Rhodamine based turn-on chemosensor for Fe3+ in aqueous medium and interactions of its Fe3+ complex with DNA
A novel di-coordinating rhodamine-based chemosensor, HL with NO donor atoms, selectively and rapidly recognizes Fe3+ in the presence of all biologically relevant as well as toxic metal ions and numerous anions and also with other reactive oxygen and nitrogen species. It exhibits a lower detection li...
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Published in | New journal of chemistry Vol. 42; no. 5; pp. 3435 - 3443 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
CAMBRIDGE
Royal Soc Chemistry
07.03.2018
Royal Society of Chemistry |
Subjects | |
Online Access | Get full text |
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Summary: | A novel di-coordinating rhodamine-based chemosensor, HL with NO donor atoms, selectively and rapidly recognizes Fe3+ in the presence of all biologically relevant as well as toxic metal ions and numerous anions and also with other reactive oxygen and nitrogen species. It exhibits a lower detection limit (0.17 M) and comparatively higher formation constant (K-f = 1.72 x 10(4) M-1). The DNA-binding properties of [LFe(NO3)(2)](+) complex have been comprehensively studied by using UV-Vis, fluorescence, and optical melting studies and circular dichroism, which clearly indicate that [LFe(NO3)(2)](+) interacts with DNA via a groove binding mode. In particular, competition experiments with Hoechst and DAPI constitute firm evidence for this binding mode, and clearly rule out intercalation. The negative G(0) and positive S-0 values obtained from a calorimetric technique confirm the spontaneity of the binding of [LFe(NO3)(2)](+) with DNA. The resulting [LFe(NO3)(2)](+)/DNA composite material could be a valuable candidate for future photonics and/or biological applications. |
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ISSN: | 1144-0546 1369-9261 |
DOI: | 10.1039/c7nj04505k |