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Lewis-Base-Induced Disproportionation of a Dialane.

Authors :
Hofmann A
Lamprecht A
Jiménez-Halla JOC
Tröster T
Dewhurst RD
Lenczyk C
Braunschweig H
Source :
Chemistry (Weinheim an der Bergstrasse, Germany) [Chemistry] 2018 Aug 09; Vol. 24 (45), pp. 11795-11802. Date of Electronic Publication: 2018 Jul 18.
Publication Year :
2018

Abstract

The reaction of a pentamethylcyclopentadienyl-substituted dialane with a variety of Lewis bases results in unexpected disproportionation of the dialane into Al <superscript>I</superscript> and Al <superscript>III</superscript> 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.<br /> (© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Details

Language :
English
ISSN :
1521-3765
Volume :
24
Issue :
45
Database :
MEDLINE
Journal :
Chemistry (Weinheim an der Bergstrasse, Germany)
Publication Type :
Academic Journal
Accession number :
29920807
Full Text :
https://doi.org/10.1002/chem.201802300