Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)
Infobox disclaimer and references
1,2-Bis(diphenylphosphino)ethane (dppe) is a commonly used bidentate ligand in coordination chemistry. Dppe is almost invariably chelated, although there are examples of unidentate (e.g., W(CO)5(dppe)) and of bridging behavior.[1]
Treatment of dppe with conventional oxidants such as hydrogen peroxide (H2O2), aqueous bromine (Br2), etc., always produces dppeO in low yield (e.g., 13%) as a result of non-selective oxidation leading to mixtures of the starting material, the monoxide, and dioxide.[4] Selective mono-oxidation of dppe can be achieved by reaction with PhCH2Br to give dppeO.
Coordination complexes of dppe, and diphosphine ligands in general, are almost entirely used as homogeneous catalysts for a wide range of reactions. Chiral diphosphines are especially important to the pharmaceutical industry[5] for their ability to catalyze asymmetric reactions[6] Two simple coordination complexes of dppe include Pd(dppe)2 and Ir(dppe)2. Pd(dppe)2 can be prepared by reduction of Pd(II) with NaBH4. It is most conveniently prepared, however, in situ from Pd(OAc)2.[4]
References
^ Cotton, F.A.; Wilkinson, G. Advanced Inorganic Chemistry: A Comprehensive Text, 4th ed.; Wiley-Interscience Publications: New York, NY, 1980; p.246. ISBN 0-471-02775-8
^ Girolami, G.; Rauchfuss, T.; Angelici, R. Synthesis and Technique in Inorganic Chemistry, 3rd ed.; University Science Books: Sausalito, CA, 1999; pp. 85-92. ISBN 0-935702-48-2
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