Abstract

A comprehensive study on the synthesis and characterization of NHC-ligated nickel(II) cyanoborates (CBs) is presented (NHC = N-heterocyclic carbene). Nickel(II) cyanoborates Ni[BH2(CN)2]2·H2O (Ib·H2O), Ni[BH(CN)3]2·0.5H2O (Ic·0.5H2O), Ni[B(CN)4]2·H2O (Id·H2O) were reacted with selected NHCs of different steric size. The reaction of the nickel cyanoborates with small to medium-sized NHCs Me2ImMe and iPr2Im (R2Im = 1,3-di-organyl-imidazolin-2-ylidene; R2ImMe = 1,3-di-organyl-4,5-dimethyl-imidazolin-2-ylidene) afforded cyanoborate salts containing the rare homoleptic fourfold NHC-ligated nickel(II) cations [Ni(NHC)4]2+ (NHC = Me2ImMe (1c-d), iPr2Im (2c-d)) and cyanoborate counter-anions. Bulkier NHCs such as Mes2Im and Dipp2Im afforded complexes trans-[Ni(NHC)2(CB)2] (trans-4b, trans-5c). For the combination of the cyanoborate anion [BH2(CN)2]- and iPr2ImMe the salt of the tris-NHC complex [Ni(iPr2ImMe)3(NC-BH2CN)][BH2(CN)2] (3b) was isolated. Salt metathesis of NHC-ligated nickel(II) halides (Ni(NHC)2X2) (X = Cl, Br) with silver(I) and alkali metal cyanoborates were used to synthesize mono- and disubstituted coordination compounds of the type cis- or trans-[Ni(NHC)2(CB)X] (cis-10c, cis-11c, trans-12b) and cis- or trans-[Ni(NHC)2(CB)2] (cis-13b, cis-14a-c, trans-14a-b, trans-15b, trans-5b). Further investigations reveal that NHC-ligated cyanoborate complexes can act as building blocks for coordination polymers, as observed for structurally characterized 1∞{trans-[Ni(Mes2Im)2(μ2-[NC-BH2-CN])2]·2Ag(μ2-[BH2(CN)2])} (trans-5b·Ag). This study demonstrates the diverse character of cyanoborates in coordination chemistry as both, non-coordinating counter-anions, and weakly to medium coordinating anions forming novel transition metal complexes and salts. It provides evidence that a proper choice of cyanoborate and a proper choice of co-ligand can lead to a rich coordination chemistry of cyanoborate anions.

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