[Pd(IPr)(acac)Cl]: An Easily Synthesized, Bulky Precatalyst for C–N Bond Formation

A very straightforward synthesis of [Pd­(IPr*)­(acac)­Cl] has been developed from commercially available Pd­(acac)2 and the easily prepared IPr*·HCl (acac = acetylacetonate; IPr* = N,N′-bis­(2,6-bis­(diphenylmethyl)-4-methylphenyl)­imidazol-2-ylidene). The reactivity of the resulting complex [Pd­(IP...

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Veröffentlicht in:Organometallics 2012-04, Vol.31 (8), p.3402-3409
Hauptverfasser: Meiries, Sebastien, Chartoire, Anthony, Slawin, Alexandra M. Z, Nolan, Steven P
Format: Artikel
Sprache:eng
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Zusammenfassung:A very straightforward synthesis of [Pd­(IPr*)­(acac)­Cl] has been developed from commercially available Pd­(acac)2 and the easily prepared IPr*·HCl (acac = acetylacetonate; IPr* = N,N′-bis­(2,6-bis­(diphenylmethyl)-4-methylphenyl)­imidazol-2-ylidene). The reactivity of the resulting complex [Pd­(IPr*)­(acac)­Cl] (1) as a highly active PdII precatalyst for the Buchwald–Hartwig arylamination coupling has been explored. A wide range of substrates with varying electronic and steric demands of both coupling partners has been screened successfully. The chemoselectivity of the reaction was also explored by using aryl heterodihalides.
ISSN:0276-7333
1520-6041
DOI:10.1021/om300205c