Affiliation:
1. Institut für Chemie Universität Rostock Albert-Einstein-Straße 3a 18059 Rostock Germany
2. Leibniz-Institut für Katalyse e.V. an der Universität Rostock Albert-Einstein-Straße 29a 18059 Rostock Germany
Abstract
AbstractThe chlorination of 1,2‐diphosphinobenzene with PCl5 to 1,2‐bis(dichlorophosphino)benzene was performed with high yields (93 %) despite the high number of P−H functions. The method was further applied to other phosphanes, enabling the first synthesis and complete characterization of 1,2,4‐tris(dichlorophosphino)benzene (89 % yield) and 1,2,4,5‐tetrakis(dichlorophosphino)benzene (91 % yield), valuable precursors for example for binuclear complexes, coordination polymers, organic wires, or metal–organic frameworks. The application of the chlorophosphanes in base induced ring closure reactions with primary amines is demonstrated.
Funder
Deutsche Forschungsgemeinschaft
Fonds der Chemischen Industrie
Cited by
2 articles.
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