Luminescent MOFs for selective sensing of Ag and other ions (Fe() and Cr()) in aqueous solution
Two new title MOFs, [Zn(BTA) 2 ] n ( LMOF- 1 ) and [Zn 3 (BTA) 2 (5-tbuip) 2 ] n ( LMOF- 2 ) (BTA = 1 H -benzotriazole, 5-tbuip = 5- tert -butylisophthalic acid), have been synthesized by a solvothermal method. The structures of the two complexes have been determined by single-crystal X-ray diffract...
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Veröffentlicht in: | CrystEngComm 2022-03, Vol.24 (13), p.2479-2484 |
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Zusammenfassung: | Two new title MOFs, [Zn(BTA)
2
]
n
(
LMOF-
1
) and [Zn
3
(BTA)
2
(5-tbuip)
2
]
n
(
LMOF-
2
) (BTA = 1
H
-benzotriazole, 5-tbuip = 5-
tert
-butylisophthalic acid), have been synthesized by a solvothermal method. The structures of the two complexes have been determined by single-crystal X-ray diffraction analysis and further characterized by elemental analysis, IR spectroscopy, powder X-ray diffraction (PXRD) and thermogravimetric (TG) analysis. And the calculation of PLATON displays that the porosity values are 15.04% and 18.77%. Fluorescence analysis reveals that the two MOFs generate strong blue luminescence;
LMOF-
1
and
LMOF-
2
can be regarded as multiresponsive fluorescence sensors for Fe(
iii
) and Cr(
vi
) (CrO
4
2−
/Cr
2
O
7
2−
ions) detection with high sensitivity and selectivity and a low detection limit in water
via
fluorescence quenching. It is worth noting that most LMOFs for detecting Ag
+
to date are mainly formed with rare earth lanthanide metals, while there are still few Zn-based LMOF probes used in Ag
+
detection.
LMOF-
1
can detect trace Ag
+
in water with a low detection limit. In addition,
LMOF-
1
has excellent water stability and thermal stability, and is an excellent material for detecting Ag
+
in daily water samples.
Two metal-organic frameworks, [Zn(BTA)
2
]
n
(
LMOF-
1
), [Zn
3
(BTA)
2
(5-tbuip)
2
]
n
(
LMOF-
2
) (BTA = 1
H
-benzotriazole, 5-tbuip = 5-
tert
-butylisophthalic acid) have been solvothermally synthesized. They show strong blue luminescence and
LMOF-
1
shows unusually detecting behavior to Ag
+
. |
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ISSN: | 1466-8033 1466-8033 |
DOI: | 10.1039/d2ce00057a |