Zincocene and Dizincocene N‐Heterocyclic Carbene Complexes and Catalytic Hydrogenation of Imines and Ketones

Jochmann, Phillip; Stephan, Douglas W.

doi:10.1002/chem.201402875

Cited by 57 publications

(18 citation statements)

References 92 publications

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“…While several main group metals exhibit activity for imine hydrogenation, homogeneous ketone hydrogenation by main group metals is exceptionally limited. The reported examples involve extremely high pressures, 58 , 60 , 61 the use of additives, 62 or a narrow substrate scope. 58 , 60 , 63 Thus, it is significant that we found that 1 can catalyze the hydrogenation of ketones with aromatic, aliphatic, and mixed aromatic/aliphatic R and R′ substituents under 65 bar of H 2 at 140 °C.…”

Section: Resultsmentioning

confidence: 99%

Metal–Ligand Cooperation Facilitates Bond Activation and Catalytic Hydrogenation with Zinc Pincer Complexes

et al. 2020

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A series of PNP zinc pincer complexes capable of bond activation via aromatization/dearomatization metal–ligand cooperation (MLC) were prepared and characterized. Reversible heterolytic N–H and H–H bond activation by MLC is shown, in which hemilability of the phosphorus linkers plays a key role. Utilizing this zinc pincer system, base-free catalytic hydrogenation of imines and ketones is demonstrated. A detailed mechanistic study supported by computation implicates the key role of MLC in facilitating effective catalysis. This approach offers a new strategy for (de)hydrogenation and other catalytic transformations mediated by zinc and other main group metals.

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Section: Resultsmentioning

confidence: 99%

Metal–Ligand Cooperation Facilitates Bond Activation and Catalytic Hydrogenation with Zinc Pincer Complexes

et al. 2020

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“…16 The dialkoxide adducts [(IDipp)Zn(OCHR 2 ) 2 ] (25, R = Ph, t-Bu) were produced by hydrogenation of [ZnCp* 2 ] (4 bar H 2 ) in the presence of R 2 C=O and IDipp. 33 Alternatively, protonolysis of [ZnCp* 2 ] with R 2 CHOH (R = Ph, t-Bu; 2 equiv) and subsequent addition of IDipp also allowed the…”

Section: Scheme 15 Co 2 Hydrosilylation Catalysis Mediated By Zn-h Camentioning

confidence: 99%

Recent Developments on N-Heterocyclic Carbene Supported Zinc Complexes: Synthesis and Use in Catalysis

Dagorne

2018

Synthesis

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The present contribution reviews the synthesis, reactivity, and use in catalysis of NHC–Zn complexes reported since 2013. NHC-stabilized Zn(II) species typically display enhanced stability relative to common organozinc species (such as Zn dialkyls), a feature of interest for the mediation of various chemical processes and the stabilization of reactive Zn-based species. Their use in catalysis is essentially dominated by reduction reactions of various unsaturated small molecules (including CO2), thus primarily involving Zn–H and Zn–alkyl derivatives as catalysts. Simple NHC adducts of Zn(II) dihalides also appear as effective catalysts for the reduction amination of CO2 and borylation of alkyl/aryl halides. Stable and well-defined Zn alkoxides have also been prepared and behave as effective catalysts in the polymerization of cyclic esters/carbonates for the production of well-defined biodegradable materials. Overall, the attractive features of NHC-based Zn(II) species include ready access, a reasonable stability/reactivity balance, and steric/electronic tunability (through the NHC source), which should promote their further development.1 Introduction2 NHC-Supported Zinc Alkyl/Aryl Species2.1 Synthesis2.2 Reactivity and Use in Catalysis3 NHC-Supported Zinc Hydride Species3.1 Synthesis3.2 Reactivity and Use in Catalysis4 NHC-Supported Zinc Amido/Alkoxide Species4.1 Synthesis4.2 Use in Catalysis5 NHC-Supported Zinc Dihalide Species5.1 Synthesis5.2 Use in Catalysis6 Other NHC-Stabilized Zn Species7 Conclusion

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“…The aluminium hydride compound (iso-butyl) 2 AlH is an odd example of a main group metal catalyst that can be used, but needs harsh conditions (100 bar H 2 , 100 °C, 24 h) 27 . Recently, a zinc hydride catalyst was introduced but similarly high pressures need to be applied (70-100 bar) 28,29 . Figure 2b shows metal-free organocatalysts.…”

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confidence: 99%

Imine hydrogenation with simple alkaline earth metal catalysts

et al. 2018

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W ith molecular hydrogen being one of the cleanest reducing agents, catalytic hydrogenation using the more noble transition metals is among the most studied of all chemical processes 1 . Increasing social pressure towards a sustainable society, however, dictates replacement of costly, and often harmful, precious metals by more abundant first-row transition metals or even biocompatible redox inactive main group metals [2][3][4][5][6] . The alkaline earth metal calcium does not possess partially filled d orbitals for substrate activation, but has recently shown catalytic activities in the hydrogenation of C= C double bonds with molecular H 2 (ref. 7 ). Although restricted to conjugated C= C bonds, this example strikingly broke the dogma that transition metals are needed for alkene hydrogenation. This was followed by the development of metal-free frustrated Lewis pair (FLP) catalysts [8][9][10][11] and, most recently, cationic calcium hydride catalysts that are also able to hydrogenate unactivated alkenes 12 . Figure 1a shows a working hypothesis for styrene hydrogenation with a dibenzylcalcium catalyst (CaBn 2 ) 7 . The first step is the generation of a calcium hydride species, for which ample precedence exists [13][14][15][16][17] . Further reaction with H 2 may cause precipitation of insoluble (CaH 2 ) n , but catalyst loss is partly prevented by aggregation to soluble but undefined Ca x Bn y H z species. Despite a lack of d orbitals, alkene activation proceeds through a weak electrostatic calciumalkene interaction, recently shown to be of importance in calcium catalysis 18 . The benzylic calcium intermediate formed after insertion may, after successive styrene insertions, form polystyrene 19 , but high H 2 pressure (20-100 bar) can prevent this side reaction by promoting σ-bond metathesis. The latter step in the cycle is, like the initiation reaction, formally a deprotonation of H 2 by a resonance-stabilized benzylic carbanion. Considering the high pK a of H 2 (≈ 49) 20 , this reaction seemed questionable. Stoichiometric conversions of model systems, however, underscored the feasibility of this pathway 7 . Independent theoretical calculations illustrate that the final σ-bond metathesis step is indeed highly endergonic: Gibbs free energy of activation Δ G ‡ (60 °C, 20 bar) = 25.7 kcal mol −1 (ref. 21 ).As the highly atom-efficient catalytic reduction of imines by H 2 received much less attention than alkene or ketone hydrogenation [22][23][24] , it remained an important question whether calcium-catalysed hydrogenation can be extended to imine reduction. Current stateof-the-art imine hydrogenation catalysts can be divided into four categories that vary in terms of substrate activation and nucleophilic power ( Fig. 2a-d). Figure 2a shows organometallic metal hydrides that rely on hydride nucleophilicity. Apart from few early transition metal catalysts (Ti 25 , lanthanides 26 ), these are generally based on late transition metals (Rh, Ir) 22 . The aluminium hydride compound (iso-butyl) 2 AlH is an odd example of a ...

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Zincocene and Dizincocene N‐Heterocyclic Carbene Complexes and Catalytic Hydrogenation of Imines and Ketones

Cited by 57 publications

References 92 publications

Metal–Ligand Cooperation Facilitates Bond Activation and Catalytic Hydrogenation with Zinc Pincer Complexes

Metal–Ligand Cooperation Facilitates Bond Activation and Catalytic Hydrogenation with Zinc Pincer Complexes

Recent Developments on N-Heterocyclic Carbene Supported Zinc Complexes: Synthesis and Use in Catalysis

Imine hydrogenation with simple alkaline earth metal catalysts

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