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Article

New Insights into Xantphos/Pd-Catalyzed C−N Bond Forming Reactions: A Structural and Kinetic Study

Supporting Info

Liane M. Klingensmith, Eric R. Strieter, Timothy E. Barder, and Stephen L. Buchwald*

Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139

Organometallics, 2006, 25 (1), pp 82–91

DOI: 10.1021/om050715g

Publication Date (Web): December 8, 2005

In papers with more than one author, the asterisk indicates the name of the author to whom inquiries about the paper should be addressed.

Abstract

Both (Xantphos)Pd(dba) and Pd(Xantphos)₂ were identified in mixtures of Pd₂(dba)₃ and Xantphos by use of ³¹P NMR and independent syntheses. At high ligand concentrations, Pd(Xantphos)₂ was found to be the predominant species. Reaction calorimetry was employed to determine whether the formation of Pd(Xantphos)₂ affects the rate at which the Pd-catalyzed C−N bond formation occurs between 4-tert-butylbromobenzene and morpholine. Indeed, the concentration of Xantphos dramatically influences the activity of the catalyst, with high concentrations of Xantphos inhibiting the reaction rate due to the formation of Pd(Xantphos)₂. Two plausible hypotheses for the low activity of Pd(Xantphos)₂ as a precatalyst are (1) a slow rate of Xantphos dissociation from Pd(Xantphos)₂ inhibits the formation of an active (Xantphos)Pd⁰ species and (2) the high degree of insolubility of Pd(Xantphos)₂ results in the precipitation of a significant fraction of the precatalyst from the reaction mixture. Although the equilibrium constant for ligand dissociation could not be determined by either magnetization transfer or variable-temperature experiments due to its slow rate, the more soluble Pd(4,7-di-tert-butylXantphos)₂ complex demonstrated different activity relative to Pd(Xantphos)₂. A comprehensive study of these two complexes indicates that the lower activity of the bis-ligated Pd species is a result of a combination of aforementioned processes, i.e., the slow rate of ligand dissociation and the insolubility of Pd(Xantphos)₂, with the rate of ligand dissociation serving as the primary turnover-limiting factor.