4.7 Article

Selective dimerization of α-methylstyrene by tunable bis(catecholato)germane Lewis acid catalysts

Journal

DALTON TRANSACTIONS
Volume 50, Issue 43, Pages 15906-15913

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1dt03180e

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Funding

  1. Natural Sciences and Engineering Research Council of Canada (NSERC)
  2. University of Western Ontario
  3. Alexander von Humboldt Foundation

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This study reports the synthesis of various bis(catecholato)germanes and their application in catalysis. The Lewis acidity of these compounds was evaluated using experimental and computational methods, and the addition of donor additives in the dimerization reaction showed comparable selectivity control to transition metal catalyst systems.
The synthesis of a variety of bis(catecholato)germanes is reported. The Lewis acidity of the bis(catecholato)germanes was assessed using the experimental Gutmann-Beckett method and computational FIA and GEI methods. The oligomerization of alkenes using bis(catecholato)germanes demonstrates the use of these complexes in catalysis. The use of donor additives in the dimerization of alpha-methylstyrene resulted in selectivity control comparable to transition metal catalyst systems.

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