journal article·2021

End-functionalization of dithiarubicene: modulation of optoelectronic properties by metal-catalyzed coupling reactions and device application

Kenji Tsukamoto, Koji Takagi, Keitaro Yamamoto, Yutaka Ie, Takanori Fukushima

Journal of Materials Chemistry C· Volume 9· Issue 18
Publisher page

Abstract

In order to modulate the optoelectronic properties of dithiarubicene ( DTR ) by end-functionalization and reveal the structure–property relationship in detail, we have carried out a set of metal-catalyzed coupling reactions.
Only a short abstract or summary was supplied by the source.
Source: crossref · Quality: short

Research context

OpenAlex topics: Organic Light-Emitting Diodes Research · Organic Electronics and Photovoltaics · Perovskite Materials and Applications

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

Affiliations

Graduate School of Engineering

Nagoya Institute of Technology

Nagoya 466-8555

Japan

The Institute of Scientific and Industrial Research (ISIR)

Osaka University

Ibaraki

Laboratory of Chemistry and Life Science Institute of Innovative Research

Tokyo Institute of Technology

Yokohama 226-8503

Funding

Osaka University

References (43)

Show source-provided references
1. Allard · Angew. Chem., Int. Ed. · 2008 · 47 · 407010.1002/anie.200701920 ↗
2. Chen · Acc. Chem. Res. · 2013 · 46 · 264510.1021/ar400088c ↗
3. Kang · Chem. Sci. · 2010 · 1 · 17910.1039/c0sc00156b ↗
4. Kang · Adv. Mater. · 2011 · 23 · 122210.1002/adma.201001283 ↗
5. Sawamoto · ACS Appl. Mater. Interfaces · 2016 · 8 · 381010.1021/acsami.5b10477 ↗
6. Kawabata · J. Org. Chem. · 2020 · 85 · 19510.1021/acs.joc.9b02585 ↗
7. Lee · Adv. Mater. · 2011 · 23 · 535910.1002/adma.201103177 ↗
8. Wu · ACS Appl. Mater. Interfaces · 2017 · 9 · 1496710.1021/acsami.7b01702 ↗
9. Ghosh · ACS Appl. Mater. Interfaces · 2019 · 11 · 108810.1021/acsami.8b16714 ↗
10. Thalacker · J. Org. Chem. · 2006 · 71 · 809810.1021/jo0612269 ↗
11. Shukla · Org. Lett. · 2018 · 20 · 786410.1021/acs.orglett.8b03408 ↗
12. Chang · Org. Lett. · 2012 · 14 · 296410.1021/ol300914k ↗
13. Kumar · J. Am. Chem. Soc. · 2014 · 136 · 1200410.1021/ja504903j ↗
14. Shukla · Chem. Commun. · 2018 · 54 · 90010.1039/C7CC09372A ↗
15. Asthana · Chem. Commun. · 2012 · 48 · 647510.1039/c2cc31274c ↗
16. Keshri · Chem. – Eur. J. · 2018 · 24 · 182110.1002/chem.201704604 ↗
17. Mohebbi · Chem. – Eur. J. · 2011 · 17 · 264210.1002/chem.201002608 ↗
18. Tsukamoto · J. Mater. Chem. C · 2019 · 7 · 1261010.1039/C9TC04325J ↗
19. Lee · J. Mater. Chem. C · 2014 · 2 · 336110.1039/C3TC32117G ↗
20. Mohebbi · Adv. Mater. · 2011 · 23 · 464410.1002/adma.201102726 ↗
21. Wang · Angew. Chem., Int. Ed. · 2012 · 51 · 692010.1002/anie.201201796 ↗
22. Chaolumen · Org. Lett. · 2017 · 19 · 82610.1021/acs.orglett.6b03819 ↗
23. Herges · J. Phys. Chem. A · 2001 · 105 · 321410.1021/jp0034426 ↗
24. Geuenich · Chem. Rev. · 2005 · 105 · 375810.1021/cr0300901 ↗
25. Chang · Org. Lett. · 2012 · 14 · 296410.1021/ol300914k ↗
26. Zhao · Mater. Chem. Front. · 2017 · 1 · 163510.1039/C7QM00030H ↗
27. Zanon · J. Am. Chem. Soc. · 2003 · 125 · 289010.1021/ja0299708 ↗
28. Andreeva · Chem. Heterocycl. Compd. · 2018 · 54 · 61210.1007/s10593-018-2316-9 ↗
29. Rosenmund · Chem. Ber. · 1919 · 52 · 174910.1002/cber.19190520840 ↗
30. Pongratz · Monatsh. Chem. · 1927 · 48 · 58510.1007/BF01518076 ↗
31. von Braun · Liebigs Ann. Chem. · 1931 · 488 · 11110.1002/jlac.19314880107 ↗
32. Prim · Tetrahedron · 2002 · 58 · 204110.1016/S0040-4020(02)00076-5 ↗
33. Evano · Chem. Rev. · 2008 · 108 · 305410.1021/cr8002505 ↗
34. Guo · Eur. J. Org. Chem. · 2015 · 474410.1002/ejoc.201500500 ↗
35. Keegstra · Tetrahedron · 1992 · 48 · 363310.1016/S0040-4020(01)88501-X ↗
36. Chen · J. Am. Chem. Soc. · 2019 · 141 · 354110.1021/jacs.8b12142 ↗
37. Sice · J. Am. Chem. Soc. · 1953 · 75 · 369710.1021/ja01111a027 ↗
38. Higuchi · Bull. Chem. Soc. Jpn. · 1998 · 71 · 48310.1246/bcsj.71.483 ↗
39. Perrin · Eur. J. Org. Chem. · 2011 · 542710.1002/ejoc.201100513 ↗
40. Kishore · J. Am. Chem. Soc. · 2009 · 131 · 1110610.1021/ja9030648 ↗
41. Waldrip · Adv. Funct. Mater. · 2020 · 30 · 190457610.1002/adfm.201904576 ↗
42. Xu · ACS Appl. Mater. Interfaces · 2014 · 6 · 1449310.1021/am5037862 ↗
43. Li · Chem. Mater. · 2014 · 26 · 578210.1021/cm502952u ↗