Add like
Add dislike
Add to saved papers

Ru nanoparticles supported on nitrogen-doped porous carbon derived from ZIF-8 as an efficient catalyst for the selective hydrogenation of p-chloronitrobenzene and p-bromonitrobenzene.

Ruthenium (Ru) nanoparticles (NPs) are supported on nitrogen-doped porous carbon (NPC) derived from metal-organic-framework (MOF) ZIF-8 for the first time. NPC is prepared by the direct carbonization of ZIF-8 crystals, which not only retains the original morphology of ZIF-8 but also provides a high surface area and stable chemical-physical properties. Ru NPs were supported by different methods. Four types of Ru-based catalysts are tested in the selective hydrogenation of p-chloronitrobenzene (p-CNB) and p-bromonitrobenzene (p-BNB) to haloanilines. Different catalytic activities and selectivities are obtained through these catalysts. After the screening of the catalysts and reaction conditions, high conversion and selectivity were obtained. The hydrogen pressure is limited to 1.5 MPa, which is much lower than most previous reports, and the dehalogenation reaction is restricted to a very low level. Furthermore, the dehalogenation properties of the Ru/NPC catalysts are also studied.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

Related Resources

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app