Abstract
Bright fluorescent molecules with long fluorescence lifetimes are important for the development of lifetime-based fluorescence imaging techniques. Herein, a molecular design is described for simultaneously attaining long fluorescence lifetime (τ) and high brightness (ΦF×ɛ) in a system that features macrocyclic dimerization of fluorescent π-conjugated skeletons with flexible linkers. An alkylene-linked macrocyclic dimer of bis(thienylethynyl)anthracene was found to show excimer emission with a long fluorescence lifetime (τ≈19 ns) in solution, while maintaining high brightness. A comparison with various relevant derivatives revealed that the macrocyclic structure and the length of the alkylene chains play crucial roles in attaining these properties. In vitro time-gated imaging experiments were conducted as a proof-of-principle for the superiority of this macrocyclic fluorophore relative to the commercial fluorescent dye Alexa Fluor 488.
Original language | English |
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Pages (from-to) | 7131-7135 |
Number of pages | 5 |
Journal | Angewandte Chemie - International Edition |
Volume | 55 |
Issue number | 25 |
DOIs | |
State | Published - Jun 13 2016 |
Externally published | Yes |
Funding
This work was partly supported by CREST, JST (S.Y.), and the Japan Advanced Plant Science Network. ITbM is supported by the World Premier International Research Center (WPI) Initiative, Japan. We are grateful to Dr. Naoki Yanagisawa (Nagoya Univ.) for the preparation of PDMS microfluidic devices
Funders | Funder number |
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Japan Advanced Plant Science Network | |
World Premier International Research Center | |
Japan Society for the Promotion of Science | 15F15778, 15K05385, 15H05482 |
Japan Science and Technology Agency | |
Core Research for Evolutional Science and Technology |
Keywords
- excimer
- fluorescence
- imaging agents
- photophysics
- pi conjugation