Hydrogenation of phenol to cyclohexanol using carbon encapsulated Ni–Co alloy nanoparticles

Literature Information

Publication Date 2021-12-07
DOI 10.1039/D1RE00457C
Impact Factor 4.239
Authors

Shuai Wang, Tianhan Zhu, Nan Jiang, Chunlei Zhang, Huan Wang, Yanguang Chen, Feng Li, Hua Song


View Original

Abstract

The preparation of cost-effective and highly active catalysts for hydrogenation of phenol to cyclohexanol remains a great challenge. Here, we develop a simple and controllable synthetic route to prepare non-precious bimetallic NiCo(x/y)@C–T catalysts (Ni/Co = x/y, T = pyrolysis temperature) from NiCo(x/y)–MOF-74 for hydrogenation of phenol with cyclohexanol as the only product under mild reaction conditions. The results showed that all the bimetallic catalysts performed much better than their corresponding monometallic catalysts because of the strong synergistic effect between Ni and Co. And NiCo(1/2)@C-600 exhibited the best performance with 100% phenol and 100% cyclohexanol selectivity at the reaction conditions of a temperature of 120 °C, a H2 pressure of 1.5 MPa and time of 2 h. Furthermore, this series of catalysts also displayed excellent recyclability. We believe that this MOF-templated strategy can provide a simple and repeatable route to synthesize high-performance hydrogenation catalysts.

Related Literature

Metal-free synthesis of fulleropyrrolidin-2-ols: a novel reaction of [60]fullerene with amines and 2,2-disubstituted acetaldehydes

Gang Huang, Meng Zhang, Hui-Juan Wang, Fa-Bao Li, Fei Yang, Li Liu, Chao-Yang Liu, Abdullah M. Asiri, Khalid A. Alamry

2018-09-27 Paper

DOI: 10.1039/C8OB01903G

First enantioselective total synthesis of altersolanol A

Bastian Mechsner

2018-10-01 Paper

DOI: 10.1039/C8OB02113A

Azodicarboxylate-free esterification with triphenylphosphine mediated by flavin and visible light: method development and stereoselectivity control

Michal März, Michal Kohout, Tomáš Neveselý, Josef Chudoba, Dorota Prukała, Stanislaw Niziński, Marek Sikorski, Gotard Burdziński, Radek Cibulka

2018-09-03 Paper

DOI: 10.1039/C8OB01822G

Catalytic asymmetric Henry reactions of silyl nitronates with aldehydes

Tine Risgaard, Kurt V. Gothelf, Karl Anker Jørgensen

2002-12-03 Paper

DOI: 10.1039/B208859M

UV light-driven asymmetric vinylogous aldol reaction of isatins with 2-alkylbenzophenones and enantioselective synthesis of 3-hydroxyoxindoles

Shixuan Cao, Jiatian Li, Taishan Yan, Jie Han

2021-12-07 Research Article

DOI: 10.1039/D1QO01555A

Contents list

Front/Back Matter

DOI: 10.1039/C8OB90138D

l-Dopa and dopamine conjugated naphthalenediimides modulate amyloid β toxicity

Madhu Ramesh, Pandeeswar Makam, Chandrashekhar Voshavar, Harshavardhan Khare, Kolla Rajasekhar, Suryanarayanarao Ramakumar, Thimmaiah Govindaraju

2018-09-28 Paper

DOI: 10.1039/C8OB01691G

Back cover

Cover

DOI: 10.1039/C8OB90144A

Dependence of selective enclathration on types of cholic acid crystals

Nungruethai Yoswathananont, Kazuki Sada, Mikiji Miyata, Shigendo Akita, Kazunori Nakano

2002-11-29 Paper

DOI: 10.1039/B210544F

Asymmetric fluorination of indanone-2-carboxylates using a polystyrene-supported diphenylamine-linked bis(oxazoline) complex

Biao Wang, Yifeng Wang, Yidong Jiang, Mingming Chu, Suosuo Qi, Wanzhen Ju, Danqian Xu

2018-09-28 Paper

DOI: 10.1039/C8OB01943F

You might also like

Compound Q&A

What is the market or research trend for N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0)?

N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0) is increasingly being used ...

52818-63-0N-(4-Methoxybenzyl)-...
Compound Q&A

What precautions should be taken when handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate (CAS: 1050507-06-6)?

When handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate, appropriate p...

1050507-06-6Ethyl 4-(2-chlorophe...
Compound Q&A

What regulatory guidelines apply to diethyldiselane (CAS: 628-39-7)?

Diethyldiselane (CAS: 628-39-7) is classified under the Globally Harmonized Syst...

628-39-7Diethyldiselane
Compound Q&A

What is the market or research trend for oxocopper (CAS: 12053-18-8)?

The market for oxocopper (CAS: 12053-18-8) is primarily driven by its use in cat...

12053-18-8oxocopper; oxo-(oxoc...
Compound Q&A

What is the market or research trend for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-carboxylic acid?

The market for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-c...

1268519-54-55-{[(2-Methyl-2-prop...
Compound Q&A

What is 2-(1-Pyrrolidinyl)-4-pyridinamine (CAS: 35981-63-6)?

2-(1-Pyrrolidinyl)-4-pyridinamine is a chemical compound with the CAS number 359...

35981-63-62-(1-Pyrrolidinyl)-4...
Compound Q&A

What are the physical and chemical properties of 2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1)?

2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1) is a crystalline sol...

91556-75-12-(3-Pyridinyl)-1-az...
Compound Q&A

How is (S)-Alpha-allyl-proline hydrochloride (CAS: 129704-91-2) typically synthesized?

(S)-Alpha-allyl-proline hydrochloride is usually synthesized via a Wittig reacti...

129704-91-2(S)-Alpha-allyl-prol...
Compound Q&A

What is 3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5)?

3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5) is an organic compound w...

4857-42-53-Methyl-1,2-oxazole...
Compound Q&A

How is Lys-SMCC-DM1 (CAS: 1281816-04-3) typically synthesized?

Lys-SMCC-DM1 is synthesized via a multi-step process involving the coupling of S...

1281816-04-3Lys-SMCC-DM1

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.