4,7-Bis(5-(9-hexyl-9H-carbazol-3-yl)thiophen-2-yl)-[1,2,5]thiadiazolo[3,4-d]pyridazine

4,7-Bis(5-(9-hexyl-9H-carbazol-3-yl)thiophen-2-yl)-[1,2,5]thiadiazolo[3,4-d]pyridazine Full article

Journal

Molbank
ISSN: 1422-8599

Output data

Year: 2022, Volume: 2022, Number: 1, Article number : M1332, Pages count : DOI: 10.3390/m1332

Authors

Chmovzh Timofey ^1,2 , Korshunov Vladislav ³ , Taydakov Ilya ³ , Rakitin Oleg ¹

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky Prospekt, 119991 Moscow, Russia
2	Nanotechnology Education and Research Center, South Ural State University, 76 Lenina Avenue, 454080 Chelyabinsk, Russia
3	P. N. Lebedev Physical Institute of the Russian Academy of Sciences, 53 Leninsky Prospect, 119991 Moscow, Russia

Donor molecules of the D-π-A-π-D type structure are often used for applications in organic photovoltaics. In this communication, bromination of 4,7-di(thiophen-2-yl)-[1,2,5]thiadiazolo[3,4-d]pyridazine followed by Suzuki cross-coupling with carbazoleboronic acid gave 4,7-bis( 5-(9-hexyl-9H-carbazol-3-yl)thiophen-2-yl)-[1,2,5]thiadiazolo[3,4-d]pyridazine. The structure of the newly synthesized compounds was established by high resolution mass-spectrometry, 1H, 13C NMR, IR, and UV spectroscopy and mass-spectrometry. A study of the luminescent properties of the dye showed that it exhibits fluorescence in the near infrared region of the spectrum, which makes it a promising compound for use as an active emitting layer in NIR OLED as well as for other possible applications as an IR luminophore.

Chmovzh T. , Korshunov V. , Taydakov I. , Rakitin O.
4,7-Bis(5-(9-hexyl-9H-carbazol-3-yl)thiophen-2-yl)-[1,2,5]thiadiazolo[3,4-d]pyridazine
Molbank. 2022. V.2022. N1. M1332 . DOI: 10.3390/m1332 WOS Scopus OpenAlex

Web of science:	WOS:000774150200001
Scopus:	2-s2.0-85124527128
OpenAlex:	W4211133710

DB	Citing
OpenAlex	Нет цитирований
Scopus	Нет цитирований