Dr. Felix Krämer

Bild von Felix Krämer

Universität Bremen

Fachbereich 2: Biologie / Chemie
Institut für Anorganische Chemie und Physikalische Chemie

Postdoc

Leobener Straße — Gebäude NW2 - Raum C2160
28359 Bremen

Tel.: +49 (0)421 218-63168

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Doktorarbeit (Karlsruhe Institute of Technology, Institute of Inorganic Chemistry):

Ambiphile Moleküle der Gruppen 13 und 14.

Masterarbeit (Karlsruhe Institute of Technology):

Inter- und Intramolekulare Frustrierte Lewis-Paare basierend auf schweren Ylenen der Gruppe 14.

Bachelorarbeit (University of Stuttgart):

Inverse Nitrid-Perowskite der Tetrele.

Publikationen

23F. Krämer, A. R. Kennedy, I. Fernández, R. E. Mulvey
A Palladium Inverse Crown: Synthesis and Characterisation.
Chem. Comm2026, 62, 1215-1219.
www
22Felix Krämer* and Robert E. Mulvey
Boosting the Nucleophilicity of the Diphenylphosphide Anion with Crown Ether Supported Heavy Alkali Metals to Facilitate Highly Efficient Catalytic Alkene Isomerisation.
Angew. Chem. Int. Ed.2026, , in Revision.
www
21F. Krämer, M. H. Crabbe, I. Fernández, R. E. Mulvey
Heavyweight Champion: Caesium Diorganophosphides Outperform Lighter Congeners in the Catalytic Hydrophosphination of Alkenes and Alkynes.
Angew. Chem. Int. ed.2025, 64, e202516376.
www
20F. Krämer, M. H. Crabbe, A. R. Kennedy, C. E. Weetman, I. Fernández, R. E. Mulvey
Crown Ether Supported Alkali Metal Phosphides: Synthesis, Structures and Bonding.
Chem. Eur. J.2025, 31, e02127 .
www
19F. Krämer, P. Weisenburger, I. Fernández, F. Breher
Stabilities and Limitations in the Reactivity of Phosphorus Ylide-Based Aluminum- and Gallium-Carbon Ambiphiles - A Combined Experimental and Computational Approach.
Eur. J. Inorg. Chem.2025, 28, e202500165.
www
18F. Krämer
Aluminum in Frustrated Lewis Pair Chemistry.
Angew. Chem. Int. ed.2024, 63, e202405207.
www
17P. Erdmann, M. Schmitt, L. M. Sigmund, F. Krämer, F. Breher, L. Greb
How to Deal with Charge in the Ranking of Lewis Acidity: Critical Evaluation of an Extensive Set of Cationic Lewis Acids.
Angew. Chem. Int. ed.2024, 63, e202403356.
www
16D. González-Pinardo, F. Krämer, F. Breher,* I. Fernández
Activation of s-Bonds by Group 13/Ylide-Based Ambiphiles: Understanding and Design.
Chem. Eur. J.2024, 2, e202400020.
www
15P. M. R. Wingering, F. Krämer, M. E. A. Dilanas, C. Ruiz-Martínez, I. Fernández, F. Breher
Structure and Solution Behaviour of Rare-Earth-Metal Complexes with Tripodal N-Donor Ligands.
Chem. Eur. J.2024, 30, e202400781.
www
14L. Köring, B. Birenheide, F. Krämer, J. O. Wenzel, R. Schoch, M. Brehm, F. Breher, J. Paradies
Synthesis of Ferrocenyl Boranes and their Application as Lewis Acids in Epoxide Rearrangements.
Eur. J. Inorg. Chem2024, 27, e202400057.
www
13F. Krämer, J. O. Wenzel, I. Fernández, F. Breher
Intramolecular dearomative 1,4-addition of silyl and germyl radicals to a phenyl moiety.
Dalton Trans Chem2024, 53, 2917-2921 .
www
12F. Krämer, J. Paradies, I. Fernández, F. Breher
Quo Vadis CO2 activation: Catalytic Reduction of CO2 to Methanol Using Aluminum and Gallium/Carbon-based Ambiphiles.
Chem. Eur. J.2024, 30, e202303380.
www
11F. Krämer, M. Leskov, F. Breher
The Solvent-free Lithium Alanate {Li[t-Bu2 AlH2 ]}n : A New Product Obtained from a Long-Known Reaction.
Eur. J. Inorg. Chem2024, 27, e202300561 .
www
10F. Krämer, J. Paradies, I. Fernández,* F. Breher
A crystalline aluminium/carbon-based ambiphile capable of activation and catalytic transfer of ammonia in aqueous media.
Nat. Chem.2024, 16, 63-69.
www
9P. M. R. Wingering, S. Hohnstein, F. Krämer, M. E. A. Dilanas, C. Ruiz-Martínez, I. Fernández, F. Breher
Synthesis, Crystal Structures, and Ion Pairing of K6N Complexes with Rare Earth Elements in the Solid State and in Solution.
Chem. Eur. J.2023, 29, e202301529.
www
8L. Köring, A. Stepen, B. Birenheide, S. Barth, M. Leskov, R. Schoch, F. Krämer, F. Breher, J. Paradies
Boron-Centered Lewis Superacid through Redox-Active Ligands: Application in C-F and S-F Bond Activation.
Angew. Chem.2023, 62, e202216959.
www
7L. Bayer, B. S. Birenheide, F. Krämer, S. Lebedkin, F. Breher 
Heterobimetallic Gold/Ruthenium Complexes Synthesized via Post-functionalisation and Applied in Dual Photoredox Gold Catalysis.
Chem. Eur. J.2022, 28, e202201856.
www
6F. Krämer, M. Radius, A. Hinz, M. E. A. Dilanas, F. Breher 
Accessing Cationic a-Silylated and a-Germylated Phosphorus Ylides.
Chem. Eur. J.2022, 28, e202103974.
www
5F. Krämer, M. Radius, H. Berberich, I. Fernández, F. Breher
A neutral, acyclic, borataalkene-like ligand for group 11 metals: L- and Z-type ligands side by side.
Chem. Commun.2022, 58, 3905-3908.
www
4F. Krämer, M. S. Luff, U. Radius, F. Weigend, F. Breher 
NON-Ligated N-Heterocyclic Tetrylenes.
Eur. J. Inorg. Chem.2021, 2021, 3591-3600.
www
3B. S. Birenheide, F. Krämer, L. Bayer, P. Mehlmann, F. Dielmann, F. Breher 
Multistimuli-Responsive [3] Dioxaphosphaferrocenophanes with Orthogonal Switches.
Chem. Eur. J.2021, 27, 15066-15073.
www
2T. P. Seifert, S. Bestgen, T. J. Feuerstein, S. Lebedkin, F. Krämer, C. Fengler, M. T. Gamer, M. M. Kappes, P. W. Roesky
Phosphine-substituted 1,2,3-triazoles as P,C- and P,N-ligands for photoluminescent coinage metal complexes.
Dalton Trans.2019, 48, 15427-15434.
www
1E. M. B. Moos, W. Feuerstein, F. Krämer, F. Breher
A Metal-Containing N-Heterocyclic Germylene Based on an Oxalamidine Framework.
Z. anorg. allg. Chem.2018, 644, 1115–1122.
www
Aktualisiert von: Sarah Matz