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Andreas Gebauer

Researcher at University of Texas at Austin

Publications -  21
Citations -  465

Andreas Gebauer is an academic researcher from University of Texas at Austin. The author has contributed to research in topics: Ferrocene & Porphyrin. The author has an hindex of 13, co-authored 21 publications receiving 451 citations. Previous affiliations of Andreas Gebauer include Lawrence Berkeley National Laboratory & University of Texas System.

Papers
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Journal ArticleDOI

Actinide expanded porphyrin complexes

TL;DR: In this paper, the UO22+ coordination chemistry of several prototypic expanded porphyrins is reviewed, and the ability of these expanded polypyrrolic ligands to stabilize complexes containing the uranyl cation is contrasted to that of the porphrin system.
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Metal Complexes of Porphycene, Corrphycene, and Hemiporphycene: Stability and Coordination Chemistry

TL;DR: Differences in electronic structure and nitrogen-core size in the free-base forms of these four systems are reflected in the properties of their corresponding metal complexes, and it is shown that for the zinc, magnesium, and cobalt complexes, there are distinct differences in the ability to maintain four-, five-, or six-coordinate geometries in the presence of similar concentrations of pyridine.
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Synthesis and Characterization of All-Alkyl-Substituted Mono-, Di-, and Trioxosapphyrins

TL;DR: In this article, the synthesis and characterization of the following heterosapphyrins is presented: 3,7,18,22-tetraethyl-2,8,12,13,17,23-hexamethyl-27-oxasapphynin (5), 3, 8, 12, 13, 17, 22-hexaethyl -2,7-18, 23tetramethyl-15,29-dioxasapphrin (6), and 3, 7, 18, 22 -tetrasapphrynin
Patent

Calixpyrroles, calixpyridinopyrroles and calixpyridines

TL;DR: In this paper, the calixpyrrole, calix pyridinopyrrole and calix polygonal porphyrinogen macrocycles are presented.
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Self-Assembly of Pyrrole–Ferrocene Hybrids, Determined Inter Alia by a New Chemically Induced Electrospray Mass Spectrometry Technique

TL;DR: An interesting example of a noncovalently linked organometallic superstructure is obtained from the self-assembly of tetrapyrrole-substituted ferrocene as mentioned in this paper.