A hybrid of carbon dots with 4-chloro-7-nitro-2,1,3-benzoxadiazole for selective detection of p-phenylenediamine
The nucleophilic substitution reaction between 4-chloro-7-nitro-2,1,3-benzoxadiazole (NBD-Cl) and –NH 2 groups on amino-functionalized carbon dots (CDs) produces a novel carbon dot-based hybrid, CDs@NBD for short. In addition to the characteristic fluorescence emission of carbon dots at λ ex / λ em...
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Published in | Environmental science. Nano Vol. 4; no. 5; pp. 1037 - 1044 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
01.05.2017
|
Online Access | Get full text |
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Summary: | The nucleophilic substitution reaction between 4-chloro-7-nitro-2,1,3-benzoxadiazole (NBD-Cl) and –NH
2
groups on amino-functionalized carbon dots (CDs) produces a novel carbon dot-based hybrid, CDs@NBD for short. In addition to the characteristic fluorescence emission of carbon dots at
λ
ex
/
λ
em
= 360/443 nm, the CDs@NBD hybrid gives rise to new photoluminescence at
λ
ex
/
λ
em
= 460/544 nm, which is significantly quenched by
p
-phenylenediamine (PPD)
via
static quenching. This provides a novel sensing approach for fluorometric detection of PPD with CDs@NBD as a probe. A linear calibration graph is obtained within two concentration ranges of 0.1–1.0 μmol L
−1
and 1.0–10.0 μmol L
−1
, along with a detection limit of 56 nmol L
−1
and a RSD of <3% (at 1.0 μmol L
−1
). The common coexisting species in environmental and biological sample matrices cause no obvious interferences on the detection of PPD. The colour change of the CDs@NBD hybrid solution with the variation in PPD concentration also facilitates visual detection of PPD, which further demonstrates promising applications in environmental and biological sample analysis. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2051-8153 2051-8161 |
DOI: | 10.1039/C7EN00027H |