Carbene transfer reactivity from a nickelacyclobutane

Publication date

2024-11-04

Authors

Sansores Paredes, MaríaISNI 000000050730969X
Lutz, M.ORCID 0000-0003-1524-9629ISNI 0000000352600916
Moret, Marc EtienneORCID 0000-0002-3137-6073ISNI 0000000436414547

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Advisors

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Document Type

Article
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License

cc_by

Abstract

A formal carbene-transfer reaction from an isolated nickelacyclobutane to an isocyanide to form a ketenimine is reported. DFT calculations support a stepwise 1,1-insertion/fragmentation pathway without a carbene intermediate. This unusual reactivity suggests a potential new role as “carbene reservoir” for nickelacyclobutanes, which are typically seen as intermediates in catalytic cyclopropanation.

Keywords

Electronic, Optical and Magnetic Materials, Catalysis, Ceramics and Composites, General Chemistry, Surfaces, Coatings and Films, Metals and Alloys, Materials Chemistry

Citation

Sansores-Paredes, M L G, Lutz, M & Moret, M E 2024, 'Carbene transfer reactivity from a nickelacyclobutane', Chemical Communications, vol. 60, no. 85, pp. 12397-12400. https://doi.org/10.1039/d4cc04273e