Issue 38, 2021

Nitrogen-centered radical reaction leading to energetic materials: a mild and efficient access to N–N bridged compounds

Abstract

A radical reaction is a type of highly efficient organic reaction with a broad coverage in organic synthesis. However, its potential in the preparation of energetic materials is grossly underexplored. Now a novel nitrogen-centered radical reaction was discovered which features an N–N coupling capability, able to couple a pyrazole-based energetic compound to its N–N bridged dimer. The reaction exhibits high efficiency, while maintaining the traits of being mild, green, and facile without assistance from metal catalysis, photolysis, electrolysis or pyrolysis. The radical reaction mechanism was verified by a radical scavenger experiment and electron spin resonance spectroscopy.

Graphical abstract: Nitrogen-centered radical reaction leading to energetic materials: a mild and efficient access to N–N bridged compounds

Supplementary files

Article information

Article type
Communication
Submitted
06 Aug 2021
Accepted
10 Sep 2021
First published
10 Sep 2021

J. Mater. Chem. A, 2021,9, 21685-21688

Nitrogen-centered radical reaction leading to energetic materials: a mild and efficient access to N–N bridged compounds

Z. Zeng, Y. Liu, G. Cheng, W. Huang, H. Wei, J. M. Shreeve and Y. Tang, J. Mater. Chem. A, 2021, 9, 21685 DOI: 10.1039/D1TA06659E

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements