Functionalization of Carboxylated Multi-Wall Nanotubes with Derivatives of N1-(11H-Indeno[1,2-b]quinoxalin-11-ylidene)benzene-1,4-diamine

被引:2
|
作者
Azizian, Javad [1 ]
Zomorodbakhsh, Shahab [2 ]
Entezari, Mahdieh [1 ]
Anaraki-Ardakani, Hossein [2 ]
机构
[1] Islamic Azad Univ, Sci & Res Branch, Dept Chem, Tehran, Iran
[2] Islamic Azad Univ, Mahshahr Branch, Dept Chem, Mahshahr, Iran
关键词
CARBON NANOTUBES;
D O I
10.1155/2013/917970
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Quinoxaline derivatives are compounds with pharmaceutical applications. In this study, derivatives of N1-(11H-indeno[1,2-b]quinoxalin-11-ylidene)benzene-1,4-diamine were synthesized and attached to carboxylated multi-wall nanotubes (MWNT-COOH). Functionalized carbon nanotubes were characterized by scanning electron microscopy (SEM) to study the shape of structures, transmission electron microscopy (TEM), fast Fourier trnasfrom infrared (FT-IR), Raman spectroscopy, and elemental analysis.
引用
收藏
页数:7
相关论文
共 50 条
  • [31] A highly diastereoselective one-pot three-component 1,3-dipolar cycloaddition of cyclopropenes with azomethine ylides generated from 11H-indeno[1,2-b]-quinoxalin-11-ones
    Filatov, A. S.
    Knyazev, N. A.
    Ryazantsev, M. N.
    Suslonov, V. V.
    Larina, A. G.
    Molchanov, A. P.
    Kostikov, R. R.
    Boitsov, V. M.
    Stepakov, A. V.
    ORGANIC CHEMISTRY FRONTIERS, 2018, 5 (04): : 595 - 605
  • [32] Iridium(III) and Rhodium(III) Half-Sandwich Coordination Compounds with 11H-Indeno[1,2-b]quinoxalin-11-one Oxime: A Case of Spontaneous Resolution of Rh(III) Complex
    Matveevskaya, Vladislava V.
    Pavlov, Dmitry, I
    Potapov, Andrei S.
    INORGANICS, 2022, 10 (11)
  • [33] ANALGESIC AND ANTIINFLAMMATORY ACTIVITY OF 10-AMINO-11H-INDENO [1,2-B] QUINOLIN-11-ONE DERIVATIVES
    BALA, M
    NAPARZEWSKA, A
    CHOJNACKAWOJCIK, E
    POLISH JOURNAL OF PHARMACOLOGY AND PHARMACY, 1986, 38 (02): : 221 - 227
  • [34] An Efficient Regioselective Access to (11Z)-11-(3-Aryl-5,6-dihydropyrazin-2(1H)-ylidene)-11H-indeno[1,2-b] quinoxaline Derivatives via One-Pot Three-Component Reaction
    Alizadeh, Abdolali
    Roosta, Atefeh
    CHEMISTRYSELECT, 2019, 4 (46): : 13503 - 13505
  • [35] Synthesis of 9H-Indeno [1, 2-b] Pyrazine and 11H-Indeno [1, 2-b] Quinoxaline Derivatives in One-step Reaction from 2-Bromo-4-chloro-1-indanone
    Jasouri, S.
    Khalafy, J.
    Badali, M.
    Prager, R. H.
    SOUTH AFRICAN JOURNAL OF CHEMISTRY-SUID-AFRIKAANSE TYDSKRIF VIR CHEMIE, 2011, 64 : 105 - 107
  • [36] Blue Fluorescent Organic Light-Emitting Diodes Using 11,11-Dimethy1-3-(10-phenylanthracen-9-yl)-11H-Indeno[1,2-b]Quinoline Derivatives
    Moon, Junyoung
    Lee, Jinho
    Kim, Ki Ju
    Lee, Hakjun
    Kim, Young Kwan
    Yoon, Seung Soo
    JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY, 2020, 20 (08) : 4652 - 4656
  • [37] I2/p-TSA: An efficient reagent for regioselective synthesis of angularly fused diazabenzocyclo-pentafluorene via iodocyclisation of 11-(arylethynyl)-11H-indeno[1,2-b]quinoxalin-11-ol
    Padmashrija, Ammundi Jayavel Chirranjeevi
    Kannadasan, Sathananthan
    Shanmugam, Ponnusamy
    TETRAHEDRON LETTERS, 2025, 156
  • [38] Experimental and Computational Investigation of the Oxime Bond Stereochemistry in c-Jun N-terminal Kinase 3 Inhibitors 11H-Indeno[1,2-b]quinoxalin-11-one Oxime and Tryptanthrin-6-oxime
    Matveevskaya, Vladislava V. V.
    Pavlov, Dmitry I. I.
    Kovrizhina, Anastasia R. R.
    Sukhikh, Taisiya S. S.
    Sadykov, Evgeniy H. H.
    Dorovatovskii, Pavel V. V.
    Lazarenko, Vladimir A. A.
    Khlebnikov, Andrei I. I.
    Potapov, Andrei S. S.
    PHARMACEUTICS, 2023, 15 (07)
  • [39] Biradicals/zwitterions from enallene-isonitriles.: Formal [4+1] cycloadditions leading to 11H-indeno[1,2-b]quinoline and related compounds
    Lu, XL
    Petersen, JL
    Wang, KK
    ORGANIC LETTERS, 2003, 5 (18) : 3277 - 3280
  • [40] 1 ',1 ''-Dimethyl-4 '-phenyldispiro[11H-indeno[1,2-b]quinoxaline-11,2 '-pyrrolidine-3 ',3 ''-piperidin]-4 ''-one
    Suresh, J.
    Nagalakshmi, R. A.
    Malathi, K.
    Kumar, R. R.
    Lakshman, P. L. N.
    ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, 2013, 69 : O1433 - +