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Naphthyl hydrazone anchored with nitrosalicyl moiety as fluorogenic and chromogenic receptor for heavy metals (Ag+, Hg2+) and biologically important F− ion and its live cell imaging applications in HeLa cells and Zebrafish embryos.

Authors :
Krishnaveni, Karuppiah
Iniya, Murugan
Siva, Ayyanar
Vidhyalakshmi, Narayanadoss
Sasikumar, Sundaresan
Pandian Ramesh, Uthanda Kalai
Murugesan, Sepperumal
Source :
Journal of Molecular Structure. Oct2020, Vol. 1217, pN.PAG-N.PAG. 1p.
Publication Year :
2020

Abstract

A new naphthyl hydrazone anchored nitrosalicyl unit has been developed as a host for the selective and sensitive detection of Ag+, Hg2+ and F− ions in DMSO/water (9:1) medium. An obvious fluorescence enhancement was observed towards Ag+, Hg2+ and F− ions due to the inhibition of both photoinduced electron transfer (PET) process and C N isomerization phenomenon. Moreover, the binding stoichiometry of probe with Ag+, Hg2+ and F− ions was established based on Job's plot, 1H NMR, 19F NMR titrations and ESI-MS analysis. Furthermore, the sensing behavior of probe for Ag+, Hg2+ and F− ions was supported by Density Functional Theory (DFT) calculations. Besides, cell viability of the probe was demonstrated using live cell imaging experiment and the probe is proved to be an excellent chemical tool for mapping F− and Ag+ ions distribution in HeLa cells and Zebrafish embryos respectively in biological environments. • We reported a new naphthyl hydrazone anchored salicyl unit for the detection of Ag+/Hg2+/F− ions in DMSO/H 2 O (9:1 v/v) medium. • The binding ratio of ghost/guest was confirmed by Job's plot, 1H NMR titration, 19F NMR and ESI-MS analysis. • The probe has followed the inhibition of both PET and C N isomerization mechanistic pathway for sensing analytes. • The sensing mechanism was supported by DFT calculations. • The cell viability of the probe was demonstrated via live cell imaging experiments. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00222860
Volume :
1217
Database :
Academic Search Index
Journal :
Journal of Molecular Structure
Publication Type :
Academic Journal
Accession number :
143780302
Full Text :
https://doi.org/10.1016/j.molstruc.2020.128446