Author:
Sukhikh T.S.,Bashirov D.A.,Shuvaev S.,Komarov V.Yu.,Kuratieva N.V.,Konchenko S.N.,Benassi E.
Funder
RFBR
the Ministry of Education and Science of the Russian Federation
Subject
Materials Chemistry,Inorganic Chemistry,Physical and Theoretical Chemistry
Cited by
15 articles.
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1. 2,1,3-Benzothiadiazoles Are Versatile Fluorophore Building Blocks for the Design of Analyte-Sensing Optical Devices;Chemosensors;2024-08-07
2. Access to long-lived room temperature phosphorescence through auration of 2,1,3-benzothiadiazole;Dalton Transactions;2024
3. Utility of 4‐Amino‐2,1,3‐benzothiadiazole Directing Group in the Pd(II)‐catalyzed Arylation of
γ
‐C−H Bonds of Carboxamides and
β
‐C‐H Bonds of Amino Acid Carboxamides;Asian Journal of Organic Chemistry;2022-11-29
4. Chalcogen-bonded donor–acceptor complexes of 5,6-dicyano[1,2,5]selenadiazolo[3,4-b]pyrazine with halide ions;New Journal of Chemistry;2022
5. The effect of halides and coordination mode of 4-amino-2,1,3-benzothiadiazole on the luminescence properties of its Zn complexes;CrystEngComm;2022