Selective dual detection of Hg2+ and TATP based on amphiphilic conjugated polythiophene-quantum dot hybrid materials

Literature Information

Publication Date 2021-03-02
DOI 10.1039/D1AN00166C
Impact Factor 4.616
Authors

Salah M. Tawfik, Ali A. Abd-Elaal, Yong-Ill Lee


View Original

Abstract

The design of multifunctional sensors based on biocompatible hybrid materials consisting of conjugated polythiophene-quantum dots for multiple environmental pollutants is a promising strategy for the development of new monitoring technologies. Herein, we present a new approach for the “on–off–on” sensing of Hg2+ and triacetone triperoxide (TATP) based on amphiphilic polythiophene-coated CdTe QDs (PQDs, PLQY ∼78%). The emission of the PQDs is quenched by Hg2+ ions via electron transfer interactions. Based on the strong interaction between TATP and Hg2+ ions, the addition of TATP to the PQD-Hg2+ complex results in a remarkable recovery of the PQD emission. Under the optimized conditions, the PQD sensor shows a good linear response to Hg2+ and TATP with detection limits of 7.4 nM and 0.055 mg L−1, respectively. Furthermore, the “on–off–on” sensor demonstrates good biocompatibility, high stability, and excellent selectivity in the presence of other metal ions and common explosives. Importantly, the proposed method can be used to determine the level of Hg2+ and TATP in environmental water samples.

Related Literature

A cationic 24-MC-8 manganese cluster with ring metals possessing three oxidation states [MnII4MnIII6MnIV2(μ4-O)2(μ3-O)4(μ3-OH)4(μ3-OCH3)2(pko)12](OH)(ClO4)3‡

Catherine Dendrinou-Samara, Curtis M. Zaleski, Andri Evagorou, Jeff W. Kampf, Vincent L. Pecoraro, Dimitris P. Kessissoglou

2003-09-30 Communication

DOI: 10.1039/B309439A

Selective deposition of polystyrene nanoparticles in a nanoetchpit array on a silicon substrate

Manabu Tanaka, Takumi Hosaka, Takashi Tanii, Iwao Ohdomari, Hiroyuki Nishide

2004-03-16 Communication

DOI: 10.1039/B315816K

Linear antiferromagnetism in Ba2CoS3

A. Maignan

2004-02-27 Communication

DOI: 10.1039/B400084F

Medium ring synthesis by radical ipso-substitution

David C. Harrowven, Nathalie L'Helias, Jonathan D. Moseley, Nigel J. Blumire, Stuart R. Flanagan

2003-10-01 Communication

DOI: 10.1039/B309496K

Molecular recognition. Self-assembly of molecular trigonal prisms and their host–guest adducts

James D. Crowley, Andrew J. Goshe, Brice Bosnich

2003-10-17 Communication

DOI: 10.1039/B307385H

Supported choline hydroxide (ionic liquid) as heterogeneous catalyst for aldol condensation reactions

Sònia Abelló, Francisco Medina, Xavier Rodríguez, Yolanda Cesteros, Pilar Salagre, Jesús E. Sueiras, Didier Tichit, Bernard Coq

2004-04-01 Communication

DOI: 10.1039/B401448K

Heteropoly acid as a novel nitrene transfer agent: a facile and practical aziridination of olefins with Chloramine-T

G. D. Kishore Kumar, Sundarababu Baskaran

2004-03-23 Communication

DOI: 10.1039/B402371D

Carbonate and oxalate dianions as prolific hydrogen-bond acceptors in supramolecular assembly‡

Chi-Keung Lam, Thomas C. W. Mak

2003-10-08 Communication

DOI: 10.1039/B306649E

Room temperature borylation of arenes and heteroarenes using stoichiometric amounts of pinacolborane catalyzed by iridium complexes in an inert solvent

Tatsuo Ishiyama, Yusuke Nobuta, John F. Hartwig, Norio Miyaura

2003-10-22 Communication

DOI: 10.1039/B311103B

You might also like

Compound Q&A

What is the market or research trend for N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0)?

N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0) is increasingly being used ...

52818-63-0N-(4-Methoxybenzyl)-...
Compound Q&A

What precautions should be taken when handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate (CAS: 1050507-06-6)?

When handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate, appropriate p...

1050507-06-6Ethyl 4-(2-chlorophe...
Compound Q&A

What regulatory guidelines apply to diethyldiselane (CAS: 628-39-7)?

Diethyldiselane (CAS: 628-39-7) is classified under the Globally Harmonized Syst...

628-39-7Diethyldiselane
Compound Q&A

What is the market or research trend for oxocopper (CAS: 12053-18-8)?

The market for oxocopper (CAS: 12053-18-8) is primarily driven by its use in cat...

12053-18-8oxocopper; oxo-(oxoc...
Compound Q&A

What is the market or research trend for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-carboxylic acid?

The market for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-c...

1268519-54-55-{[(2-Methyl-2-prop...
Compound Q&A

What is 2-(1-Pyrrolidinyl)-4-pyridinamine (CAS: 35981-63-6)?

2-(1-Pyrrolidinyl)-4-pyridinamine is a chemical compound with the CAS number 359...

35981-63-62-(1-Pyrrolidinyl)-4...
Compound Q&A

What are the physical and chemical properties of 2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1)?

2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1) is a crystalline sol...

91556-75-12-(3-Pyridinyl)-1-az...
Compound Q&A

How is (S)-Alpha-allyl-proline hydrochloride (CAS: 129704-91-2) typically synthesized?

(S)-Alpha-allyl-proline hydrochloride is usually synthesized via a Wittig reacti...

129704-91-2(S)-Alpha-allyl-prol...
Compound Q&A

What is 3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5)?

3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5) is an organic compound w...

4857-42-53-Methyl-1,2-oxazole...
Compound Q&A

How is Lys-SMCC-DM1 (CAS: 1281816-04-3) typically synthesized?

Lys-SMCC-DM1 is synthesized via a multi-step process involving the coupling of S...

1281816-04-3Lys-SMCC-DM1

Source Journal

Analyst

Analyst
CiteScore: 7.8
Self-citation Rate: 5.6%
Articles per Year: 653

Analyst publishes analytical and bioanalytical research that reports premier fundamental discoveries and inventions, and the applications of those discoveries, unconfined by traditional discipline barriers.

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.