Michael Mastalerz

Professor

Ruprecht Karls Universität Heidelberg

Germany

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About

Michael Mastalerz is a Professor at Ruprecht Karls Universität Heidelberg in Germany. His research areas encompass materials science, specifically focusing on adsorption phenomena, supramolecular chemistry, and the synthesis of complex organic structures. Recent publications highlight his work on activated carbon adsorbents, the characterization of tetraazanonacenes, and novel methodologies for synthesizing chiral nanobelts.

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2022

Collaborators (3)

Jürgen H. Gross

Heidelberg University

GERMANY

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Jürgen Graf

Heidelberg University

GERMANY

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Wolfgang Wernsdorfer

Humboldt Professor

Karlsruher Institut für Technologie

GERMANY

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Michael Mastalerz

Research Interests

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About

Articles (23)

Characterization of the adsorption of H2 and N2 on activated carbon used as an adsorbent in cryosorption pumps

Oberflächengestützte Synthese und Charakterisierung von Tetraazanonacen

On‐Surface Synthesis and Characterization of Tetraazanonacene

C2-Symmetric Perylene-Embedded Double [5]Helicenes

Embedding a Planar Antiaromatic Cyclooctatetraene into a Truxene-Derived Polycyclic Aromatic Hydrocarbon

Dead Ends and Detours Towards a Rigid Hexasalicylic Aldehyde Precursor for Triptycene‐Based Porous Materials

Dead Ends and Detours Towards a Rigid Hexasalicylic Aldehyde Precursor for Triptycene‐Based Porous Materials

Supramolecular Interpenetrated Faujasite‐Like Crystals from [4+4] Imine Cages

High‐Yielding Nanobelt Formation by Chirality‐Assisted Synthesis

High‐Yielding Nanobelt Formation by Chirality‐Assisted Synthesis

Synthesis of Chiral Pyrene‐Based 1,4‐Dithiins

Synthesis of Chiral Pyrene‐Based 1,4‐Dithiins

Synthesis of a Benzotrisazulene via Trioxobenzotrisazulene

Palladium‐Catalyzed Cyclization of a Pyryne Precursor to Higher Pyrenylenes

Palladium‐Catalyzed Cyclization of a Pyryne Precursor to Higher Pyrenylenes

[4 + 4]-Imine Cage Compounds with Nitrogen-Rich Cavities and Tetrahedral Geometry

Solvent‐Controlled Quadruple Catenation of Giant Chiral [8+12] Salicylimine Cubes Driven by Weak Hydrogen Bonding

Solvent‐Controlled Quadruple Catenation of Giant Chiral [8+12] Salicylimine Cubes Driven by Weak Hydrogen Bonding

Dimeric and trimeric catenation of giant chiral [8 + 12] imine cubes driven by weak supramolecular interactions

Publisher Correction: Dimeric and trimeric catenation of giant chiral [8 + 12] imine cubes driven by weak supramolecular interactions

N‐Heterocyclic Carbene Mediated Sulfur Extrusion of Disulfides

Single Crystals of Insoluble Porous Salicylimine Cages

[2+3] Amide Cages by Oxidation of [2+3] Imine Cages – Revisiting Molecular Hosts for Highly Efficient Nitrate Binding

Collaborators (3)

Jürgen H. Gross

Jürgen Graf

Wolfgang Wernsdorfer

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