Litcius/Paper detail

Selective Transformation of Nickel‐Bound Formate to CO or C−C Coupling Products Triggered by Deprotonation and Steered by Alkali‐Metal Ions

Philipp Zimmermann, Deniz Ar, Marie Rößler, Patrick Holze, Beatrice Cula, Christian Herwig, Christian Limberg

2020Angewandte Chemie International Edition20 citationsDOIOpen Access PDF

Abstract

Abstract The complexes [L t Bu Ni(OCO‐ κ 2 O , C )]M 3 [N(SiMe 3 ) 2 ] 2 (M=Li, Na, K), synthesized by deprotonation of a nickel formate complex [L t Bu NiOOCH] with the corresponding amides M[N(SiMe 3 ) 2 ], feature a Ni II −CO 2 2− core surrounded by Lewis‐acidic cations (M + ) and the influence of the latter on the behavior and reactivity was studied. The results point to a decrease of CO 2 activation within the series Li, Na, and K, which is also reflected in the reactivity with Me 3 SiOTf leading to the liberation of CO and formation of a Ni−OSiMe 3 complex. Furthermore, in case of K + , the {[K 3 [N(SiMe 3 ) 2 ] 2 } + shell around the Ni−CO 2 2− entity was shown to have a large impact on its stabilization and behavior. If the number of K[N(SiMe 3 ) 2 ] equivalents used in the reaction with [L t Bu NiOOCH] is decreased from 3 to 0.5, the deprotonated part of the precursor enters a complex reaction sequence with formation of [L t Bu Ni I (μ‐OOCH)Ni I L t Bu ]K and [L t Bu Ni(C 2 O 4 )NiL t Bu ]. The same reaction at higher concentrations additionally led to the formation of a unique hexanuclear Ni II complex containing both oxalate and mesoxalate ([O 2 C‐CO 2 ‐CO 2 ] 4− ) ligands.

Topics & Concepts

DeprotonationChemistryReactivity (psychology)NickelFormateMedicinal chemistryOxalateMetalAlkali metalStereochemistryLigand (biochemistry)Inorganic chemistryIonCatalysisOrganic chemistryReceptorBiochemistryMedicinePathologyAlternative medicineCarbon dioxide utilization in catalysisCO2 Reduction Techniques and CatalystsCatalysis for Biomass Conversion