Abstract

A facile synthetic route to Ni(0)(NHC)2 from stable Ni(II)(acac)2 was established without common but labile Ni(0) precursors. The intermediate is a divalent mono-NHC adduct of Ni(acac)2, Ni(NHC)(acac)2. Reduction of Ni(NHC)(acac)2 in both the presence and absence of an NHC ligand gave Ni(NHC)2 in ca. 90% and 40% conversions, respectively. Ni(NHC)2, especially with bis(2,6-diisopropylphenyl)imidazolin-2-ylidene, has strong Ni−C(carbene) bonds and remarkable anagostic Ni−H(methyl) interactions, stabilizing its 14e unsaturated structure.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.