Catalysis in C−H and C−C Bond Activation

A special issue of Catalysts (ISSN 2073-4344). This special issue belongs to the section "Catalysis in Organic and Polymer Chemistry".

Deadline for manuscript submissions: 31 August 2026 | Viewed by 2113

Special Issue Editors


E-Mail Website
Guest Editor
School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing 100081, China
Interests: heterogeneous catalysis; catalyst design; process intensification; structure-activity relationships; alkane conversion; reaction mechanism and kinetics

E-Mail Website
Guest Editor Assistant
State Key Laboratory of Heavy Oil Processing, China University of Petroleum (Beijing), Beijing 102249, China
Interests: heterogeneous catalysis; CO2 hydrogenation; selective oxidation; catalyst dynamics

E-Mail Website
Guest Editor Assistant
Leibniz Institute for Catalysis (LIKAT), Albert-Einstein-Str. 29a, 18059 Rostock, Germany
Interests: heterogeneous catalysis; alkane dehydrogenation; olefin metathesis; zeolite

Special Issue Information

Dear Colleagues,

The efficient and selective activation of C−H and C−C bonds is a challenging yet crucial aspect for enhancing the formation of target products in catalysis, and has attracted widespread attention. Over the past few decades, some important catalytic processes such as dehydrogenation, catalytic cracking, aromatization, and oxygenation have been rapidly developed, and the study of C−H and C−C bond activation and its catalyst design during the above processes has been a hot research topic.

Considering the importance and increasing attention on this topic, this Special Issue of Catalysts, entitled “Catalysis in C−H and C−C Bond Activation”, explores cutting-edge advances in the design of catalytic systems for these challenging transformations, and covers the recent advancements in heterogeneous catalysis, homogeneous catalysis, organic synthesis, and enzyme catalysis. The Guest Editors encourage submissions in the following areas:

  • The development of catalysts for efficient C−H and C−C bond activation;
  • Mechanistic insights into C−H and C−C bond activation;
  • Computational and machine-learning-guided catalyst design;
  • Industrial applications and process optimization.

If you would like to submit papers for publication in this Special Issue or have any questions, please contact the in-house Editor, Ms. Georgie Guan (georgie.guan@mdpi.com).

Dr. Yaoyuan Zhang
Guest Editor

Dr. Qingxin Yang
Dr. Qiyang Zhang
Guest Editor Assistants

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 250 words) can be sent to the Editorial Office for assessment.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Catalysts is an international peer-reviewed open access monthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2200 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • catalyst design
  • catalytic mechanism
  • C−H bond activation
  • C−C bond activation
  • structure–activity relationships
  • catalytic processes

Benefits of Publishing in a Special Issue

  • Ease of navigation: Grouping papers by topic helps scholars navigate broad scope journals more efficiently.
  • Greater discoverability: Special Issues support the reach and impact of scientific research. Articles in Special Issues are more discoverable and cited more frequently.
  • Expansion of research network: Special Issues facilitate connections among authors, fostering scientific collaborations.
  • External promotion: Articles in Special Issues are often promoted through the journal's social media, increasing their visibility.
  • Reprint: MDPI Books provides the opportunity to republish successful Special Issues in book format, both online and in print.

Further information on MDPI's Special Issue policies can be found here.

Published Papers (1 paper)

Order results
Result details
Select all
Export citation of selected articles as:

Research

16 pages, 3295 KB  
Article
Insight into the Au/CoAlOx Catalyst with Spinel Structure for Efficient Oxidation of Benzyl Alcohol
by Meihui Bao, Sen Zhang, Wenhao Yang, Hao Liu, Shaojie Li, Jingjie Luo and Changhai Liang
Catalysts 2025, 15(11), 1053; https://doi.org/10.3390/catal15111053 - 4 Nov 2025
Cited by 1 | Viewed by 893
Abstract
Selective oxidation of benzyl alcohol to benzaldehyde is crucial for sustainable chemical synthesis, which provides the atom-economical and environmentally benign pathways. In this work, we used the in situ reduction immobilization to synthesize a series of Au nanoparticles supported by CoAlOx support [...] Read more.
Selective oxidation of benzyl alcohol to benzaldehyde is crucial for sustainable chemical synthesis, which provides the atom-economical and environmentally benign pathways. In this work, we used the in situ reduction immobilization to synthesize a series of Au nanoparticles supported by CoAlOx support with spinel structure for alkali-free oxidation of benzyl alcohol. The synthesis methodology was preliminarily optimized and the influence of Co/Al molar ratio in Au/CoAlOx on the catalytic performances was subsequently revealed based on characterizations. Results suggested that the electronic interaction between Au and CoAlOx can be regulated and maximized under the Co/Al ratio of 3. It became a main factor to modulate the dispersion of Au nanoparticles, surface chemical composition, as well as the oxygen adsorption/activation ability. Benefiting from such synergistic interaction, the optimized Au/Co3AlOx catalyst achieved 86.1% BnOH conversion under 99.9% benzaldehyde selectivity with well-maintained structural stability under recycle tests. This work provides a rational design strategy for developing highly efficient gold catalysts with well-constructed Au-support interfaces for the alkali-free oxidation of alcohol. Full article
(This article belongs to the Special Issue Catalysis in C−H and C−C Bond Activation)
Show Figures

Figure 1

Back to TopTop