Wortmarke der Ruhr-Universität Bochum

Lehrstuhl für Theoretische Chemie



Welcome to the Group of Dr. Michael Römelt

 


Dr. Michael Römelt 
Lehrstuhl für Theoretische Chemie 
Ruhr-Universität Bochum 
D-44780 Bochum 
Germany 
Phone: +49 (0)234 32 26749 
E-mail: michael.roemelt@theochem.ruhr-uni-bochum.de


Complex molecular systems, such as mono- and polynuclear transition metal compounds, play a key role in many areas of chemistry. They serve a multitude of purposes in various applications in homogeneous inorganic and bioinorganic catalysis as well as functional materials. Yet understanding and predicting their properties as well as their reactivity is a great challenge and one of the current frontiers of theoretical chemistry. Our research group focuses on both, the development of novel quantum chemical methods that are especially designed to tackle complex molecules and on the application of existing methods to tackle interesting chemical problems. The former aspect of our work is centered around modern multireference methods such as the density matrix renormalization group. With the help of these methods it is possible to correctly describe complex molecules that are difficult if not impossible to access using conventional methods like the complete active space self-consistent field (CASSCF). In addition to our efforts in theory development we conduct computational studies of different inorganic and organic systems using a variety of quantum chemical methods, ranging from density functional theory to high-level ab initio multireference methods. These studies concern chemical reactivities as well as spectroscopic properties. A short description of some of our recent research projects can be found below.

We have open PhD positions! If you are interested in joining our team, please contact us via michael.roemelt@theochem.ruhr-uni-bochum.de 


Research Topics

Method Development

In recent years, considerable progress was made in the field of multireference methods. In particular, the emergence of methods like the DMRG, Full-CI Quantum Monte-Carlo and various selective CI methods has opened up new perspectives and possibilities. In this regard, our group was involved in the development of approaches to incorporate dynamic electron correlation as well as spi n-orbit coupling to molecular DMRG calculations. Nevertheless, molecules with many strongly correlated electrons still pose a formidable challenge to electronic structure methods, partially owing to methodological gaps. Therefore, we have developed our own MOLBLOCK code that is dedicated to this particular kind of problem setting. Pilot studies show that it can be used to perform large-scale multireference studies on chemically relevant systems with high accuracy. Furthermore, it features the unique ASS1ST scheme that allows for a chemically motivated and physically sound selection of active orbitals. The MOLBLOCK Code will be made available here in due course.

  • A. Khedkar, M. Roemelt J. Chem. Theory Comput. 201915, 3522-3536
  • M. Roemelt, S. Guo, G. K.-L. Chan J. Chem. Phys. 2016, 144, 204113
  • M. Roemelt J. Chem. Phys. 2015143, 044112
  • M. Roemelt, V. Krewald, D. A. Pantazis  J. Chem. Theory. Comp. 201814, 166-179
 

Magnetic Properties of Transition Metal Compounds

r1

The accurate description and prediction of magnetic properties of transition metal containing complexes remains in many cases a formidable challenge for quantum chemistry. In particular, the spin-state energetics of oligonuclear exchange-coupled transition-metal complexes are difficult to calculate quantitively and sometimes even qualitatively right. Our group is involved in multiple studies of magnetic properties using modern multireference methods. For example, in a recent pilot study of a biomimetic mixed-valence Mn dimer we were able the first to calculate the exchange coupling constant of a realistically sized molecule with more than two unpaired electrons by means of wavefunction based ab initio electronic structure methods.

  • M. Roemelt, V. Krewald, D. Pantazis J. Chem. Theory Comput. 2018, 14, 166-179
  • M. Roemelt, D. A. Pantazis Adv. Theory. Simul. 20192, 1800201
  • A. Sharma, M. Roemelt, M. Reithofer, R. R. Schrock, B. M. Hoffman, F. Neese Inorg. Chem. 201756, 6906-6919

 

Selective Reduction of CO2

The selective reduction of CO2 to chemically valuable products like CO and formic acid is of high scientific, economic and social importance. In recent years we have engaged in multiple studies of molecular catalysts that are able to selectively transform CO2 into one of the aforementioned products. During those studies, our theoretical calculations were accompanied by investigations with various chemical, electrochemical and spectroscopic techniques. Eventually, the combined theoretical and experimental efforts resulted in coherent pictures about the remarkable chemical properties of the investigated systems.

  • L. Iffland, A. Khedkar, A. Petuker, M. Lieb, F. Wittkamp, M. van-Gastel, M. Roemelt, U.-P. Apfel Organometallics 201938, 289-299
  • E. Oberem, A. Rösel, A. Rosas-Hernández, T. Kull, S. Fischer, A. Spannenberg, H. Junge, M. Beller, R. Ludwig, M. Roemelt, and R. Francke Organometallics 201938, 1236-1247
  • R. Francke, B. Schille, M. Roemelt Chem. Rev. 2018118, 4631-4701
  • A. Rosas-Hernández, H. Junge, M. Beller, M. Roemelt, R. Francke Cat. Sci. Technol. 20177, 459-467

  


Print Friendly, PDF & Email