Selective Catalysts for the Homogeneous Semi‐Hydrogenation

Author:

Jannsen Nora1ORCID,Pribbenow Cornelia1,Selle Carmen1,Drexler Hans‐Joachim1,Müller Marc‐André2ORCID,Medlock Jonathan A.2ORCID,Bonrath Werner2,Heller Detlef1

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.

Publisher

Wiley

Subject

General Chemistry

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