Abstract
[1+2] cycloaddition between a cyclic (alkyl)(amino)aluminyl anion (3) and diaryldiazomethane affords an AlN2 three-membered ring species (4). Compound (4) is thermally unstable and spontaneously releases N2 gas under the mild reaction condition to generate an ion-separated species 5. An X-ray study shows that the anionic part of 5 bears a considerable short exocyclic Al−C bond, and computational studies involving molecular orbital and natural bond orbital analysis indicate the Al=C π bonding character. The Al=C moiety of 5 undergoes intramolecular C−H activation. Moreover, reaction of 5 with a diazo compound leads to the reduction and complete cleavage of the N=N double bond.
Original language | English |
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Article number | e202211800 |
Journal | Angewandte Chemie - International Edition |
Volume | 61 |
Issue number | 42 |
DOIs | |
Publication status | Published - Oct 17 2022 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2022 Wiley-VCH GmbH.
ASJC Scopus Subject Areas
- Catalysis
- General Chemistry
Keywords
- Aluminyl Anion
- Bond Cleavage
- C−H Activation
- Diazirine
- π Bonding