Affiliation:
1. Leibniz Institut für Katalyse e.V. Albert-Einstein-Straße 29a 18059 Rostock Germany
2. DSM-Firmenich Wurmisweg 576 4303 Kaiseraugst Switzerland
Abstract
AbstractAn efficient and highly selective semi‐hydrogenation of terminal alkynes to alkenes using neutral dimeric rhodium(I) complexes of the type [Rh(μ‐Cl)(PP)]2 is presented. Dehydroisophytol (DIP) was chosen as the alkyne for this study because of its high importance in the industrial production of synthetic vitamin E. Excellent selectivity of over 91% towards the alkene was achieved with known and new rhodium catalysts. No deactivation was observed for the [Rh(μ‐Cl)(PP)]2 complexes and the molar Rh:DIP ratio could be increased to 1:20 000, and importantly, no reduction in selectivity was observed. The results presented open the door to the industrial application of homogeneous rhodium complexes in the semi‐hydrogenation of terminal alkynes.
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1 articles.
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