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Green Chemistry
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Journal Name
COMMUNICATION
DOI: 10.1039/D0GC00633E
Benignity and Efficient Resource Utilization, and National
Department of Education Engineering Research Centre for
Chemical Process Simulation and Optimization.
amino groups combine with different kinds of naphthalene free
radicals to form corresponding naphthylamine and other oxidative
products. Affected by steric hindrance, the heterocyclic activation
and homocyclic passivate effector by the protonated amino radical
+
ion (-NH3 ), the formations of 1-naphthylamine and 1,5-
diaminonaphthalene are relatively easier than other positions of
naphthalene ring. It can also explain why there are few amounts of
2,3-diaminonaphthalene and 1,8-diaminonaphthalene formed
Notes and references
during the reaction.
Additionally, considered the control
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Conflicts of interest
There are no conflicts to declare.
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Acknowledgments
This work was supported by NSFC (21908185), Project of
Hunan Provincial Natural Science Foundation of China
(2016JJ2123, 2018JJ3497), Project of Hunan Provincial
This journal is © The Royal Society of Chemistry 20xx
J. Name., 2013, 00, 1-3 | 5
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