Selective synthesis of azoxybenzenes from nitrobenzenes by visible light irradiation under continuous flow conditions

Literature Information

Publication Date 2019-08-05
DOI 10.1039/C9RE00265K
Impact Factor 4.239
Authors

Yasuhiro Nishiyama, Akira Fujii, Hajime Mori


View Original

Abstract

Herein, we report a highly selective preparation method of azoxybenzenes from nitrobenzenes by visible-light irradiation. In a batch, this reaction method affords the corresponding aniline derivatives or intermediates (nitrosobenzene or phenyl hydroxylamine); however, in flow microreactors, azoxybenzenes are successfully obtained with very high selectivity.

Related Literature

The relevance of interfaces for oxide ion transport in yttria stabilized zirconia (YSZ) thin films

Matthias Gerstl, Gernot Friedbacher, Frank Kubel, Herbert Hutter, Jürgen Fleig

2012-11-20 Paper

DOI: 10.1039/C2CP42347B

Dual reaction channels for photocatalytic oxidation of phenylmethanol on anatase

Ye-Fei Li, Zhi-Pan Liu

2012-11-22 Communication

DOI: 10.1039/C2CP44137C

Visualization of clusters in polymer electrolyte membranes by electron microscopy

Sergey Yakovlev, Kenneth H. Downing

2012-11-01 Perspective

DOI: 10.1039/C2CP42969A

Unraveling the binding interaction and kinetics of a prospective anti-HIV drug with a model transport protein: results and challenges

Bijan Kumar Paul, Debarati Ray, Nikhil Guchhait

2012-11-21 Paper

DOI: 10.1039/C2CP42539D

Single-crystal adsorptioncalorimetry and density functional theory of CO chemisorption on fcc Co{110}

Kristine Liao, Vittorio Fiorin, David S. D. Gunn, Stephen J. Jenkins, David A. King

2013-02-13 Paper

DOI: 10.1039/C3CP43836H

Anchoring sites to the STM tip can explain multiple peaks in single molecule conductance histograms

S. Alexis Paz, Martin E. Zoloff Michoff, Christian F. A. Negre, Jimena A. Olmos-Asar, Marcelo M. Mariscal, Cristián G. Sánchez, Ezequiel P. M. Leiva

2012-11-22 Paper

DOI: 10.1039/C2CP43811A

Front cover

Cover

DOI: 10.1039/C3CP90018E

Formation of an electron hole doped film in the α-Fe2O3 photoanode upon electrochemical oxidation‡

Rita Toth, Michael Grätzel, Edwin C. Constable, Artur Braun

2012-10-09 Paper

DOI: 10.1039/C2CP42597A

You might also like

Compound Q&A

What is 3-Fluoro-2-methylbenzylamine (CAS: 771573-36-5)?

3-Fluoro-2-methylbenzylamine is an organic compound with the CAS number 771573-3...

771573-36-53-Fluoro-2-methylben...
Compound Q&A

Is Tert-butyl 2-(oxetan-3-ylidene)acetate (CAS: 1207175-03-8) safe?

Tert-butyl 2-(oxetan-3-ylidene)acetate is considered safe for its intended uses ...

1207175-03-8Tert-butyl 2-(oxetan...
Compound Q&A

What precautions should be taken when handling 4-Acetyl-2-fluorobenzonitrile (CAS: 214760-18-6)?

Proper personal protective equipment (PPE) such as gloves, goggles, and a lab co...

214760-18-64-Acetyl-2-fluoroben...
Compound Q&A

How is 2-Ethyl-4-methyl-1,3-thiazole (CAS: 15679-12-6) typically synthesized?

2-Ethyl-4-methyl-1,3-thiazole is commonly synthesized via the reaction of thiour...

15679-12-62-Ethyl-4-methyl-1,3...
Compound Q&A

How should 5',5''-([2,2'-Bithiophene]-5,5'-diyl)bis(([1,1':3',1''-terphenyl]-4,4''-dicarboxylic acid)) (CAS: 1227780-71-3) be stored?

This compound should be stored in a cool, dry place away from direct sunlight an...

1227780-71-35',5''''-([2,2'-Bith...
Compound Q&A

What regulatory guidelines apply to L-Lysine Acetate Salt (CAS: 52315-92-1)?

L-Lysine Acetate Salt (CAS: 52315-92-1) is subject to various regulatory guideli...

52315-92-1L-LYSINE ACETATE SAL...
Compound Q&A

Is 6-Fluoro-3-hydroxy-2-pyrazinecarboxamide (CAS: 259793-96-9) safe?

6-Fluoro-3-hydroxy-2-pyrazinecarboxamide (CAS: 259793-96-9) is generally conside...

259793-96-96-Fluoro-3-hydroxy-2...
Compound Q&A

What are the physical and chemical properties of 1,1'-Sulfonylbis(1H-imidazole) (CAS: 7189-69-7)?

1,1'-Sulfonylbis(1H-imidazole) is a crystalline solid with a molecular weight of...

7189-69-71,1'-Sulfonylbis(1H-...
Compound Q&A

What industries use 4-methyl-7-nitro-1H-indole-3-carbonitrile (CAS: 289483-82-5)?

4-Methyl-7-nitro-1H-indole-3-carbonitrile (CAS: 289483-82-5) is primarily used i...

289483-82-54-methyl-7-nitro-1H-...
Compound Q&A

How should waste containing 5-Bromo-3-indolyl-beta-galactoside (CAS: 97753-82-7) be handled?

Waste containing 5-Bromo-3-indolyl-beta-galactoside (CAS: 97753-82-7) should be ...

97753-82-75-Bromo-3-indolyl-be...

Source Journal

Reaction Chemistry & Engineering

Reaction Chemistry & Engineering
CiteScore: 0
Self-citation Rate: 8.8%
Articles per Year: 284

Reaction Chemistry & Engineering is an interdisciplinary journal reporting cutting-edge research focused on enhancing the understanding and efficiency of reactions. Reaction engineering leverages the interface where fundamental molecular chemistry meets chemical engineering and technology. Challenges in chemistry can be overcome by the application of new technologies, while engineers may find improved solutions for process development from the latest developments in reaction chemistry. Reaction Chemistry & Engineering is a unique forum for researchers whose interests span the broad areas of chemical engineering and chemical sciences to come together in solving problems of importance to wider society. All papers should be written to be approachable by readers across the engineering and chemical sciences. Papers that consider multiple scales, from the laboratory up to and including plant scale, are particularly encouraged.

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.