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Projekt Druckansicht

Elektronenreiches, monovalentes Bor: eine Plattform für metallähnliche Reaktivitäten

Fachliche Zuordnung Anorganische Molekülchemie - Synthese, Charakterisierung
Förderung Förderung von 2017 bis 2020
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 325229020
 
Erstellungsjahr 2020

Zusammenfassung der Projektergebnisse

This project has opened up huge opportunities for future research in our group. The TM-borylene chemistry, upon which the original proposal was based, has seen a large expansion of promising TM-borylene reagents, as well as a number of new modes of liberation of the borylene ligand using Lewis bases and other reagents such as chalcogens, leading to new (metal-free) monovalent boron compounds, iminoboranes as well as a number of new classes of boron-containing heterocycles. The metal-free chemistry of monovalent boron compounds, a more recent offshoot of this chemistry, has already witnessed some major breakthroughs such as the first fixation, reduction and dimerization of N2 at a main-group atom, and ultimately the confirmed one-pot synthesis of ammonium from N2 using this system. A huge number of possibilities beckon from these results in different directions, namely: (a) the use of monovalent boron species in the activation of other challenging small molecules, and (b) the development of the N2 fixation chemistry towards practical methods to prepare ammonia and other value-added nitrogencontaining compounds.

Projektbezogene Publikationen (Auswahl)

  • Synthesis and Trapping of Iminoboranes via M=B/C=N Bond Metathesis, Angew. Chem. Int. Ed. 2017, 56, 7975–7979
    B. Borthakur, H. Braunschweig, A. Deißenberger, T. Dellermann, R. D. Dewhurst, I. Krummenacher, M. Nutz, A. K. Phukan, M. Schäfer
    (Siehe online unter https://doi.org/10.1002/anie.201703324)
  • The First Boron-Tellurium Double Bond: Direct Insertion of Heavy Chalcogens into a Mn=B Double Bond, Angew. Chem. Int. Ed. 2017, 56, 15760–15763
    S. Liu, M.-A. Légaré, D. Auerhammer, A. Hofmann, H. Braunschweig
    (Siehe online unter https://doi.org/10.1002/anie.201708729)
  • A Boradiselenirane and a Boraditellurirane: Isolable Heavy Analogs of Dioxiranes and Dithiiranes, J. Am. Chem. Soc. 2018, 140, 11223–11226
    S. Liu, M.-A. Légaré, A. Hofmann, H. Braunschweig
    (Siehe online unter https://doi.org/10.1021/jacs.8b07829)
  • Nitrogen fixation and reduction at boron, Science 2018, 359, 896–900
    M.-A. Légaré, G. Bélanger-Chabot, R. D. Dewhurst, E. Welz, I. Krummenacher, B. Engels, H. Braunschweig
    (Siehe online unter https://doi.org/10.1126/science.aaq1684)
  • Release of Isonitrile- and NHC-stabilized Borylenes from Group VI Terminal Borylene Complexes, Chem. Eur. J. 2018, 24, 6843–6847
    M. Nutz, B. Borthakur, C. Pranckevicius, R. D. Dewhurst, M. Schäfer, T. Dellermann, F. Glaab, M. Thaler, A. K. Phukan, H. Braunschweig
    (Siehe online unter https://doi.org/10.1002/chem.201800593)
  • Boron: Its role in energy related research and applications, Angew. Chem. Int. Ed.
    Z. Huang, S. Wang, R. D. Dewhurst, N. V. Ignat'ev, M. Finze, H. Braunschweig
    (Siehe online unter https://doi.org/10.1002/anie.201911108)
  • Metallomimetic Chemistry of Boron, Chem. Rev. 2019, 119, 8231–8261
    M.-A. Légaré, C. Pranckevicius, H. Braunschweig
    (Siehe online unter https://doi.org/10.1021/acs.chemrev.8b00561)
  • Recent Advances in Boron-Centered Ligands and Their Transition Metal Complexes, Coord. Chem. Rev. 2019, 184–200
    J. T. Goettel, H. Braunschweig
    (Siehe online unter https://doi.org/10.1016/j.ccr.2018.09.013)
  • Synthesis of unsymmetrical B2E2 and B2E3 heterocycles by borylene insertion into boradichalcogeniranes, Chem. Sci. 2019, 10, 4662–4666
    S. Liu, M.-A. Légaré, A. Hofmann, A. Rempel, S. Hagspiel, H. Braunschweig
    (Siehe online unter https://doi.org/10.1039/c9sc00657e)
  • The reductive coupling of dinitrogen, Science 2019, 363, 1329–1332
    M.-A. Légaré, M. Rang, G. Bélanger-Chabot, J. I. Schweizer, I. Krummenacher, R. Bertermann, M. Arrowsmith, M. C. Holthausen, H. Braunschweig
    (Siehe online unter https://doi.org/10.1126/science.aav9593)
 
 

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