Feature Review Papers on Catalysis in Organic and Polymer Chemistry

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: 5 June 2026 | Viewed by 2179

Special Issue Editors


E-Mail Website1 Website2
Guest Editor
Schulich Faculty of Chemistry, Technion-Israel Institute of Technology, Haifa 3200008, Israel
Interests: actinide and lanthanide organometallic chemistry; polymerization catalysis; organo-f-complexes in catalysis; small molecule activation; transition metal organometallic chemistry; metal-ligand multiple bonding; group 4 organometallics in catalysis
Special Issues, Collections and Topics in MDPI journals

E-Mail Website
Guest Editor
State Key Laboratory of Advanced Fiber Materials, College of Materials Science and Engineering, Donghua University, Shanghai 201620, China
Interests: polymer chemistry; controllable coordination polymerization; metallocene catalysis; late transition metal catalysis; heterogeneous polymerization catalysis; high-performance polyolefin; functionalized polymer fiber
Special Issues, Collections and Topics in MDPI journals

E-Mail Website
Guest Editor Assistant
State Key Laboratory of Advanced Fiber Materials, College of Materials Science and Engineering, Donghua University, Shanghai 201620, China
Interests: organometallic catalysis; coordination polymerization catalysis; early and late transition metal catalysts; polar functionalized polyolefin; multifunctional polyolefin elastomer

Special Issue Information

Dear Colleagues,

We are excited to announce the launch of the Special Issue titled “Feature Review Papers on Catalysis in Organic and Polymer Chemistry”. This Special Issue aims to gather comprehensive and insightful review papers that focus on the latest advancements, challenges, and future directions in the field of catalysis in organic and polymer chemistry.

We welcome submissions that cover a wide range of topics, including, but not limited to, catalytic organic transformations for the synthesis of fine chemicals and polymers, green and sustainable catalytic reactions, precision polymerization, and the synthesis and reaction chemistry of new transition metal complexes for both organic transformations. Additionally, we are keen to receive contributions that explore mechanistic studies at the molecular level, such as kinetics, spectroscopic analysis, computational modeling, and reaction chemistry. Through this Special Issue, we aspire to create a valuable resource where researchers can exchange ideas, share their expertise, and foster further progress in this crucial and dynamic field of chemistry.

We look forward to receiving your contributions. 

Prof. Dr. Moris S. Eisen
Prof. Dr. Zhengguo Cai
Guest Editors

Dr. Mingyuan Li
Guest Editor Assistant

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

  • homogeneous catalysis
  • heterogeneous catalysis
  • organocatalysis
  • biocatalysis
  • fine chemicals synthesis
  • polymerization
  • asymmetric synthesis
  • mechanistic studies

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 (3 papers)

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

Review

34 pages, 6450 KB  
Review
Recent Progress in Palladium-Catalyzed Quinoline Formation: Synthetic Applications and Mechanistic Insights
by Nuno Viduedo, Luís Fernandes, Leonardo Pirvu and M. Manuel B. Marques
Catalysts 2026, 16(2), 134; https://doi.org/10.3390/catal16020134 - 1 Feb 2026
Viewed by 113
Abstract
Quinolines are key heterocyclic motifs with broad utility in pharmaceuticals, agrochemicals, and materials science. The development of efficient and sustainable synthetic routes to access structurally diverse quinolines remains an important goal in organic chemistry. This review focuses on the recent advances in palladium-catalyzed [...] Read more.
Quinolines are key heterocyclic motifs with broad utility in pharmaceuticals, agrochemicals, and materials science. The development of efficient and sustainable synthetic routes to access structurally diverse quinolines remains an important goal in organic chemistry. This review focuses on the recent advances in palladium-catalyzed strategies for quinoline synthesis, emphasizing oxidative and tandem annulation methods. Reactions are categorized by substitution patterns on the quinoline scaffold—namely 2-aryl, 4-substituted, 2,3-, 2,4- and 3,4-disubstituted, 2,3,4-trisubstituted, and annulated derivatives—to facilitate mechanistic comparisons and highlight structural scope. Together, the reviewed strategies showcase the range of mechanistic possibilities available for constructing quinoline scaffolds via palladium catalysis. Overall, these Pd-catalyzed approaches offer powerful and versatile tools for the synthesis of complex quinoline frameworks, providing valuable alternatives to classical heterocycle forming reactions. Full article
(This article belongs to the Special Issue Feature Review Papers on Catalysis in Organic and Polymer Chemistry)
Show Figures

Figure 1

15 pages, 1612 KB  
Review
End-Functionalization in Coordination Chain Transfer Polymerization of Conjugated Dienes
by Lijia Liu, Wenpeng Zhao, Feng Wang, Xuequan Zhang and Heng Liu
Catalysts 2026, 16(2), 121; https://doi.org/10.3390/catal16020121 - 27 Jan 2026
Viewed by 325
Abstract
Coordination chain transfer polymerization (CCTP) has emerged as an efficient and controllable polymerization strategy that also allows for efficient in situ end-functionalization of polydienes through the highly reactive metal–carbon bonds that are generated during the CCTP process. Despite substantial progress in CCTP chemistry, [...] Read more.
Coordination chain transfer polymerization (CCTP) has emerged as an efficient and controllable polymerization strategy that also allows for efficient in situ end-functionalization of polydienes through the highly reactive metal–carbon bonds that are generated during the CCTP process. Despite substantial progress in CCTP chemistry, reviews focusing specifically on its application to diene monomers—and particularly on its effectiveness in producing end-functionalized polydiene elastomers—remain scarce. To address this gap, this review summarizes the advances achieved over the past decade in the end-functionalization of polydienes via CCTP. We begin with a brief overview of the fundamental principles and core mechanisms of CCTP, followed by a systematic discussion of functionalization strategies for key diene monomers, including isoprene and butadiene. Finally, we highlight the existing challenges in this field and provide our perspectives on future research directions. Full article
(This article belongs to the Special Issue Feature Review Papers on Catalysis in Organic and Polymer Chemistry)
Show Figures

Graphical abstract

41 pages, 4802 KB  
Review
PdII Catalysis: Recent Advances in the Intramolecular Wacker-Type Reaction of Alkenols and Related Domino Reactions
by Jacques Muzart
Catalysts 2025, 15(9), 845; https://doi.org/10.3390/catal15090845 - 2 Sep 2025
Viewed by 1289
Abstract
This review surveys the last twenty years of the PdII-catalysed oxaheterocyclisation of alkenes bearing a hydroxylated tether as well as the plausible subsequent in situ reactions, the intramolecular C–O bond formation being the first step of a domino process involving, among [...] Read more.
This review surveys the last twenty years of the PdII-catalysed oxaheterocyclisation of alkenes bearing a hydroxylated tether as well as the plausible subsequent in situ reactions, the intramolecular C–O bond formation being the first step of a domino process involving, among others, the Heck reaction, etherification, esterification and lactonisation. Versatile intermediates usable for the total synthesis of natural products have been thus produced. The proposed reaction mechanisms are highlighted with, as far as possible, personal comments. Full article
(This article belongs to the Special Issue Feature Review Papers on Catalysis in Organic and Polymer Chemistry)
Show Figures

Graphical abstract

Back to TopTop