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Adrian-Mihail Stadler

Researcher at Karlsruhe Institute of Technology

Publications -  36
Citations -  1206

Adrian-Mihail Stadler is an academic researcher from Karlsruhe Institute of Technology. The author has contributed to research in topics: Ligand & Supramolecular chemistry. The author has an hindex of 19, co-authored 36 publications receiving 1130 citations. Previous affiliations of Adrian-Mihail Stadler include Centre national de la recherche scientifique & University of Strasbourg.

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Bis-acyl-/aroyl-hydrazones as multidentate ligands

TL;DR: Bis-acyl-/aroyl-hydrazones can be divided into two basic structural categories: those derived from a dihydrazide and those that are derived from dialdehyde (or diketone).
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Formation of RACK- and grid-type metallosupramolecular architectures and generation of molecular motion by reversible uncoiling of helical ligand strands.

TL;DR: The interaction of appropriate metal ions with helical ligand strands, obtained by hydrazone polycondensation, generates polymetallic supramolecular architectures of rack and grid types, by uncoiling of the ligand.
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Contraction/extension molecular motion by protonation/deprotonation induced structural switching of pyridine derived oligoamides

TL;DR: NMR, mass spectrometry and X-ray diffraction studies show reversible structural interconversion between helical and extended forms of pyridine derived oligoamide molecular strands, by simple protonation/deprotonation.
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Solid‐State Self‐Assembly of Polymeric Double Helicates Leading to Linear Arrays of Silver(I) Ions and Reversible Strand/Double Helix Interconversion in Solution

TL;DR: Progressive addition of silver(I) ions to a 1:1 mixture of 1 and 5 leads to the preferential formation of the double helicate 2 over the grid complex 6, illustrating a process of self-organisation with selection of the correct ligand.
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Synthesis, structural features, absorption spectra, redox behaviour and luminescence properties of ruthenium(ii) rack-type dinuclear complexes with ditopic, hydrazone-based ligands

TL;DR: The results clearly indicate that the structural variations introduced translate into interesting differences in the spectroscopic, luminescence and redox properties of the ligand strands as well as of the rack-type metal complexes.