former TTET process to enhance the UC efficiency.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Luminescence and Fluorescent Materials · Molecular Sensors and Ion Detection · Porphyrin and Phthalocyanine Chemistry

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

Affiliations

Department of Applied Chemistry, Faculty of Engineering, Shizuoka University, 3-5-1 Johoku, Naka-ku, Hamamatsu 432-8561, Japan

Division of Instrumental Analysis, Life Science Research Center, Gifu University, 1-1 Yanagido, Gifu 501-1193, Japan

Funding

Ministry of Education, Culture, Sports, Science and Technology

References (27)

Show source-provided references
1. 10.1016/j.ccr.2018.02.01110.1016/j.ccr.2018.02.011 ↗
2. 10.1039/c1ra00665g10.1039/c1ra00665g ↗
3. 10.1016/j.ccr.2010.01.00310.1016/j.ccr.2010.01.003 ↗
4. 10.1039/c1ee01659h10.1039/c1ee01659h ↗
5. 10.1038/s41586-018-0835-210.1038/s41586-018-0835-2 ↗
6. 10.1021/ja300363810.1021/ja3003638 ↗
7. 10.1039/b506575e10.1039/b506575e ↗
8. 10.1021/ja904696n10.1021/ja904696n ↗
9. 10.1021/ja411316s10.1021/ja411316s ↗
10. 10.1002/chem.20180400110.1002/chem.201804001 ↗
11. 10.1021/ja511061h10.1021/ja511061h ↗
12. 10.1038/ncomms895410.1038/ncomms8954 ↗
13. 10.1039/c6ra07666a10.1039/c6ra07666a ↗
14. 10.1002/anie.20100619210.1002/anie.201006192 ↗
15. 10.1002/chem.20110137710.1002/chem.201101377 ↗
16. 10.1002/anie.20100813410.1002/anie.201008134 ↗
17. 10.1021/jz402311j10.1021/jz402311j ↗
18. 10.1016/j.tet.2011.10.02110.1016/j.tet.2011.10.021 ↗
19. 10.1021/jp044444j10.1021/jp044444j ↗
20. 10.1562/0031-8655(2002)0750327fqyatr2.0.co210.1562/0031-8655(2002)0750327fqyatr2.0.co2 ↗
21. 10.1002/ejic.20170054810.1002/ejic.201700548 ↗
22. 10.1021/ma202804u10.1021/ma202804u ↗
23. 10.1016/j.tet.2014.10.03410.1016/j.tet.2014.10.034 ↗
24. 10.1351/pac-con-13-03-0410.1351/pac-con-13-03-04 ↗
25. 10.1021/ja058541h10.1021/ja058541h ↗
26. 10.1016/j.tetlet.2009.08.13010.1016/j.tetlet.2009.08.130 ↗
27. 10.1016/j.jphotochem.2008.12.02210.1016/j.jphotochem.2008.12.022 ↗