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Chemistry of Heterocyclic Compounds

, Volume 48, Issue 9, pp 1325–1331 | Cite as

New chemosensor systems of the benzo-[de]Isoquinoline-1,3-Dione Series

  • I. E. Tolpygin
  • E. N. Shepelenko
  • Yu. V. Revinskii
  • A. D. Dubonosov
  • V. A. Bren
  • V. I. Minkin
Article

New derivatives of the benzo[de]isoquinoline-1,3-dione system containing an amino group were synthesized by the reaction of 2-benzyl-6-bromobenzo[de]isoquinoline-1,3-dione with ethylenediamine and hydrazine. Further functionalization of the free amino groups leads to imines, amines, thioureas, and hydrazones. Some compounds exhibit high chemosensor selectivity in the determination of anions.

Keywords

aminoethylamines azomethines benzo[de]isoquinoline-1,3-diones (1,8-naphthalimides) hydrazines hydrazones chemosensor activity fluorescence 

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Copyright information

© Springer Science+Business Media New York 2012

Authors and Affiliations

  • I. E. Tolpygin
    • 1
  • E. N. Shepelenko
    • 2
  • Yu. V. Revinskii
    • 2
  • A. D. Dubonosov
    • 2
  • V. A. Bren
    • 1
  • V. I. Minkin
    • 1
    • 2
  1. 1.Scientific-Research Institute of Physical and Organic ChemistrySouthern Federal UniversityRostov-on-the-DonRussia
  2. 2.Southern Scientific CenterRussian Academy of SciencesRostov-on-the-DonRussia

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