Autor: |
Verhoeven DGA; Organic Chemistry & Catalysis Debye Institute for Nanomaterials Science Faculty of Science Utrecht University Universiteitsweg 99 3584 CG Utrecht The Netherlands., Kwakernaak J; Organic Chemistry & Catalysis Debye Institute for Nanomaterials Science Faculty of Science Utrecht University Universiteitsweg 99 3584 CG Utrecht The Netherlands., van Wiggen MAC; Organic Chemistry & Catalysis Debye Institute for Nanomaterials Science Faculty of Science Utrecht University Universiteitsweg 99 3584 CG Utrecht The Netherlands., Lutz M; Crystal and Structural Chemistry Bijvoet Center for Biomolecular Research Utrecht University Padualaan 8 3584 CH Utrecht The Netherlands., Moret ME; Organic Chemistry & Catalysis Debye Institute for Nanomaterials Science Faculty of Science Utrecht University Universiteitsweg 99 3584 CG Utrecht The Netherlands. |
Jazyk: |
angličtina |
Zdroj: |
European journal of inorganic chemistry [Eur J Inorg Chem] 2019 Feb 07; Vol. 2019 (5), pp. 660-667. Date of Electronic Publication: 2019 Jan 28. |
DOI: |
10.1002/ejic.201801221 |
Abstrakt: |
The hydrosilylation of unsaturated compounds homogeneously catalyzed by cobalt complexes has gained considerable attention in the last years, aiming at substituting precious metal-based catalysts. In this study, the catalytic activity of well-characterized Co II and Co I complexes of the p Tol dpbp ligand is demonstrated in the hydrosilylation of 1-octene with phenylsilane. The Co I complex is the better precatalyst for the mentioned reaction under mild conditions, at 1 mol-% catalyst, 1 h, room temperature, and without solvent, yielding 84 % of octylphenylsilane. Investigation of the substrate scope shows lower performance of the catalyst in styrene hydrosilylation, but excellent results with allylbenzene (84 %) and acetophenone (> 99 %). This catalytic study contributes to the field of cobalt-catalyzed hydrosilylation reactions and shows the first example of catalysis employing the dpbp ligand in combination with a base metal. |
Databáze: |
MEDLINE |
Externí odkaz: |
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