NEW CHEMOSENSOR SYSTEMS OF THE BENZO[<i>de</i>]ISOQUINOLINE-1,3-DIONE SERIES

Authors

  • И. Е. Толпыгин Scientific-Research Institute of Physical and Organic Chemistry, Southern Federal University
  • Е. Н. Шепеленко Southern Scientific Center, Russian Academy of Sciences
  • Ю. В. Ревинский Southern Scientific Center, Russian Academy of Sciences
  • А. Д. Дубоносов Southern Scientific Center, Russian Academy of Sciences
  • В. А. Брень Scientific-Research Institute of Physical and Organic Chemistry, Southern Federal University
  • В. И. Минкин Scientific-Research Institute of Physical and Organic Chemistry, Southern Federal University; Southern Scientific Center, Russian Academy of Sciences

DOI:

https://doi.org/10.1007/934

Keywords:

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

Abstract

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.

Authors: I. E. Tolpygin, E. N. Shepelenko, Yu. V. Revinskii, A. D. Dubonosov, V. A. Bren, and V. I. Minkin

English Translation in Chemistry of Heterocyclic Compounds, 2012, 48 (9), pp 1325-1331

http://link.springer.com/article/10.1007/s10593-012-1140-x

Downloads

Published

2013-09-04

Issue

No. 9 (2012)

Section

Original Papers