Synthsis of [1,2,5]thiadiazolo[3,4-c]pyridine: A Novel analogue to BT

被引：4
|
作者：
Sun Xiaoxia [1 ]
Lou Yazhou [1 ]
Chen Qiangqiang [1 ]
Li Li [1 ]
Zhuang Xiaoxiao [1 ]
Li Yingchun [1 ]
机构：
[1] Jiangxi Sci & Technol Normal Univ, Jiangxi Key Lab Organ Chem, Nanchang 330013, Peoples R China
来源：
ADVANCED MATERIALS AND STRUCTURES, PTS 1 AND 2 | 2011年 / 335-336卷
关键词：
Low-Bandgap; Donor-acceptor; light-emitting devices; ACCEPTOR CONJUGATED COPOLYMERS; ELECTRONIC-STRUCTURE; POLYMER;
D O I：
10.4028/www.scientific.net/AMR.335-336.90
中图分类号：
T [工业技术];
学科分类号：
08 ;
摘要：
Heterocyclic electron-poor monomer [1,2,5]thiadiazolo[3,4-c]pyridine have been synthesized in high yields over five steps from readily available starting materials. The new deficient acceptor has good solubility in organic solvents so as to permit an appropriate coating process.
引用
收藏
页码：90 / 95
页数：6
相关论文
共 50 条
  • [21] Facile synthsis and evaluation of antitumor and antiviral activities of [1,2,5]thiadiazolo[3,4-d]-pyrimidines (8-thiapurines) and 4-β-D-ribofuranosyl-[1,2,5]thiadiazolo[3,4-d]pyrimidines
    Nagamatsu, Tomohisa
    Islam, Rafiqul
    Ashida, Noriyuki
    HETEROCYCLES, 2007, 72 : 573 - 588
  • [22] SYNTHESIS AND CHARACTERIZATION OF THIENO[3,4-C][1,2,5]THIADIAZOLES
    TANAKA, S
    TOMURA, M
    YAMASHITA, Y
    HETEROCYCLES, 1994, 37 (02) : 693 - 696
  • [23] (1,2,5)THIADIAZOLE(3,4-C)(1,2,5)THIADIAZOLE, C2N4S2
    KANE, J
    SCHAEFFER, R
    CRYSTAL STRUCTURE COMMUNICATIONS, 1981, 10 (04): : 1403 - 1404
  • [24] On the nucleophilic derivatization of 4,7-dibromo-[1,2,5]thiadiazolo[3,4-c]pyridine: basis for biologically interesting species and building blocks for organic materials
    Gonzalez-Antonio, Oscar
    Navarro Villalobos, Mauricio
    Magdalena Vazquez-Alvarado, Maria
    Santillan, Rosa
    Flores-Perez, Bias
    Romero-Avila, Margarita
    Farfan, Norberto
    NEW JOURNAL OF CHEMISTRY, 2019, 43 (26) : 10491 - 10500
  • [25] NON-CLASSICAL THIENO [3,4-C] [1,2,5] THIADIAZOLE
    BEHFOROUZ, M
    BENRASHID, R
    TETRAHEDRON LETTERS, 1979, (46) : 4493 - 4494
  • [26] Synthesis and photovoltaic properties of new [1,2,5]thiadiazolo[3,4-c]pyridine-based organic Broadly absorbing sensitizers for dye-sensitized solar cells
    Ying, Weijiang
    Zhang, Xiaoyu
    Li, Xin
    Wu, Wenjun
    Guo, Fuling
    Li, Jing
    Agren, Hans
    Hua, Jianli
    TETRAHEDRON, 2014, 70 (25) : 3901 - 3908
  • [27] Tetraphenylethene end-capped [1,2,5]thiadiazolo[3,4-c]pyridine with aggregation-induced emission and large two-photon absorption cross-sections
    Jiang, Tao
    Qu, Yi
    Li, Bo
    Gao, Yuting
    Hua, Jianli
    RSC ADVANCES, 2015, 5 (02) : 1500 - 1506
  • [28] Effective synthesis of 4,5-dibromobenzo[1,2-c:3,4-c']-bis([1,2,5]thiadiazole) by bromination of benzo[1,2-c:3,4-c']-bis([1,2,5]thiadiazole)
    Chechulina, Alexandra S.
    Konstantinova, Lidia S.
    Obruchnikova, Natalia V.
    Knyazeva, Ekaterina A.
    Kan, Bin
    Duan, Tainan
    Chen, Yongsheng
    Aysin, Rinat A.
    Rakitin, Oleg A.
    CHEMISTRY OF HETEROCYCLIC COMPOUNDS, 2024, 60 (7-8) : 403 - 408
  • [29] Synthesis and reactivity of [1,2,5]thiadiazolo[3,4-b]pyridines and [1,2,5]selenadiazolo[3,4-b]pyridines (microreview)
    Bastrakov, Maxim A.
    Ivanova, Victoria V.
    CHEMISTRY OF HETEROCYCLIC COMPOUNDS, 2024, 60 (1-2) : 38 - 40
  • [30] 4,7-Bis(2,3,3a,8b-tetrahydrocyclopenta[b]indol-4(1H)-yl)-[1,2,5]thiadiazolo[3,4-c]pyridine
    Chmovzh, Timofey N.
    Rakitin, Oleg A.
    MOLBANK, 2022, 2022 (03)
12345