Literature DB >> 29920807

Lewis-Base-Induced Disproportionation of a Dialane.

Alexander Hofmann1, Anna Lamprecht1, J Oscar C Jiménez-Halla2, Tobias Tröster1, Rian D Dewhurst1, Carsten Lenczyk1, Holger Braunschweig1.   

Abstract

The reaction of a pentamethylcyclopentadienyl-substituted dialane with a variety of Lewis bases results in unexpected disproportionation of the dialane into AlI and AlIII species. Use of a transition-metal Lewis base allows for the formation of metal-only Lewis pairs. Furthermore, the synthesis of a Lewis base bis-adduct was successful with the Lewis base 4-dimethylaminopyridine.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  Lewis base; aluminum; dialane; disproportionation; transition metals

Year:  2018        PMID: 29920807     DOI: 10.1002/chem.201802300

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  4 in total

1.  Monomeric Cp3tAl(i): synthesis, reactivity, and the concept of valence isomerism.

Authors:  Alexander Hofmann; Tobias Tröster; Thomas Kupfer; Holger Braunschweig
Journal:  Chem Sci       Date:  2019-01-14       Impact factor: 9.825

2.  Donor-Stabilized Monocarba-Bridged Bis(cyclopentadienyl)alanes.

Authors:  Wasim Haider; Volker Huch; Bernd Morgenstern; André Schäfer
Journal:  ChemistryOpen       Date:  2020-09-23       Impact factor: 2.630

3.  Planar Cyclopenten-4-yl Cations: Highly Delocalized π Aromatics Stabilized by Hyperconjugation.

Authors:  Samuel Nees; Thomas Kupfer; Alexander Hofmann; Holger Braunschweig
Journal:  Angew Chem Int Ed Engl       Date:  2020-08-25       Impact factor: 16.823

4.  Reversible Reductive Elimination in Aluminum(II) Dihydrides.

Authors:  Rosalyn L Falconer; Gary S Nichol; Ivan V Smolyar; Scott L Cockroft; Michael J Cowley
Journal:  Angew Chem Int Ed Engl       Date:  2020-11-24       Impact factor: 15.336

  4 in total

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