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Anzahl der Publikationen: 8
Zeitschriftenartikel
Born, Max; Karaghiosoff, Konstantin; Klapötke, Thomas M. und Voggenreiter, Michael
(2022):
Oxetane Monomers Based On the Powerful Explosive LLM-116: Improved Performance, Insensitivity, and Thermostability.
In: Chempluschem, Bd. 87, Nr. 3
[PDF, 7MB]
Born, Max; Karaghiosoff, Konstantin und Klapötke, Thomas M.
(2022):
Improved Preparation of 3-Oximinooxetane - An Important Precursor to Energetic Oxetanes.
In: Propellants Explosives Pyrotechnics, Bd. 47, Nr. 3
[PDF, 727kB]
Born, Max; Plank, Jakob und Klapötke, Thomas M.
(2022):
Energetic Polymers: A Chance for Lightweight Reactive Structure Materials?
In: Propellants Explosives Pyrotechnics, Bd. 47, Nr. 4
[PDF, 635kB]
Born, Max; Fessard, Thomas C.; Göttemann, Lucas; Karaghiosoff, Konstantin; Plank, Jakob und Klapötke, Thomas M.
(2022):
3-(Nitromethylene)oxetane: a very versatile and promising building block for energetic oxetane based monomers.
In: Materials Advances, Bd. 3, Nr. 8: S. 3479-3489
[PDF, 5MB]
Born, Max; Fessard, Thomas C.; Goettemann, Lucas; Plank, Jakob und Klapoetke, Thomas M.
(2022):
A GAP Replacement, Part 2: Preparation of Poly(3-azidooxetane) via Azidation of Poly(3-tosyloxyoxetane) and Poly(3-mesyloxyoxetane).
In: Journal of Organic Chemistry, Bd. 87, Nr. 6: S. 4097-4106
Born, Max; Fessard, Thomas C.; Göttemann, Lucas; Klapötke, Thomas M.; Stierstorfer, Jorg und Voggenreiter, Michael
(2021):
3,3-Dinitratooxetane - an important leap towards energetic oxygen-rich monomers and polymers.
In: Chemical Communications, Bd. 57, Nr. 22: S. 2804-2807
Born, Max; Karaghiosoff, Konstantin und Klapötke, Thomas M.
(2021):
A GAP Replacement: Improved Synthesis of 3-Azidooxetane and Its Homopolymer Based on Sulfonic Acid Esters of Oxetan-3-ol.
In: Journal of Organic Chemistry, Bd. 86, Nr. 18: S. 12607-12614
Dosch, Dominik E.; Reichel, Marco; Born, Max; Klapötke, Thomas M. und Karaghiosoff, Konstantin
(2021):
Investigation of Structure-Property Relationships of Three Nitroaromatic Compounds: 1-Fluoro-2,4,6-trinitrobenzene, 2,4,6-Trinitrophenyl Methanesulfonate, and 2,4,6-Trinitrobenzaldehyde.
In: Crystal Growth & Design, Bd. 21, Nr. 1: S. 243-248