N,N,N-Triethyl-4-(1H-pyrrol-1-yl)butan-1-aminium Perchlorate

被引:0
|
作者
Potapenkov, Vasiliy V. [1 ]
Levin, Oleg V. [1 ]
Lukyanov, Daniil A. [1 ]
机构
[1] St Petersburg State Univ, Inst Chem, St Petersburg 199034, Russia
基金
俄罗斯科学基金会;
关键词
pyrrole; linker; ion exchange; alkylation; solubilization; POLYMERS;
D O I
10.3390/M1643
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Polypyrroles attract significant attention as the promising class of conductive polymers for the organic electronics, electrochemical energy-storage, photovoltaics, sensing and light-emitting devices due to their electrochemical and electrical properties. The attachment of the charged fragments to the pyrrole monomeric unit opens the route to a water-soluble polypyrrole for improved solution processability. Here we report a scalable multigram synthesis of the N-substituted cationic pyrrole, N,N,N-triethyl-4-(1H-pyrrol-1-yl)butan-1-aminium perchlorate, which can be used for the preparation of the water-soluble cationic polypyrrole, in two steps with 81% overall yield. The resulting product was characterized by the H-1 and C-13, nuclear magnetic resonance (NMR), ESI-high-resolution mass spectrometry (ESI-HRMS) and Fourier-transform infrared spectroscopy (FTIR).
引用
收藏
页数:4
相关论文
共 50 条
  • [1] Multielectrochromic property of N-phenylnaphthalen-2-amine and N-(4-(1H-pyrrol-1-yl)phenyl)-N-phenylnaphthalen-2-amine
    Zhang, Cheng
    Wang, Genghao
    Ouyang, Mi
    JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2011, 660 (01) : 45 - 49
  • [2] Study on Electrochromic Performance of the Copolymer Based on 4-(1H-pyrrol-1-yl) phenyl 4-(1H-pyrrol-1-yl) Butanoate with 3,4-ethylenedioxythiophene
    Ouyang, Mi
    Lv, Xiaojing
    Hu, Bin
    Zhang, Cheng
    ADVANCED MATERIALS AND STRUCTURES, PTS 1 AND 2, 2011, 335-336 : 929 - 933
  • [3] ANTIHYPERTENSIVES - N-1H-PYRROL-1-YL-3-PYRIDAZINAMINES
    BELLASIO, E
    CAMPI, A
    DIMOLA, N
    BALDOLI, E
    JOURNAL OF MEDICINAL CHEMISTRY, 1984, 27 (08) : 1077 - 1083
  • [4] Dithiophosphonation of 4-(1H-pyrrol-1-yl)phenol and 4-(1H-imidazol-1-yl)phenol
    I. S. Nizamov
    E. N. Nikitin
    E. S. Batyeva
    I. D. Nizamov
    M. P. Shulaeva
    O. K. Pozdeev
    R. A. Cherkasov
    Russian Journal of Organic Chemistry, 2015, 51 : 1272 - 1276
  • [5] Butan-1-aminium tetrachloridoferrate(III)-18-crown-6 (1/1)
    Zhang, Yuan
    ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, 2013, 69 : M38 - +
  • [6] Dithiophosphonation of 4-(1H-pyrrol-1-yl)phenol and 4-(1H-imidazol-1-yl)phenol
    Nizamov, I. S.
    Nikitin, E. N.
    Batyeva, E. S.
    Nizamov, I. D.
    Shulaeva, M. P.
    Pozdeev, O. K.
    Cherkasov, R. A.
    RUSSIAN JOURNAL OF ORGANIC CHEMISTRY, 2015, 51 (09) : 1272 - 1276
  • [7] Crystal structure of (E)-N-{[3-methyl-1pheny-l- 5-(1H-pyrrol-1-yl)-1H-pyrazol-4yl] methylidene} hydroxylamine
    Mague, Joel T.
    Mohamed, Shaaban K.
    Akkurt, Mehmet
    Ei-Emary, Talaat I.
    Albayati, Mustafa R.
    ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, 2014, 70 : O - +
  • [8] In silico and in vitro Evaluation of a New N'-(2-Arylacetyl)-4-(1H-pyrrol-1-yl) benzohydrazides as Potential Antimicrobial Agents
    Mahnashi, Mater H.
    Kittur, Bhumika
    Kumar, S. R. Prem
    Alqahtani, Ali S.
    Al Ali, Amer
    Alshahrani, Mohammed Abdulrahman
    Shaikh, Ibrahim Ahmed
    Joshi, Shrinivas D.
    INDIAN JOURNAL OF HETEROCYCLIC CHEMISTRY, 2022, 32 (04) : 523 - 530
  • [9] Synthesis, Molecular Structure, Anticancer Activity, and QSAR Study of N-(aryl/heteroaryl)-4-(1H-pyrrol-1-yl)Benzenesulfonamide Derivatives
    Zolnowska, Beata
    Slawinski, Jaroslaw
    Brzozowski, Zdzislaw
    Kawiak, Anna
    Belka, Mariusz
    Zielinska, Joanna
    Baczek, Tomasz
    Chojnacki, Jaroslaw
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2018, 19 (05)
  • [10] SYNTHESIS, ANTIBACTERIAL AND ANTITUBERCULAR ACTIVITIES OF NOVEL N1-[2-(SUBSTITUTED PHENYLAMINO) ACETYL]-4-(1H-PYRROL-1-YL)-BENZOHYDRAZIDE DERIVATIVES
    Kumar, M. R. Pradeep
    Joshi, Shrinivas D.
    Dixit, Sheshagiri R.
    Kulkarni, V. H.
    INDIAN JOURNAL OF HETEROCYCLIC CHEMISTRY, 2015, 25 (01) : 37 - 44