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Projekt Druckansicht

Metallvermittelte Cyclisierung von Iminoboranen: Metallorganische Chemie und funktionelle BN-Isostere

Fachliche Zuordnung Anorganische Molekülchemie - Synthese, Charakterisierung
Förderung Förderung von 2013 bis 2021
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 238305216
 
Erstellungsjahr 2021

Zusammenfassung der Projektergebnisse

The majority of the results of this project concern either the expansion of the family of 1,2-azaborinines and the exploration of reactivity of rhodium 1,2-azaborete complexes, about which little was previously known. In both regards, a large body of new compounds and reactions were uncovered, leading to the publication of three original research articles in top journals. The somewhat temperamental synthesis of 1,2-azaborinines from rhodium 1,2-azaborete complexes hampered our efforts to install more exotic, functional units into these heterocyclic species. However, the aforementioned discovery of a new route to 1,2-azaborinines using the more reactive 1-rhoda-3,2-azaborole complexes, which appears to allow reaction with more bulky alkyne components, gives us hope that the construction of a wider range of heterocycles may be possible in future work. These possibilities are currently under investigation in our laboratories. A number of research results remain to be published, including a range of novel reactions of rhodium 1,2-azaborete complexes and 1-rhoda-3,2-azaborole complexes (e.g. with HCl, azides, pyridines, isocyanides and carbodiimides). A particular highlight is the reaction of a 1-rhoda-3,2-azaborole complex with an iminoborane, leading to the first known example of a 1,3-diaza-2,4-diborinine, with a C2B2N2 core and alternating B-N-B-N connectivity. These results require further investigation. Overall, although the azaborinine heterocycles were initially our major focus in this project, the surprisingly reactive rhodium-containing intermediate may turn out to be the true stars of the show: they have already demonstrated a fascinating diversity of reactions, and we have high hopes for their future chemistry.

Projektbezogene Publikationen (Auswahl)

 
 

Zusatzinformationen

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