Abstract

Strongly Lewis acidic cationic aluminium complexes, stabilized by β–diketiminate (BDI) ligands and free of Lewis bases, have been prepared as their B(C6F5)4 − salts and were investigated for catalytic activity in imine hydrogenation. The backbone (R1) and N (R2) substituents on the R1,R2BDI ligand (R1,R2BDI=HC[C(R1)N(R2)]2) influence sterics and Lewis acidity. Ligand bulk increases along the row Me,DIPPBDI<Me,DIPePBDI≈tBu,DIPPBDI<tBu,DIPePBDI; DIPP=2,6‐C(H)Me2‐phenyl, DIPeP=2,6‐C(H)Et2‐phenyl. The Gutmann‐Beckett test showed acceptor numbers of: (tBu,DIPPBDI)AlMe+ 85.6, (tBu,DIPePBDI)AlMe+ 85.9, (Me,DIPPBDI)AlMe+ 89.7, (Me,DIPePBDI)AlMe+ 90.8, (Me,DIPPBDI)AlH+ 95.3. Steric and electronic factors need to be balanced for catalytic activity in imine hydrogenation. Open, highly Lewis acidic, cations strongly coordinate imine rendering it inactive as a Frustrated Lewis Pair (FLP). The bulkiest cations do not coordinate imine but its combination is also not an active catalyst. The cation (tBu,DIPPBDI)AlMe+ shows the best catalytic activity for various imines and is also an active catalyst for the Tishchenko reaction of benzaldehyde to benzylbenzoate. DFT calculations on the mechanism of imine hydrogenation catalysed by cationic Al complexes reveal two interconnected catalytic cycles operating in concert. Hydrogen is activated either by FLP reactivity of an Al⋅⋅⋅imine couple or, after formation of significant quantities of amine, by reaction with an Al⋅⋅⋅amine couple. The latter autocatalytic Al⋅⋅⋅amine cycle is energetically favoured.

Highlights

  • Lewis acids are frequently used as highly robust catalysts in many industrial applications.[1]

  • We recently reported that Jordan’s cationic β-diketiminate aluminium complex, (Me,DIPPBDI)AlMe+, can be used as a highly Lewis acidic component in Frustrated Lewis Pair (FLP) activation of alkynes or CO2.[20]. Attempts to convert these stoichiometric reactions to a catalytic protocol failed

  • While it is known that neutral Al compounds like AliBu3 catalyse this reaction under harsh conditions (> 100 bar H2, 100 °C)[32] and LiAlH4 is an effective catalyst under relatively mild conditions (1 bar, 80 °C),[33,34] we report a series of highly Lewis acidic cationic β-diketiminate (BDI) Al catalysts

Read more

Summary

Introduction

Lewis acids are frequently used as highly robust catalysts in many industrial applications.[1]. (b) General catalytic cycle for imine hydrogenation by a Lewis acid. Like in the previously reported structures of (Me,DIPPBDI)AlMe2 and (Me,DIPPBDI)AlH2,[36,37] the (BDI)AlR2 complexes exhibit Al centres www.chemeurj.org

Results
Conclusion

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.