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Updated: Nov 22, 2025

Synthesis and Purification of Iodoaziridines Involving Quantitative Selection of the Optimal Stationary Phase for Chromatography
Published on: May 16, 2014
Aryl-substituted triarsiranes: synthesis and reactivity
André Schumann1, Jonas Bresien2, Malte Fischer1
1Leibniz Institut für Katalyse e.V. (LIKAT), A.-Einstein-Str.3a, 18059 Rostock, Germany. christian.hering-junghans@catalysis.de.
Researchers developed a scalable synthesis for cyclotriarsanes, enabling studies on their reactivity. This led to new titanocene diarsene complexes and N-heterocyclic carbene-arsinidene adducts.
Area of Science:
- Organometallic Chemistry
- Main Group Chemistry
Background:
- Cyclotriarsanes, compounds featuring a three-membered ring of arsenic atoms, are uncommon in chemical literature.
- Exploring the synthesis and reactivity of novel arsenic clusters is crucial for advancing inorganic chemistry.
Purpose of the Study:
- To establish a scalable synthetic route for cyclotriarsanes.
- To investigate the reactivity of cyclotriarsanes with titanocene complexes and N-heterocyclic carbenes (NHCs).
Main Methods:
- Development of a scalable synthetic protocol for cyclotriarsane ((AsAr)3) synthesis.
- Reaction of the synthesized cyclotriarsane with [Cp2Ti(C2(SiMe3)2)] to form titanocene complexes.
- Reaction of the synthesized cyclotriarsane with N-heterocyclic carbenes (NHCs).
Main Results:
- A scalable synthetic method for cyclotriarsanes was successfully established.
- The reactivity studies yielded novel titanocene diarsene complexes.
- A variety of N-heterocyclic carbene-arsinidene adducts were synthesized through straightforward reactions.
Conclusions:
- The developed synthetic protocol provides accessible cyclotriarsanes for further chemical exploration.
- Cyclotriarsanes exhibit versatile reactivity, leading to the formation of unique organometallic and coordination compounds.
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