| Dipl.-Chem. Univ. (Chemie) | Universität Regensburg (1982-1987) |
| Dr. rer. nat. | Institut für Anorganische Chemie, Universität Regensburg (1987-1989) |
| Postdoc | Dyson Perrins Laboratory for Organic Chemistry, University of Oxford, UK (1990) |
| Stipendium | Liebig-Stipendiat des Fonds der Chemischen Industrie, Universität Regensburg (1991-1992) |
| Wiss. MA | Max-Planck-Arbeitsgruppe CO2-Chemie, Friedrich-Schiller-Universität Jena (1992-1995) |
| Habilitation | Friedrich-Schiller-Universität Jena (1995) |
| Privatdozent | Friedrich-Schiller-Universität Jena (1995) |
| Gruppenleiter | Abteilung 'Organische Synthese', Max-Planck-Institut für Kohlenforschung, Mülheim/Ruhr (1995-1998) |
| Leiter des Technikums | Max-Planck-Institut für Kohlenforschung, Mülheim/Ruhr (1998-2002) |
| Lehrstuhlvertretung | Technische Chemie und Petrolchemie, RWTH Aachen (2000-2002) |
| Lehrstuhlinhaber | Technische Chemie und Petrolchemie, Institut für Technische und Makromolekulare Chemie, RWTH Aachen (seit 2002) |
| Ext. Wiss. Mitglied | Max-Planck-Institut für Kohlenforschung, Mülheim/Ruhr (2002-2017) |
| Direktor | Molekulare Katalyse, MPI CEC (seit 2017) |
Full publications list | ORCID | ResearcherID
2026
Hu, J.; Lacroix, L. M.; Johny, J.; Ghosh, S.; Wolf, E. H.; Ji, J.; Lin, S.-H.; Durai, M.; Schöne, A. B.; Hetaba, W.; Ruland, H.; Leitner, W.; Bordet, A. (2026). Low-Temperature Reverse Water-Gas Shift Enabled by Magnetically Induced Catalysis, Angewandte Chemie-International Edition, Early Access. doi:10.1002/anie.202523576.
2025
2024
2023
2018-2022
Prof. Leitner ist seit 2002 Lehrstuhlinhaber und Professor für Technische Chemie und Petrolchemie an der RWTH Aachen.
Webseite: RWTH Aachen - Lehrstuhl für Technische Chemie und Petrolchemie
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Gruppenleiter*innen
Dr. Alexis BordetPhD Studierende
Sihana AhmediResearch in the Department of Molecular Catalysis ranges from the design and preparation of catalytically active metal complexes and materials, over the optimization of existing and exploration of novel synthetic pathways, to the development of advanced reaction-engineering concepts. Rooted in the field of organometallic chemistry, we embrace the concept of Green Chemistry as guiding principle for our catalysis research. We view the increasing de-carbonization of the electricity sector as opportunity for the de-fossilization of the sectors mobility and chemistry.[i] Valorising carbon dioxide and biomass through catalytic reduction processes using either H2 or e-/H+ offers not only non-fossil entries into existing chemical value chains, but holds the exciting opportunity to strive for shorter synthetic pathways, more effective processes, and better products (Figure 1).2,3
In order to turn the challenges of the transition from fossil to renewable into strategic opportunities for innovation, we identified three main objectives for the research in our team (Figure 2).
From Cracking to Building
Whereas the key entry point into the petrochemical value chain are processes designed to crack C-C and C-H bonds in long-chain energy rich molecules, synthetic pathways based on renewable energy and feedstocks build molecular complexity from C1 building blocks derived from CO2 and/or by re-organising functionalities in bio-based substrates. Recent examples include the synthesis of carboxylic acids by catalytic carbonylation of alcohols using CO2/H2 as CO source.4,5 The step-wise C1 elongation of alcohols via a repetitive dehydration-hydroformylation-reduction sequence was achieved through combination of molecular and reaction engineering competence.6 Fundamental aspects of catalyst activation and deactivation upon direct use of CO produced by low-temperature CO2 electrolysis in Pd-catalysed carbonylation reactions are part of the Kopernikus project “Power-to-ValueChemicals”.7
As long-term goal, an integrated pathway and product design process for individual chemical products and even multi-component mixtures as in fuels comes into reach. Based on fundamental studies from our team on integrating Fischer-Tropsch synthesis with hydroformylation,8 this was demonstrated for so-called “HyFiT fuels” by a highly interdisciplinary collaboration in the Fuel and Chemical Science Center (FSC2) comprising catalytic production, combustion science, and life cycle assessment (Figure 3).9 Olefins formed as primary products during chain growth over the heterogeneous Fischer-Tropsch catalysts are in situ converted to C1 elongated alcohols by a homogeneous catalyst in solution. Both coupled reactions require syngas in a CO/H2 ratio of 1:2 as feedstock. The concept is pursued further with international partners in the EU project “E-Tandem” in the team led by PD Dr. Andreas Vorholt.
There is a rapidly growing mechanistic understanding of catalytic transformations aiming at the use of renewable building blocks from experiment and theory. Rooted in organometallic chemistry, we are aiming to translate such knowledge between different approaches in catalysis to develop improved catalytic systems for established reactions and ultimately arrive at rational design or even prediction of novel transformations. The previously introduced dissection10 of electrochemical CO2 reduction pathways either through formation of metal hydride complexes (ETH) or by direct electron transfer from metal to carbon (ETM) could be unravelled in detail for low-valent rhodium complexes.11 Ruthenium nanoparticles were deposited on molecularly modified supports comprising functionalities known to stabilize formic acid in solution phase catalysis, thus pushing the limits for heterogeneous catalysts in CO2 hydrogenation to formate in terms of activity12 and stability.13
The interconversion of C1 products along the various reduction levels between CO2 and CH4 is particularly relevant for chemical energy conversion.14 Manganese pincer complexes have proven particularly powerful in this context. We exploit systematically the diagonal relationship between Mn+ and Ru2+ in the periodic table, resulting in similarities for H-H bond activation coupled with a significantly more moderate CO binding affinity. Our recent studies show that Mn-MACHO type complexes exhibit not only substantial catalytic activity for the catalytic synthesis of MeOH from syngas,15 but also show high stability under continuous operation with turnover numbers limited solely by cannibalistic side reactions of the base co-catalyst rather than the organometallic active species.16 Notably, the understanding of the basic catalytic cycles has already led to the rational design of new synthetic pathways including the recently developed “methanolation” of olefins as low-temperature and low-pressure alternative to reductive hydroformylation (Figure 4).17
A long-term vision is to translate the analytical knowledge on molecular mechanisms into predictive approaches using computational chemistry for the identification of catalysts or lead structures for currently unknown reactions. To this end, we have devised a catalytic cycle for the carboxylation of C-H bonds with CO2 composed of elementary steps analogous to the well-established catalytic hydrogenation of CO2 to formic acid (Figure 5). The computational screening focused on the turnover determining intermediates and transition states to minimize the energy span of the cycle for pre-selected structural motifs. In a proof-of-concept study, the collaboration of Dr. Markus Hölscher (RWTH Aachen University) and Dr. Gregor Kemper resulted in the first carboxylation of non-activated aromatic C-H bonds, and its synthetic potential could be demonstrated using organometallic Pd-catalysts.18
Individual processes of the petrochemical value chain are typically based on catalysts that have been optimized for a specific task very precisely to operate largely under static conditions that maximise the output of a single product. With the coupling to renewable and hence fluctuating energy sources and an increasing diversity and variation of feedstock qualities, catalytic systems that can be adjusted or even self-adjust to dynamic changes in real time may become attractive alternatives.19 This includes the possibility of flexible customized production of different products from a single starting material reacting for example on variations in energy availability or costs.
Our approach in this area capitalizes on the organometallic approach to generate catalytic materials comprising defined metal nanoparticles on functional supports.20 Meanwhile, a large portfolio of mono- and bimetallic as well as metal-phosphide nanoparticles has been generated and integrated with molecularly modified oxidic and carbon-based supports to generate catalysts exhibiting challenging selectivities and allowing novel tandem reaction sequences. A most recent example is the controlled synthesis of ruthenium-phosphide RuxP100-x based catalysts for the selective hydrogenation of heteroarenes (Figure 6).21
While those systems are optimized for maximum performance in specific reaction types, adaptive systems are designed to be reversibly adjustable between different states of performance. The reversible formation of surface formate species over metal nanoparticles in the presence of H2 and CO2 provides a simple and versatile method to adaptively control selectivity in the hydrogenation of multifunctional substrates. Simple introducing CO2 in the H2 feed gas reversibly shuts down C=O22 or arene23 hydrogenation without significantly affecting the rate of hydrogenation of other functional groups (Figure 7). Experimental and computational mechanistic studies support selective blocking by surface formate species as the main contribution to the selectivity switch.24 Since the first demonstration of the concept using rather complex support materials, the catalysts have now been significantly simplified with the prospect to use even commercial catalysts in the future.
Magnetically induced catalysis has proven extremely powerful in the context of adaptive catalysis and is now developed strategically with support from the Gordon and Betty Moore Foundation in the team lead by Dr. Alexis Bordet. The prospective of localised and highly dynamic heating of the catalyst material in cold reaction environments has been demonstrated for iron carbide nanoparticles as heating agents, where catalytic activity originates either intrinsically from ICNPs, from their decoration with active metals, or from their deposition on commercial metal catalyst, as summarized in a recent perspective article.25 Opening an additional dimension, it could be demonstrated that the technique allows to decouple the reaction equilibrium at the hot catalyst surface and the phase equilibrium in the cold environment to enable low-temperature reverse water-gas-shift reaction (Figure 8).26
The three main research objectives are addressed in a matrix-type organisation in competence-oriented sub-groups led by senior scientists as further elaborated on their respective websites. The team Multiphase Catalysis is headed by Andreas J. Vorholt, and Multifunctional Catalytic Systems by Alexis Bordet. Since the appointment of Nicholas Kaeffer as CNRS junior professor in 2025, the sub-group on Organometallic CO2 Chemistry and Electrochemistry is led jointly by Gregor Kemper and Anne-Christine Kick. The team collaborates closely with Markus Hölscher at RWTH Aachen University in the area of Computational Chemistry. All PhD and postdoc projects are embedded in one of the groups ensuring close day-to-day supervision. The departmental Analytical Services led by Justus Werkmeister ensures cutting-edge infrastructure and high-level competences for offline analysis and online monitoring. The entire team meets once per week in the Department Seminar, and individual progress is discussed in regular meetings between the director, group leader and student or postdoc. The resulting natural synergies between the groups is reflected in numerous joint projects and publications within the team, the institute, and the entire MPI CEC scientific ecosystem.
In addition to the documentation in scientific publications and conference contributions, the fundamental insights and methodological progress developed in the research efforts also form the basis of intellectual property secured in patent applications where appropriate. Complementing conventional ways of translation through industrial collaborations, they find increasingly interest by next-generation researchers as basis for start-up initiatives. The spin-off from the Kopernikus Project “Power-to-Polymers” works on CO2-based polymers for adhesive and lubricant applications, and has recently been able to produce a batch of their materials using “green” methanol from the Carbon2Chem project as starting material. The start-up team “C4Value” originating from the Multiphase Catalysis group develops a new catalyst platform for the production of butandiols and butadiene from biogenic ethanol.
In conclusion, the research in the Department of Molecular Catalysis is characterised by complementary individual competences, close collaboration, shared expertise, and sustained commitment from all contributors. Or in the words of Nelson Mandela: It always seems impossible – until its done.
[1] Anastas, P. T., Leitner, W. (2025). Transform the World through Chemistry. Angewandte Chemie International Edition in English, 64 (33), e202512699. doi:10.1002/anie.202512699.
[2] Leitner, W. (2024). Carbon dioxide and hydrogen as building blocks for a sustainable interface of energy and chemistry. Philosophical Transactions of the Royal Society A - Mathematical Physical and Engineering Sciences, 382 (2282). doi:10.1098/rsta.2023.0266.
[3] Leclerc, H. O., Erythropel, H. C., Backhaus, A., Lee, D. S., Judd, D. R., Paulsen, M. M., Ishii, M., Long, A., Ratjen, L., Bertho, G. G., Deetman, C., Du, Y., Lane, M. K. M., Petrovic, P. V., Champlin, A. T., Bordet, A., Kaeffer, N., Kemper, G., Zimmerman, J. B., Leitner, W., Anastas, P. T. (2024). The CO2 Tree: The Potential for Carbon Dioxide Utilization Pathways. ACS Sustainable Chemistry & Engineering, 13 (1), 5-29. doi:10.1021/acssuschemeng.4c07582.
[4] Jurling-Will, P., Linnartz, N. J., Francio, G., Leitner, W. (2025). Catalytic Synthesis of Acetic Acid from Methanol Using Formic Acid as a Renewable CO Source. Energy & Fuels, 39 (47), 22645-22651. doi:10.1021/acs.energyfuels.5c04169.
[5] Solmi, M. V., Vossen, J. T., Schmitz, M., Vorholt, A. J., Leitner, W. (2024). Catalytic synthesis of carboxylic acids from oxygenated substrates using CO2 and H2 as C1 building blocks. Green Chemistry, 26 (12), 7302-7311. doi:10.1039/d4gc01732c.
[6] Vossen, J. T., Leitner, W., Vorholt, A. J. (2025). Selective Construction of Linear Carbon Chains Using Synthesis Gas (CO/H2) for C1-Elongation via a Three-Step Reaction Cycle. ACS Sustainable Chemistry & Engineering, 13 (9), 3797-3805. doi:10.1021/acssuschemeng.4c10677.
[7] Wessel, N., Medhekar, R. S., Sonnenberg, M., Stieber, H., Leitner, W., Vorholt, A. J. (2024). Catalyst in Sight: The Use of Benchtop NMR Spectrometers to Maintain the Activity of Pd-PPh3 Catalysts. ACS Catalysis, 14 (14), 10679-10688. doi:10.1021/acscatal.4c02606.
[8] Jeske, K., Rösler, T., Belleflamme, M., Rodenas, T., Fischer, N., Claeys, M., Leitner, W., Vorholt, A. J., Prieto, G. (2022). Direct Conversion of Syngas to Higher Alcohols via Tandem Integration of Fischer-Tropsch Synthesis and Reductive Hydroformylation. Angewandte Chemie, International Edition in English, 61, e202201004. doi:10.1002/anie.202201004.
[9] Voelker, S., Groll, N., Bachmann, M., Mueller, L., Neumann, M., Kossioris, T., Muthyala, P., Lehrheuer, B., Hofmeister, M., Vorholt, A., Schmitz, K., Pischinger, S., Leitner, W., Bardow, A. (2024). Towards carbon-neutral and clean propulsion in heavy-duty transportation with hydroformylated Fischer-Tropsch fuels. Nature Energy, 9 (10), 1220-1229. doi:10.1038/s41560-024-01581-z.
[10] Kinzel, N. W., Werlé, C., Leitner, W. (2021). Transition Metal Complexes as Catalysts for the Electroconversion of CO2: An Organometallic Perspective. Angewandte Chemie, International Edition in English, 60, 11268-11686. https://doi.org/10.1002/anie.202006988
[11] Kick, A. C., Schatz, M., Kahl, C., Hölscher, M., Eichel, R. A., Granwehr, J., Kaeffer, N., Leitner, W. (2026). Mapping proton and carbon dioxide electrocatalytic reductions at a Rh complex by in situ spectroelectrochemical NMR. Chemical Science, Advanced Article. doi:10.1039/d5sc05744b.
[12] Anandaraj, S. J. L., Kang, L., DeBeer, S., Bordet, A., Leitner, W. (2023). Catalytic Hydrogenation of CO2 to Formate Using Ruthenium Nanoparticles Immobilized on Supported Ionic Liquid Phases. Small, 19, 2206806, pp. 1-10. doi:10.1002/smll.202206806.
[13] Antil, N. L., Anandaraj, S. J., Kang, L., Ghazi Zahedi, H., DeBeer, S., Leitner, W., Bordet, A. (2025). Ruthenium Nanoparticles on Water-Stable Supported Ionic Liquid Phases as Catalytic Systems for Aqueous Phase CO2 Hydrogenation. ACS Catalysis, 15 (17), 14601-14610. doi:10.1021/acscatal.5c03605.
[14] Cramer, H. H., Das, S., Wodrich, M. D., Corminboeuf, C., Werlé, C., Leitner, W. (2023). Theory-guided development of homogeneous catalysts for the reduction of CO2 to formate, formaldehyde, and methanol derivatives. Chemical Science, 14 (11), 2799-2807. doi:10.1039/d2sc06793e.
[15] Stahl, S., Wessel, N., Vorholt, A. J., Leitner, W. (2024). Liquid-phase hydrogenation of carbon monoxide to methanol using a recyclable manganese-based catalytic system. Green Chemistry, 26, 7799-7805. doi:10.1039/d4gc01050g.
[16] Stahl, S., Steinwachs, L., Leitner, W., Vorholt, A. J. (2026). Continuously operated liquid-phase methanol synthesis uncovering the de-/activation pathways of a molecular manganese catalyst system. Green Chemistry, advance article. doi:10.1039/d5gc05072c.
[17] Stahl, S., Vossen, J. T., Popp, S., Leitner, W., Vorholt, A. J. (2025). Methanolation of Olefins: Low-Pressure Synthesis of Alcohols by the Formal Addition of Methanol to Olefins. Angewandte Chemie International Edition in English, 64 (7), e202418984. doi:10.1002/anie.202418984.
[18] Kemper, G., Hölscher, M., Leitner, W. (2023). Pd(II)-catalyzed carboxylation of aromatic C-H bonds with CO2. Science Advances,9 (5): eadf2966, pp. 1-10. doi:10.1126/sciadv.adf2966.
[19] Bordet, A., Leitner, W. (2023). Adaptive Catalytic Systems for Chemical Energy Conversion.Angewandte Chemie, International Edition in English, 62, e202301956. doi:10.1002/anie.202301956.
[20] Bordet, A., Leitner, W. (2021). Metal Nanoparticles Immobilized on Molecularly Modified Surfaces: Versatile Catalytic Systems for Controlled Hydrogenation and Hydrogenolysis. Accounts of Chemical Research, 54,2144-2157. doi:10.1021/acs.accounts.1c00013.
[21] Zahedi, H. G., Hertel, J, Paul, B., Kang, L., Johny, J., Wu, Y., Wiegand, T., DeBeer, S., Leitner, W., Bordet, A. (2026). Selective Hydrogenation of Heteroarenes Using Supported Ruthenium Phosphide Nanoparticle Catalysts. Journal of the American Chemical Society, 148 (1), 766–777. https://doi.org/10.1021/jacs.5c16144
[22] Bordet, A., El Sayed, S., Sanger, M., Boniface, K. J., Kalsi, D., Luska, K. L., Jessop, P.; Leitner,W. (2021) Selectivity control in hydrogenation through adaptive catalysis using ruthenium nanoparticles on a CO2-responsive support. Nature Chemistry,13, 916-922. doi:10.1038/s41557-021-00735-w.
[23] Zhang, Y., El Sayed, S., Kang, L., Sanger, M., Wiegand, T., Jessop, P. G., DeBeer, S., Bordet, A., Leitner, W. (2023). Adaptive Catalysts for the Selective Hydrogenation of Bicyclic Heteroaromatics using Ruthenium Nanoparticles on a CO2-Responsive Support. Angewandte Chemie, International Edition in English,,62, e202311427. doi:10.1002/anie.202311427.
[24] Zhang, Y. Y., Levin, N., Kang, L. Q., Müller, F., Zobel, M., DeBeer, S., Leitner, W., Bordet, A. (2024). Design and Understanding of Adaptive Hydrogenation Catalysts Triggered by the H2/CO2-Formic Acid Equilibrium. Journal of the American Chemical Society, 146 (44), 30057-30067. doi:10.1021/jacs.4c06765.
[25] Bordet, A., Leitner, W., Chaudret, B. (2025). Magnetically Induced Catalysis: Definition, Advances, and Potential. Angewandte Chemie, International Edition in English, 64 (24), e202424151 doi:10.1002/anie.202424151.
[26] Hu, J., Lacroix, L. M., Johny, J., Ghosh, S. Wolf, E. H., Ji, J. Lin, S.-H., Durai, M. Schöne, A. B., Hetaba, W. Ruland, H., Leitner, W., Bordet, A. (2026). Low-Temperature Reverse Water–Gas Shift Enabled by Magnetically Induced Catalysis. Angewandte Chemie, International Edition in English, advance article, e23576. https://doi.org/10.1002/anie.202523576