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Electrocatalytic Cross-Coupling Reactions with Heterogeneous Single Atom Catalysts

Lead Research Organisation: University of Leicester
Department Name: Chemistry

Abstract

Fine chemicals make up the largest portion of the global chemicals market with their revenues expected to grow to $220bn by 2024. Examples of important classes of fine chemicals, are pharmaceuticals, agrochemicals, flavours and fragrances and speciality materials (e.g., polymers). With the increasing attention on energy usage, environmental impact and safety, there is an urgent need to develop new, mild and efficient synthetic process for sustainable fine chemicals synthesis. There has been a remarkable renaissance of electrochemical catalysis, with researchers exploring how fine chemicals can be synthesised with using electrictricity as a reagent. These energy efficient, electricity-driven processes can be easily integrated with renewable energy sources and avoid the use of dangerous and toxic chemicals, which makes them a powerful green tool for chemical synthesis. However, at present, electrocatalytic methods typically utilise so called homogeneous catalytic systems, which requires transition metal catalysts, whereby all of the catalyst is fully dissolved in the reaction mixtures. These systems often suffer from high catalyst loadings due to their limited stability under the reaction conditions. Furthermore, the expensive homogeneous catalyst can only be used once due to the challenges associated with catalyst separation and recycling.

With the rapid growth of nanoscience, heterogeneous catalysts have been exploited to tackle the aforementioned problems. Although they are stable and conveniently recyclable, their overall catalytic efficiencies are usually inferior to their homogeneous counterparts. In recent years, a new class of heterogeneous catalysts, namely single-atom catalysts (SACs), which are emerging as a new frontier in catalysis science. In this case, the active metal centre of the catalyst exists as isolated single atoms, which are stabilized by the support material., SACs can serve as a bridge between homogeneous and heterogeneous catalysts with the possibility of integrating the merits of both types of catalysts such as high activity, selectivity, stability and reusability. Indeed, many breakthroughs in clean energy conversion reactions (e.g., oxygen reduction, hydrogen evolution, CO2 reduction) using SACs has been reported recently. These have demonstrated their great potential in electrochemical applications, but electrocatalytic fine chemical synthesis using SACs remains unexplored.

As the most frequently used class of reaction in pharmaceutical synthesis, the so called cross-coupling reactions were recognized in 2010 by the Nobel Prize in Chemistry. In this project, we will exploit the inherent properties of SACs to revolutionise fine chemical synthesis by creating completely new heterogeneous electrochemical cross-coupling reactions as proof-of-concept examples. Through newly forged collaborations with Prof. Yanqiang Huang from Dalian Institute of Chemical Physics (DICP, the birthplace of SACs concept), Prof. Karl Ryder (UoL) and MOF Technologies, novel nickel based SACs will be synthesized using metal organic frameworks (MOFs) as precursors, and the mechanisms of these SACs catalysed reactions will be studied using modern material characterization techniques This project is highly interdisciplinary and at the intersection of cutting-edge organic synthesis, electrochemistry, materials science and state-of-the-art heterogeneous catalysis. Success in the area will bring both economic and environmental benefits and enable the manufacture of fine chemicals, such as pharmaceuticals, to be prepared using more sustainable processes. The understanding of catalyst structure-performance relationships and reaction mechanisms will enable the design of new SACs systems, that can be exploited for a range of chemical reactions, broadening its impact.

Publications

10 25 50
 
Description During the Early Career Researcher International Collaboration Grant, we successfully established research collaborations with Prof. Jianguo Wang and Prof. Zhenlu Shen at Zhejiang University of Technology (ZUT) and Prof. Yanqiang Huang at Dalian University of Technology (DUT). The primary objective of this collaboration is to develop novel synthetic methods for fine chemical production using single-atom catalysts (SACs) under electrocatalytic conditions.

As a result of this collaboration, we have developed an electrocatalytic synthetic method for the semi-hydrogenation of alkynes to alkenes using water as a hydrogen source, catalyzed by Pd-based heterogeneous catalysts. This work has been successfully published in a peer-reviewed journal (J. Chem. Eng. 489, 2024, 151271). Building on this achievement, we are currently exploring the use of SACs for electrocatalytic organic synthesis, particularly in cross-coupling reactions. This ongoing project in my lab aims to establish a practical and scalable approach for C-C bond formation using sustainable electrocatalytic methods.

In parallel, we expanded our investigation to explore the potential of using the SACs we synthesized for photocatalytic cross-coupling reactions. Surprisingly, we discovered that single-atom nickel catalysts anchored on carbon nitride materials exhibited remarkable photocatalytic activity. This novel method allows the formation of C-C bonds between two distinct electrophiles under visible-light irradiation, using a recyclable and stable heterogeneous catalyst. This discovery not only provides a practical and sustainable method for C-C bond formation but also addresses the long-standing challenge of developing efficient and reusable photocatalysts. We anticipate publishing this work in a high-impact journal in the near future.

Additionally, we unexpectedly found that the SACs we prepared demonstrated excellent catalytic activity for the aerobic oxidation of amines to nitriles and imines, which are key functional groups in organic synthesis and bioactive compound production. This finding has opened new research directions, and we are now working towards optimizing this method to achieve highly efficient and selective N-based compound synthesis using air as a green oxidant. This work has the potential to lead to impactful publications and practical industrial applications in the near future.

Collectively, the outcomes from these collaborations have greatly advanced our understanding of SACs in both electrocatalytic and photocatalytic organic synthesis. Moving forward, we plan to deepen our collaboration with Prof. Jianguo Wang, Prof. Zhenlu Shen, and Prof. Yanqiang Huang to conduct in-depth mechanistic studies and further optimize the catalytic performance of SACs, aiming to translate these findings into practical and scalable methodologies for sustainable fine chemical synthesis.
Exploitation Route The outcomes of this funding have the potential to be taken forward and put to use by others in several impactful ways:

1. Advancement of Green Chemistry: The development of single-atom catalysts (SACs) for organic synthesis under electrocatalytic and photocatalytic conditions provides a sustainable and energy-efficient alternative to traditional methods, particularly in fine chemical synthesis. The use of visible light and air as green oxidants, coupled with recyclable catalysts, aligns with the growing demand for eco-friendly, low-energy chemical processes. Other researchers and industries can adopt these methodologies to reduce the carbon footprint in the production of pharmaceuticals, agricultural chemicals, and other fine chemicals.
2. Catalyst Development: The insights gained from the preparation and characterization of SACs can contribute to the development of more efficient, selective, and stable catalysts for a variety of organic reactions. This can be applied in the fields of catalysis, materials science, and industrial chemistry. Researchers can build on this work to design SACs for other reactions beyond those explored in this project, expanding the application of SACs in diverse chemical transformations.
3. Innovation in Cross-Coupling Reactions: The discovery of single-atom Ni catalysts for photocatalytic cross-coupling reactions can be widely adopted by researchers working in organic synthesis. This strategy allows for the formation of C-C bonds with the advantage of using visible light as an energy source, making it an attractive tool for sustainable organic synthesis. Other groups can utilize this methodology for developing new routes to complex molecules, enabling more efficient and environmentally friendly synthesis of various bioactive compounds.
4. Collaborative Mechanistic Studies: The collaborations with Prof. Jianguo Wang, Prof. Zhenlu Shen, and Prof. Yanqiang Huang provide a foundation for further research in understanding the mechanisms of electrocatalytic and photocatalytic reactions. Other researchers can leverage these collaborations and mechanistic insights to explore new reaction pathways and improve reaction efficiencies. The detailed studies of SACs and their catalytic behavior under various conditions will help advance the broader understanding of catalyst design and reaction optimization.
5. Training the Next Generation of Researchers: Through the training of postdoctoral researchers and PhD students in these advanced catalytic techniques, the research helps to build expertise in a rapidly growing area of chemistry. These trained researchers will bring valuable skills to academia, industry, and research institutions, contributing to the continued development of sustainable chemical methods.
6. Impact on Industry: The scalable and efficient methods for producing fine chemicals, especially with sustainable catalysts and under mild conditions, can directly benefit industries such as pharmaceuticals, agrochemicals, and specialty chemicals. The potential to reduce costs, improve efficiency, and reduce environmental impact makes these methods attractive to industrial applications. Companies looking to develop more sustainable production processes can incorporate these findings into their R&D strategies.
7. Promoting Future Collaborations: The multi-disciplinary nature of this research, combining catalysis, materials science, and green chemistry, sets the stage for future collaborations between researchers in these fields. The ongoing work with the collaborators, along with the development of new catalytic systems, may lead to further breakthroughs that can be shared across research groups and industries, encouraging a collaborative approach to solving global challenges in chemical synthesis.
Sectors Chemicals

Environment

Healthcare

Manufacturing

including Industrial Biotechology

Pharmaceuticals and Medical Biotechnology

 
Description Influence on training of researchers
Geographic Reach Multiple continents/international 
Policy Influence Type Influenced training of practitioners or researchers
Impact The application of single-atom catalysts (SACs) for the synthesis of fine chemicals under both electrocatalytic and photocatalytic conditions remains highly uncommon in both academia and industry. The training provided to Dr. Sonia Sharma, as well as the PhD students involved in this program, has equipped them with specialized expertise in this emerging area. This includes the development of next-generation synthetic methods utilizing electricity as a clean energy input and SACs as efficient, recyclable heterogeneous catalysts for organic synthesis. The outcomes of this training and research are expected to generate a significant economic impact by promoting more sustainable and cost-effective synthetic routes for fine chemicals production, including pharmaceuticals and agrochemicals. By reducing reliance on fossil fuel-derived energy and minimizing catalyst consumption, this approach will also contribute to reducing the carbon footprint associated with fine chemical synthesis. Furthermore, the development of skilled researchers with expertise in electrocatalysis and SACs will strengthen the UK's research capacity in sustainable synthesis, fostering future industrial applications and collaborations aimed at decarbonizing the chemical manufacturing sector.
 
Description Collaboration with Dalian Institute of Chemical Physics 
Organisation Dalian Institute of Chemical Physics
Country China 
Sector Private 
PI Contribution Since being awarded the Early Career Researcher International Collaboration Grant, we have initiated a research collaboration with Prof. Yanqiang Huang from the Dalian Institute of Chemical Physics (DICP). Prof. Huang's group specializes in the development of single-atom catalysts (SACs) for electrocatalytic activation of small molecules, such as CO2 reduction. During our collaboration, we proposed the potential application of SACs in organic synthesis, particularly for cross-coupling reactions under electrocatalytic conditions, aiming to expand the utilization of SACs beyond small molecule activation. As part of this collaboration, we successfully replicated some of the SACs previously reported by Prof. Huang's group and applied them in electrocatalytic cross-coupling reactions. Notably, given the mechanistic similarity between photocatalytic and electrocatalytic processes, both of which involve the generation of organic radicals, we also explored the use of nickel-based carbon nitride catalysts for cross-coupling reactions under photocatalytic conditions. This exploration led to the development of the first cross-electrophile coupling reaction under photocatalytic conditions using single-atom Ni-based catalysts. This collaborative work has significantly expanded the scope of SACs from small molecule activation to sustainable organic synthesis and has opened new avenues for cross-coupling reactions under photocatalytic and electrocatalytic conditions.
Collaborator Contribution Prof. Yanqiang Huang has also provided valuable guidance on the synthesis of nickel-based single-atom catalysts (SACs) supported on N-doped carbon materials and carbon nitrides, which significantly contributed to the development of our catalytic system. Given Prof. Huang's extensive expertise in SAC characterization, his group has also offered support in performing in situ X-ray absorption fine structure (XAFS) spectroscopy to gain mechanistic insights into both electrocatalytic and photocatalytic reactions. Moving forward, we plan to strengthen our collaboration with Prof. Huang's group by conducting comprehensive mechanistic studies using in situ XAFS and other advanced characterization techniques. These studies will enable us to gain a deeper understanding of the reaction pathways and catalytic behavior of single-atom nickel catalysts under both photocatalytic and electrocatalytic conditions. We anticipate that this collaborative effort will lead to high-impact publications in reputable journals, further advancing the application of SACs in sustainable organic synthesis.
Impact This collaboration represents a multi-disciplinary research effort that bridges materials science, electrocatalysis, and organic synthesis. Prof. Yanqiang Huang, an expert in materials science and small molecule activation under electrocatalytic conditions, provides critical guidance in the design, synthesis, and characterization of single-atom catalysts (SACs). His expertise in in situ X-ray absorption fine structure (XAFS) spectroscopy further supports the mechanistic understanding of catalytic processes. On the other hand, my group, has extensive experience in organic synthesis, particularly in oxidation reactions and cross-coupling methodologies. The combination of these complementary expertise has enabled us to explore the potential application of SACs in cross-coupling reactions under electrocatalytic conditions. This joint effort not only expands the application of SACs beyond small molecule activation but also provides a promising approach for developing sustainable and efficient catalytic systems for C-C and C-heteroatom bond formation. We anticipate that continued collaboration will lead to a deeper understanding of the catalytic mechanisms and the development of high-impact publications in this emerging research area.
Start Year 2024
 
Description Collaboration with Zhejiang University of Technology 
Organisation Zhejiang University of Technology
Country China 
Sector Academic/University 
PI Contribution Since I was awarded the Early Career Researcher International Collaboration Grant, I have established a research collaboration with Prof. Jianguo Wang at Zhejiang University of Technology (ZUT). This collaboration has led to the publication of a research paper on the semihydrogenation of alkynes to alkenes via an electrocatalytic approach using nano-Pd heterogeneous catalysts (J. Chem. Eng. 489 2024, 151271). As part of this collaboration, one of Prof. Wang's PhD students, Guoliang Wang, was funded by ZUT to visit the University of Leicester for six months. During his visit, the student conducted electrocatalytic experiments for this project, while my group provided support in the isolation and characterisation of organic compounds, as well as in designing control experiments to elucidate the reaction mechanism. This collaboration has strengthened the exchange of knowledge and technical expertise between our groups and contributed to the successful advancement of this research. In addition, I have contributed my expertise in kinetic interpretation of organic synthesis to one of Prof. Jianguo Wang's projects on photocatalytic H2O2 synthesis using carbon nitride materials. My involvement focused on analyzing reaction kinetics and providing insights into the factors influencing catalytic performance. This collaboration has resulted in a joint publication in AIChE Journal (AIChE J. 71, 2025, e18692), further strengthening our research partnership.
Collaborator Contribution The visiting student, Guoliang Wang, also contributed to my group by assisting in the design of electrocatalytic experiments and transferring knowledge on performing organic synthesis (e.g., cross-coupling) under electrocatalytic conditions, which has greatly benefited my group's research capabilities in this area. In addition, Prof. Jianguo Wang, an expert in density functional theory (DFT), has expressed strong interest in collaborating on the mechanistic study of our ongoing project at the University of Leicester (UoL). Recently, one of my PhD students, Yuhe Gao, developed a novel approach for the oxidation of amines to nitriles and imines using a single-atom iron catalyst. During the study, we observed that the addition of water significantly enhanced both the yield of the desired products and the catalytic activity. To gain deeper insights into the promotional role of water, Prof. Wang has agreed to support us by performing DFT calculations to elucidate the underlying reaction mechanism. We anticipate that this collaborative effort will significantly enhance our understanding of the reaction pathway and facilitate further optimization of our catalytic system.
Impact In terms of publication: (1) Synergistic photocatalytic synthesis of H2O2: Mechanistic insights and sustainable applications, AIChE J. 2025, 71, e18692 (2) Efficient electrocatalytic alkyne Semi-Hydrogenation and deuteration using Pd/PANI catalysts supported on nickel foam, Chem. Eng. J. 489, 2024, 151271
Start Year 2024