Improving Copper(II) Sensitivity by Combined use of AIEE Active and Inactive Schiff Bases
An aggregation-induced emission enhancement (AIEE) active Schiff base PNN was synthesized by condensing benzidine with 2-hydroxynaphthaldehyde. The green-fluorescent PNN (λ em = 510 nm) in DMF turned to yellow-fluorescent PNN (λ em = 557 nm) upon increasing the fractions of HEPES buffer (10 mM, pH...
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Published in | Journal of fluorescence Vol. 34; no. 3; pp. 1065 - 1074 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
New York
Springer US
01.05.2024
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | An aggregation-induced emission enhancement (AIEE) active Schiff base PNN was synthesized by condensing benzidine with 2-hydroxynaphthaldehyde. The green-fluorescent PNN (λ
em
= 510 nm) in DMF turned to yellow-fluorescent PNN (λ
em
= 557 nm) upon increasing the fractions of HEPES buffer (10 mM, pH 7.4) above 40%. The DLS study supports the self-aggregation of PNN that restricts the intramolecular rotation and activates the excited-state intramolecular proton transfer (ESIPT) process. The fluorescence emission of AIEE active PNN was quenched by Cu
2+
with an estimated detection limit of 2.1 µM. Interestingly, the detection limit of PNN towards Cu
2+
was improved in the presence of an AIEE inactive Schiff base PBPM obtained by reacting 1,4-diaminobenzene with pyridine-4-carbaldehyde. The mixed PNN-PBPM showed a detection limit of 0.49 µM. The practical utility of PNN-PBPM was validated by quantifying Cu
2+
ions in real environmental water samples and green tea. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1053-0509 1573-4994 |
DOI: | 10.1007/s10895-023-03347-4 |