Effective Approach toward Selective Near-Infrared Dyes: Rational Design, Synthesis, and Characterization of Thieno[3,4-b]thiophene-Based Quinoidal Oligomers
Source abstract
Abstract
This paper describes syntheses, photophysical properties, and electrochemical characteristics of three thieno[3,4-b]thiophene (TT)-based quinoidal oligomers OnTTO. The rigid planar backbones of these oligomers give the molecules narrow absorption bands, and the main absorption bands were significantly red-shifted when the TT units were extended and demonstrated wide transparent windows. The compound O4TTO was found to possess strong absorption in the near-infrared (NIR) region approaching 1200 nm but remained transparent in the visible region. Electrochemical experiments have shown that the energy band gaps gradually narrow when the TT units are increased. Optical properties predicted by density functional theory calculations are in good agreement with the experimental optical results. These dye molecules could be promising candidates for future NIR photodetectors, filters, and bioimaging technologies.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Conducting polymers and applications · Organic Electronics and Photovoltaics · Luminescence and Fluorescent Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory of Surface and Interface Science of Polymer Materials of Zhejiang Province, Department of Chemistry, Zhejiang Sci-Tech University, 928 Second Street, Hangzhou310018, China
Department of Chemistry and the James Franck Institute, The University of Chicago, 929 E57th Street, Chicago, Illinois60637, United States
Funding
Division of Chemistry · Samsung · Zhejiang Sci-Tech University · National Natural Science Foundation of China · Natural Science Foundation of Zhejiang Province
References (23)
Show source-provided references
1. 10.1021/acs.chemrev.5b0016510.1021/acs.chemrev.5b00165 ↗
2. 10.1002/tcr.20160001310.1002/tcr.201600013 ↗
3. 10.1038/nmat192810.1038/nmat1928 ↗
4. 10.1002/aenm.20130100610.1002/aenm.201301006 ↗
5. 10.1021/ja401434x10.1021/ja401434x ↗
6. 10.1038/nphoton.2011.35610.1038/nphoton.2011.356 ↗
7. 10.1002/adma.20130494510.1002/adma.201304945 ↗
8. 10.1002/adfm.20130053610.1002/adfm.201300536 ↗
9. 10.1021/cr078381n10.1021/cr078381n ↗
10. 10.1039/C5CS00030K10.1039/C5CS00030K ↗
11. 10.1021/ja00130a02410.1021/ja00130a024 ↗
12. 10.1039/C8SC04363A10.1039/C8SC04363A ↗
13. 10.1016/j.trechm.2019.03.00210.1016/j.trechm.2019.03.002 ↗
14. 10.1021/acs.macromol.9b0265310.1021/acs.macromol.9b02653 ↗
15. 10.1021/ja901545q10.1021/ja901545q ↗
16. 10.1002/adma.20090352810.1002/adma.200903528 ↗
17. 10.1039/D0TC01257B10.1039/D0TC01257B ↗
18. 10.1039/C8TC01802B10.1039/C8TC01802B ↗
19. 10.1039/D0TC00269K10.1039/D0TC00269K ↗
20. 10.1002/chem.20170600210.1002/chem.201706002 ↗
21. 10.1016/S0379-6779(99)00007-710.1016/S0379-6779(99)00007-7 ↗
22. 10.1021/jacs.6b0356210.1021/jacs.6b03562 ↗
23. 10.1021/acs.chemmater.6b0428710.1021/acs.chemmater.6b04287 ↗