Iridium Pincer-Catalyzed Dehydrogenation of Ethers Featuring Ethylene as the Hydrogen Acceptor

We describe efficient methods to dehydrogenate ethers by using iridium pincer complexes ( iPr4Anthraphos)-Ir­(H)­(Cl), 4, iPr4PC­(sp3)­P–Ir­(H)­(Cl), 5, and ( iPr4PCP)-Ir­(H)­(Cl), 6. At 120 °C, cyclic ethers were dehydrogenated with tert-butylethylene as the hydrogen acceptor with high turnover num...

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Veröffentlicht in:Organometallics 2015-08, Vol.34 (16), p.4058-4062
Hauptverfasser: Lyons, Thomas W, Bézier, David, Brookhart, Maurice
Format: Artikel
Sprache:eng
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Zusammenfassung:We describe efficient methods to dehydrogenate ethers by using iridium pincer complexes ( iPr4Anthraphos)-Ir­(H)­(Cl), 4, iPr4PC­(sp3)­P–Ir­(H)­(Cl), 5, and ( iPr4PCP)-Ir­(H)­(Cl), 6. At 120 °C, cyclic ethers were dehydrogenated with tert-butylethylene as the hydrogen acceptor with high turnover numbers (over 400 in many cases). Acyclic ethers such as diethyl ether can also be dehydrogenated catalytically with TONs up to 90. The efficient dehydrogenation of cyclic and acyclic ethers using ethylene as a more practical hydrogen acceptor has been demonstrated for the first time.
ISSN:0276-7333
1520-6041
DOI:10.1021/acs.organomet.5b00501