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Chromogenic and fluorogenic detection of selected anions by bis-terpyridine Fe(II) complex through displacement approach
This paper deals with synthesis, characterization and anion recognition properties of a homoleptic bis-terpyridine Fe(II) complex covalently coupled with diarylethene unit. The recognition event was examined in both organic as well as mixed aqueous–organic medium through different optical channels a...
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Published in: | Journal of chemical sciences (Bangalore, India) India), 2018-07, Vol.130 (7), p.1-11, Article 84 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | This paper deals with synthesis, characterization and anion recognition properties of a homoleptic bis-terpyridine Fe(II) complex covalently coupled with diarylethene unit. The recognition event was examined in both organic as well as mixed aqueous–organic medium through different optical channels and spectroscopic techniques by taking advantage of metal–ligand interaction in the complex. The complex acts as sensor for
F
-
,
OAc
-
and
CN
-
among the other studied anions (
F
-
,
Cl
-
,
Br
-
,
I
-
,
CN
-
,
OAc
-
,
H
2
PO
4
-
,
SCN
-
,
BF
4
-
and
ClO
4
-
)
without selectivity. In contrast to acetonitrile, the complex acts as highly selective chromogenic and fluorogenic sensor for only
CN
-
in water. Detection limit of the metalloreceptor towards
CN
-
was determined from the absorption and emission titration data and the observed values lie in the order of
10
-
9
M in acetonitrile and
10
-
8
M in mixed aqueous–organic media.
Graphical Abstract
SYNOPSIS
Anion sensing property of a bis-terpyridine Fe(II) complex was thoroughly investigated in both acetonitrile and water–acetonitrile (100:1, v/v) media through different optical channels and spectroscopic techniques. Interestingly, the complex acts as chromogenic and fluorogenic receptor for cyanide in predominantly aqueous medium with very low detection limit. |
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ISSN: | 0974-3626 0973-7103 |
DOI: | 10.1007/s12039-018-1484-6 |