Bromination of naphtho[2,3-c][1,2,5]thiadiazole-4,9-dione

被引：0

作者：

Konstantinova, L. S. ^{[1
]}

Chechulina, A. S. ^{[1
]}

Obruchnikova, N. V. ^{[1
]}

Knyazeva, E. A. ^{[1
]}

Kan, Bin ^{[2
]}

Duan, Tainan ^{[3
,4
]}

Chen, Yongsheng ^{[3
,4
]}

Rakitin, O. A. ^{[1
]}

机构：

[1] Russian Acad Sci, ND Zelinsky Inst Organ Chem, 47 Leninsky prosp, Moscow 119991, Russia

[2] Nankai Univ, Natl Inst Adv Mat, Sch Mat Sci & Engn, Tianjin 300350, Peoples R China

[3] Nankai Univ, Ctr Nanoscale Sci & Technol, State Key Lab Elemento Organ Chem, Tianjin 300071, Peoples R China

[4] Nankai Univ, Coll Chem, Renewable Energy Convers & Storage Ctr RECAST, Key Lab Funct Polymer Mat, Tianjin 300071, Peoples R China

来源：

RUSSIAN CHEMICAL BULLETIN | 2024年 / 73卷 / 10期

基金：

俄罗斯科学基金会;

关键词：

naphtho[2,3-c][1,2,5]thiadiazole-4,9-dione; bromination; non-fullerene acceptors;

D O I：

10.1007/s11172-024-4420-6

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Investigations of bromination of naphtho[2,3-c][1,2,5]thiadiazole-4,9-dione revealed that the reaction proceeded most efficiently with N-bromosuccinimide in sulfuric acid and depending on the reaction conditions, can give mono-, di-, tri- and tetrabromo derivatives of naphtho[2,3-c][1,2,5]thiadiazole-4,9-dione. A series of the major isomers was isolated, and their structure was proven using heteronuclear multiple bond correlation NMR spectroscopy and high-resolution mass spectrometry.

引用

页码：3038 / 3044

页数：7

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