M
Marc Ostermeier
Researcher at Humboldt University of Berlin
Publications - 6
Citations - 388
Marc Ostermeier is an academic researcher from Humboldt University of Berlin. The author has contributed to research in topics: Ligand & Piperazine. The author has an hindex of 6, co-authored 6 publications receiving 378 citations. Previous affiliations of Marc Ostermeier include Humboldt State University.
Papers
More filters
Journal ArticleDOI
Multifunctional “Clickates” as Versatile Extended Heteroaromatic Building Blocks: Efficient Synthesis via Click Chemistry, Conformational Preferences, and Metal Coordination
TL;DR: The extended heteroaromatic BTP scaffold should prove useful for the design of responsive foldamer backbones and the preparation of new magnetic and emissive materials.
Journal ArticleDOI
Complexes of Click-Derived Bistriazolylpyridines: Remarkable Electronic Influence of Remote Substituents on Thermodynamic Stability as well as Electronic and Magnetic Properties
Marc Ostermeier,Marie‐Anne Berlin,Robert M. Meudtner,Serhiy Demeshko,Franc Meyer,Christian Limberg,Stefan Hecht +6 more
TL;DR: The results nicely demonstrate the utility of substituent parameters, originally developed for linear free-energy relationships to explain reactivity in organic reactions, in coordination chemistry, and to illustrate the potential to custom-design btp ligands and complexes thereof with predictable properties.
Journal ArticleDOI
Solvent-dependent oxidation of a (pyridylmethyl)amino ligand by FeCl3 to give a water-soluble blue fluorophore.
Journal ArticleDOI
The Coordination Chemistry of Iron with the 1,4‐Bis(2‐pyridyl‐methyl)piperazine Ligand
TL;DR: In this article, the behavior of FeII and FeIII ions in combination with the potential ligand 1,4-bis(2-pyridyl-methyl)piperazine (BPMP) under anhydrous conditions has been investigated.
Journal ArticleDOI
Stabilizing the Boat Conformation of Piperazines Coordinated to Iron(II): iso-Butyl Substituents Lead to Robust Oxidation Catalysts via Hyperconjugation
TL;DR: In this paper, a chiral 2,5-di-iso-butyl-substituted 1,4-bis(2-pyridyl-methyl)piperazine was used as a ligand in metal complexes, and the most stable conformations of the free ligand contain the piperazine ring in a boat conformation with carbon atoms at the tips of the boat since repulsive interactions between the lone-pairs at the nitrogen atoms are avoided thereby.