Multicomponent Polymerizations of Isocyanides, Aldehydes, and 2-Aminopyridine toward Imidazo[1,2-a]pyridine-Containing Fused Heterocyclic Polymers

被引:6
|
作者
Chen, Tingting [1 ]
Ye, Fan [1 ]
Hu, Rongrong [1 ]
Tang, Ben Zhong [1 ,2 ,3 ]
机构
[1] South China Univ Technol, Guangdong Prov Key Lab Luminescence Mol Aggregates, State Key Lab Luminescent Mat & Devices, Guangzhou 510640, Peoples R China
[2] Chinese Univ Hong Kong, Shenzhen Inst Aggregate Sci & Technol, Sch Sci & Engn, Shenzhen 518172, Guangdong, Peoples R China
[3] AIE Inst, Guangzhou 510530, Peoples R China
基金
中国国家自然科学基金;
关键词
CONJUGATED POLYMERS; PYRAZINES; PYRIDINES;
D O I
10.1021/acs.macromol.2c01136
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In the pursuit of advanced functional polymer materials, polymers with fused heterocycles have received tremendous attention owing to their unique photoelectric proper-ties, good thermal properties, stimuli-responsive properties, and high refractive indices. However, their synthesis mainly relies on fused heterocycle-containing monomers and precursors, which has hindered the exploration of new polymer materials. Herein, transition-metal-catalyst-free multicomponent polymerizations (MCPs) of diisocyanides, dialdehydes, and 2-aminopyridine in ethanol were developed, which were featured with high efficiency and specificity, high atom economy, environmental benefits, and product structural diversity. The MCPs could not only generate long polymer chains but also build the fused heterocycle, imidazo[1,2-a]pyridine, from simple monomers, demonstrating great synthetic efficiency and simplicity. Six imidazo[1,2-a]pyridine-containing polymers with high molecular weights (Mw up to 41,700 g/mol) were obtained in high yields (up to 98%), which generally possessed good solubility, high thermal stability, unique fluorescence property, and acid/base-triggered reversible fluorescence switch behavior. The MCPs have provided an effective approach for the construction of functional polymers with complex structures, which may accelerate the development of fused heterocyclic polymer materials.
引用
收藏
页码:8590 / 8598
页数:9
相关论文
共 33 条
  • [1] Iodine mediated oxidative cross coupling of 2-aminopyridine and aromatic terminal alkyne: a practical route to imidazo[1,2-a]pyridine derivatives
    Samanta, Surya Kanta
    Bera, Mrinal K.
    ORGANIC & BIOMOLECULAR CHEMISTRY, 2019, 17 (26) : 6441 - 6449
  • [2] Copper-Catalyzed Annulation of Electrophilic Benzannulated Heterocycles with 2-Aminopyridine and 2-Aminoquinoline: Direct Access toward Polyring-Fused Imidazo[1,2-a]pyridines
    Babu, Sheba Ann
    Varsha, P. V.
    Poulose, Susanna
    Varughese, Sunil
    John, Jubi
    JOURNAL OF ORGANIC CHEMISTRY, 2023, 88 (14): : 10027 - 10039
  • [3] Self-Assembling 3-[2-Pyridylamino(phenyl)methyl]imidazo-[1,2-a]pyridine from phenylpropynal and 2-aminopyridine
    A. V. Mareev
    A. S. Medvedeva
    I. V. Mitroshina
    A. V. Afonin
    I. A. Ushakov
    G. V. Romanenko
    E. V. Tret’yakov
    Russian Journal of Organic Chemistry, 2008, 44 : 1718 - 1720
  • [4] Self-Assembling 3-[2-Pyridylamino(phenyl)methyl]imidazo-[1,2-a]pyridine from phenylpropynal and 2-aminopyridine
    Mareev, A. V.
    Medvedeva, A. S.
    Mitroshina, I. V.
    Afonin, A. V.
    Ushakov, I. A.
    Romanenko, G. V.
    Tret'yakov, E. V.
    RUSSIAN JOURNAL OF ORGANIC CHEMISTRY, 2008, 44 (11) : 1718 - 1720
  • [5] Synthesis of imidazo[1,2-a]pyridine-containing peptido- mimetics by tandem of Groebke-Blackburn-Bienayme and Ugi reactions
    Kolomiiets, Oleksandr, V
    Tsygankov, Alexander, V
    Kornet, Maryna N.
    Brazhko, Aleksander A.
    Musatov, Vladimir I.
    Chebanov, Valentyn A.
    BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY, 2023, 19 : 727 - 735
  • [6] CONVENIENT SYNTHESIS METHOD OF PHOSPHORO-CONTAINING HETEROCYCLIC-SYSTEMS OF IMIDAZO[2,1-B]THIAZOLS, IMIDAZO[1,2-A]PYRIDINES AND IMIDAZO[1,2-A]QUINOXALINES
    YAGODINETS, PI
    CHERNYUK, IN
    SHEVCHUK, MI
    ZHURNAL OBSHCHEI KHIMII, 1984, 54 (12): : 2789 - 2790
  • [7] Synthesis of 2,6-dichloro-5-(beta-D-ribofuranosyl)imidazo[1,2-a]pyridine, the first C-nucleoside containing an imidazo[1,2-a]pyridine heterocycle as the aglycon
    Gudmundsson, KS
    Drach, JC
    Townsend, LB
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1996, 211 : 266 - ORGN
  • [8] Iodine mediated oxidative cross coupling of 2-aminopyridine and aromatic terminal alkyne: a practical route to imidazo[1,2-a]pyridine derivatives (vol 17, pg 6441, 2019)
    Samanta, Surya Kanta
    Bera, Mrinal K.
    ORGANIC & BIOMOLECULAR CHEMISTRY, 2019, 17 (31) : 7425 - 7425
  • [9] Copper-catalyzed tandem cyclization of 2-(2-iodophenyl)imidazo[1,2-a] pyridine derivatives with selenium: Synthesis of benzo[b]selenophene-fused imidazo[1,2-a]pyridines
    Matsumura, Mio
    Sakata, Yumi
    Iwase, Atsuya
    Kawahata, Masatoshi
    Kitamura, Yuki
    Murata, Yuki
    Kakusawa, Naoki
    Yamaguchi, Kentaro
    Yasuike, Shuji
    TETRAHEDRON LETTERS, 2016, 57 (49) : 5484 - 5488
  • [10] NOVEL CONDENSATION OF 2,3-EPOXYBUTANAL WITH 2-AMINOPYRIDINE AND 2-AMINOPYRAZINE - SYNTHESIS AND STABILITY OF 3-(1-HYDROXYETHYL)IMIDAZO[1,2-A]AZINES
    LUMMA, WC
    SPRINGER, JP
    JOURNAL OF ORGANIC CHEMISTRY, 1981, 46 (18): : 3735 - 3736