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Projekt Druckansicht

Stark elektrophile Borenium-Ionen zur Aktivierung kleiner Moleküle

Fachliche Zuordnung Organische Molekülchemie - Synthese, Charakterisierung
Anorganische Molekülchemie - Synthese, Charakterisierung
Förderung Förderung von 2020 bis 2024
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 447833148
 
Erstellungsjahr 2023

Zusammenfassung der Projektergebnisse

Hydride abstraction from N-heterocyclic carbene adducts of pentafluorophenylborane gave the [(NHC)BH(C6F5)]+ borenium cations, which served as the central compounds of our study. They gave stable borane carbonyls upon exposure to carbon monoxide. Insertion of elemental sulfur into the B-H bond followed by deprotonation gave NHC stabilized thioxoboranes. Thermolysis of the [(IPr)BH(C6F5)]+ borenium featuring isopropyl substituents at the NHC nitrogen atoms resulted in C-H activation with loss of dihydrogen. Subsequent deprotonation of the newly formed cyclic borenium system gave the respective acyclic boraalkene. Its reactions were intensively investigated. This included several examples of formal [2+2]cycloaddition reactions, but also chalcogena-borirane formation upon treatment with elemental sulfur or selenium, oxidation with dinitrogenmonoxide and nitroxide radical formation upon treatment with nitrosobenzene. Starting from our parent BH-borenium systems a short synthetic pathway led to the formation of the neutral acyclic NHC stabilized B=CH2 boraalkene examples, whose chemistry was characterized experimentally. Related C-substituted boraalkenes were obtained from a closely related preparation sequence that involved an initial alkene hydroboration reaction. A similar boraalkene example was prepared that contained the linear isothiocyanate substituent at boron instead of the ubiquitous fluorinated aryls. The acyclic boraalkene examples underwent an unusual reaction with carbon disulfide that resulted in the cleavage of the B=C linkage. Some of the newly formed acyclic boraalkenes were used as pi-ligands in metal coordination chemistry.

Projektbezogene Publikationen (Auswahl)

 
 

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