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New Routes to Rare Aromatic BN-Heterocycles: 1,3-Azaborinine and 1,3-Azaborolyl-Anion Derivatives

Subject Area Organic Molecular Chemistry - Synthesis and Characterisation
Term from 2020 to 2023
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 445827127
 
Final Report Year 2023

Final Report Abstract

With this project, we developed a viable new pathway to dihydro-1,3-azaborinine derivatives by means of multicomponent reactions between the reagents FmesBH2 borane, acetylene and isonitrile. New 1,3-azaborole derivatives were identified and isolated as intermediates in these sequences. Aryl substituted 1,3-azaborole systems showed interesting photophysical properties, namely aggregation-induced emission (AIE) upon H2O addition to their THF solutions. Deprotonation of the 1,3-azaboroles gave the respective cyclopentadienide analogous anions which were used as η5-ligands in Organometallic Chemistry (Rh, Ir). Eventually, treatment of the 1,3-azaborole derivatives with various isonitriles CN-R (R: xylyl, benzyl, -CH2CO2tBu) gave the corresponding 1,3-azaborinine derivatives. Variations of these multicomponent routes gave dihydro-1,3- azaborinine derived oxindole isosteres. Replacement of the alkyne component by nitriles opened pathway to 1,4,2-diazaborole derivatives and we could also employ various olefins as reagents in the FmesBH2/isonitrile utilizing multicomponent B/N heterocycle syntheses. We also investigated some reactivity of the FmesBH2 reagent toward a phosphanyl substituted alkyne which opened a pathway to a geminal P/B frustrated Lewis pair. The results were described in detail in six original publications.

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