Observing reduction of 4-nitrobenzenthiol on gold nanoparticlesin situ using surface-enhanced Raman spectroscopy

Literature Information

Publication Date 2013-06-18
DOI 10.1039/C3CP51385H
Impact Factor 3.676
Authors

Xiaoqian Ren, Tingting You, Li Jiang, Hongyan Zhang, Penggang Yin, Lin Guo


View Original

Abstract

In this article, reduction of 4-nitrobenzenthiol (4-NBT) on Au nanoparticles (NPs) was characterized using surface-enhanced Raman scattering (SERS). Plasmon-driven chemical transformation from 4-NBT dimering into p,p′-dimercaptoazobenzene (DMAB) has been investigated on the surface of Au NPs. The laser power-dependent SERS spectra of 4-NBT on the surface of Au substrates were studied, and show that the laser power has an influence on the SERS signals of 4-NBT on Au NPs and production of DMAB by a plasmon-driven surface-catalyzed chemical reaction tends to be much easier under relative high laser power. Furthermore, we have used simple and efficient Au substrates (gold NPs with a size around 45 nm) exhibiting both catalytic properties and SERS activities to monitor the catalytic reaction of surface catalytic reaction process with borohydride solution. The experiments prove that the nitro-to-amino group conversion could be completed by borohydride at ambient conditions on Au substrates. Illuminated with high laser power, 4-NBT molecules and already formed DMAB molecules are further reduced into 4-aminobenzenthiol (4-ABT) by the addition of borohydride, While with low laser power 4-NBT molecules are transformed into 4-ABT with DMAB as the intermediate, which proves Au NPs are a mild and promising catalyst. Our studies might be helpful in extending the understanding of chemical reactions of 4-NBT and related research as well as providing a new strategy synthesis of azo dyes and anilines.

Related Literature

Synthesis of clay-armored poly(vinylidene chloride-co-methyl acrylate) latexes by Pickering emulsion polymerization and their film-forming properties

Laura Delafresnaye, Pierre-Yves Dugas, Pierre-Emmanuel Dufils, Isabelle Chaduc, Jérôme Vinas, Muriel Lansalot, Elodie Bourgeat-Lami

2017-08-14 Paper

DOI: 10.1039/C7PY00902J

Chalcogenide hybrid inorganic/organic polymers (CHIPs) via inverse vulcanization and dynamic covalent polymerizations

Yueyan Zhang, Katrina M. Konopka, Richard S. Glass, Kookheon Char

2017-04-19 Paper

DOI: 10.1039/C7PY00587C

Retracted Article: A polyurethane–chitosan brush as an injectable hydrogel for controlled drug delivery and tissue engineering

Arun Kumar Mahanta, Sudipta Senapati, Pralay Maiti

2017-09-19 Paper

DOI: 10.1039/C7PY01218G

Photophysics and photochemistry of the EE and ZE isomers of 1-(n-pyridyl)-4-phenyl-1,3-butadiene (n = 2, 3 and 4)

G. Bartocci, G. Galiazzo, U. Mazzucato, A. Spalletti

2001-01-05 Paper

DOI: 10.1039/B009107N

Pulsed laser polymerisation studies of methyl methacrylate in the presence of AlCl3 and ZnCl2 – evidence of propagation catalysis

Jing Y. Jiang, Leesa M. Smith, Jason H. Tyrell, Michelle L. Coote

2017-09-06 Paper

DOI: 10.1039/C7PY01355H

Tunable intramolecular H-bonding promotes benzoic acid activity in polymerization: inspiration from nature

Jiaxi Xu, Kun Yang, Jingjing Liu, Herui Sun, Songquan Xu, Haixin Wang, Tianfo Guo, He Dong

2017-09-27 Paper

DOI: 10.1039/C7PY01451A

3D-Printed OFETs of the 1,4-bis(3-phenylquinoxalin-2-yl)benzene-based polymer semiconductors

Yuli Huang, Hua Chen, Junwei Yang, Wanli Tian, Weizhi Wang

2017-07-20 Paper

DOI: 10.1039/C7PY00810D

You might also like

Compound Q&A

Are there alternatives to 1-(4-Chlorophenyl)-N-hydroxymethanimine (CAS: 3848-36-0) in synthesis?

When considering alternatives to 1-(4-Chlorophenyl)-N-hydroxymethanimine (CAS: 3...

3848-36-01-(4-Chlorophenyl)-N...
Compound Q&A

How is 3-(4-Bromophenyl)-5-(2-fluorophenyl)-1,2,4-oxadiazole (CAS: 419553-16-5) typically synthesized?

3-(4-Bromophenyl)-5-(2-fluorophenyl)-1,2,4-oxadiazole is synthesized through a m...

419553-16-53-(4-Bromophenyl)-5-...
Compound Q&A

How is 5-Chloro-2-(4-chlorophenyl)-4-methyl-6-[3-(1-piperidinyl)propoxy]pyrimidine (CAS: 1639220-19-1) typically synthesized?

5-Chloro-2-(4-chlorophenyl)-4-methyl-6-[3-(1-piperidinyl)propoxy]pyrimidine (CAS...

1639220-19-15-Chloro-2-(4-chloro...
Compound Q&A

What industries use 2-Chloro-4-(difluoromethoxy)pyridine (CAS: 1206978-15-5)?

2-Chloro-4-(difluoromethoxy)pyridine is used in the pharmaceutical industry for ...

1206978-15-52-Chloro-4-(difluoro...
Compound Q&A

What regulatory guidelines apply to 3-Chloro-6-methylpyridazine (CAS: 1121-79-5)?

3-Chloro-6-methylpyridazine (CAS: 1121-79-5) is classified under the Globally Ha...

1121-79-53-Chloro-6-methylpyr...
Compound Q&A

Are there alternatives to Methyl 4,5-dimethyl-2-nitrobenzoate in synthesis?

Several alternatives can be used in the synthesis of Methyl 4,5-dimethyl-2-nitro...

90922-74-0Methyl 4,5-dimethyl-...
Compound Q&A

Are there alternatives to (2E,2'E)-3,3'-(1,4-Phenylene)bisacrylaldehyde in synthesis?

Alternatives to (2E,2'E)-3,3'-(1,4-Phenylene)bisacrylaldehyde include other acry...

63405-68-5(2E,2'E)-3,3'-(1,4-P...
Compound Q&A

What is 3-Amino-5-chloropyridin-2-ol hydrochloride (CAS: 1261906-29-9)?

3-Amino-5-chloropyridin-2-ol hydrochloride is an organic compound with the CAS n...

1261906-29-93-Amino-5-chloropyri...
Compound Q&A

What precautions should be taken when handling 6,7-Difluoro-2,3-dihydro-4H-chromen-4-one (CAS: 1092349-93-3)?

When handling 6,7-Difluoro-2,3-dihydro-4H-chromen-4-one, it is essential to wear...

1092349-93-36,7-Difluoro-2,3-dih...

Source Journal

Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
CiteScore: 5.5
Self-citation Rate: 10.3%
Articles per Year: 3036

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.

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.