Electrogenerated chemiluminescence at a 9,10-diphenylanthracene/polyvinyl butyral film modified electrode with a tetraphenylborate coreactant

Literature Information

Publication Date 2018-06-08
DOI 10.1039/C8AN00889B
Impact Factor 4.616
Authors

Guobao Xu


View Original

Abstract

A new, efficient electrochemiluminescent (ECL) system based on a 9,10-diphenylanthracene/polyvinyl butyral film modified glassy carbon electrode and a tetraphenylborate anion coreactant is described. The system demonstrates strong dependence of its response on the potential scan rate. In pulsed excitation mode, the system allows for tetraphenylborate detection at a level down to 5 nM with a broad range of linear responses. The anodic cyclic voltammetry response of the system shows 2 distinct ECL waves. It was found that the first of them is due to the reaction of an oxidized fluorophore with tetraphenylborate while the second one is due to the oxidation of tetraphenylborate only. The presented results demonstrate the high potential of the tetraphenylborate coreactant for exciting pulsed ECL in fluorescent species/labels immobilized on the electrode surface, which has application potential for a number of existing ECL assay systems. Due to the ability of tetraphenylborate ions to interact with a number of cations and inorganic oxidants, the developed ECL system can also be applied for quantification based on ECL quenching that was demonstrated on the examples of hydrogen peroxide and hypochlorite.

Related Literature

Back cover

Cover

DOI: 10.1039/D0CP90073G

Structural relationships for the design of responsive azobenzene-based lyotropic liquid crystals

Luke W. Giles, Joshua B. Marlow, Calum S. G. Butler, Geosmin A. Turpin, Liliana de Campo, Stephen T. Mudie, Charl F. J. Faul, Rico F. Tabor

2020-01-30 Paper

DOI: 10.1039/C9CP05463D

Theoretical study on the stability and aromaticity in silapentafulvenes towards triplet ground state species

Jiashun Wu, Alvi Muhammad Rouf, Yuanyuan Huang, Danling Zhuang, Jun Zhu

2020-02-03 Paper

DOI: 10.1039/C9CP06506G

Energy landscape of Au13: a global view of structure transformation

Xiao-Tian Li, Shao-Gang Xu

2020-01-27 Paper

DOI: 10.1039/C9CP06463J

On the microscopic origin of the cryoprotective effect in lysine solutions

Guadalupe N. Ruiz, Nicola Steinke, Silvina Cerveny, Roberto Macovez, Elvira Guàrdia, Sebastian Busch, Sylvia E. McLain, Christian D. Lorenz, Luis Carlos Pardo

2020-03-06 Paper

DOI: 10.1039/C9CP06192D

Excited state hydrogen transfer dynamics in phenol–(NH3)2 studied by picosecond UV-near IR-UV time-resolved spectroscopy

Shun-ichi Ishiuchi, Junko Kamizori, Norihiro Tsuji, Makoto Sakai, Mitsuhiko Miyazaki, Claude Dedonder

2020-02-10 Paper

DOI: 10.1039/C9CP06369B

Electronic structure, doping effect and topological signature in realistic intermetallics Li3−xNaxM (x = 3, 2, 1, 0; M = N, P, As, Sb, Bi)

Lei Jin, Xiaoming Zhang, Tingli He, Weizhen Meng, Xuefang Dai, Guodong Liu

2020-02-28 Paper

DOI: 10.1039/C9CP06033B

Synchrotron-based Mössbauer spectroscopy characterization of sublimated spin crossover molecules

Alberto Cini, Lorenzo Poggini, Alexander I. Chumakov, Rudolf Rüffer, Gabriele Spina, Alain Wattiaux, Mathieu Duttine, Mathieu Gonidec, Maria Fittipaldi, Patrick Rosa, Matteo Mannini

2020-02-26 Paper

DOI: 10.1039/C9CP04464G

Real-time degradation dynamics of hydrated per- and polyfluoroalkyl substances (PFASs) in the presence of excess electrons

Sharma S. R. K. C. Yamijala, Ravindra Shinde, Bryan M. Wong

2020-01-22 Communication

DOI: 10.1039/C9CP06797C

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 Compounds

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.