Finding
Thus, a 1:1 adduct 7 was formed by the coordination of one THF molecule to the Pd center and removal of the Pd–arene interaction.
Paper
Palladium-oxygen and palladium-arene interactions in complexes derived from biaryl aminocarbenes: comparison with biaryl phosphanes.
Abstract
The spectacular progress in homogeneous catalysis can be attributed largely to the development of a diverse range of ligand frameworks. The fine-tuning of steric and electronic factors has led to extremely active and selective catalysts. A good example is the recent advances that have been made in Pd-catalyzed cross-coupling reactions with biaryl phosphanes (Scheme 1).[1] Efforts to rationalize the unique behavior of these ligands have led to the substantiation both experimentally and computationally of the critical role of weak Pd–arene and Pd-X (X = O or N) interactions.[2–6] Scheme 1 Structures of the biaryl phosphanes A and B, and of the related biaryl aminocarbenes 1 and 2. The development of N-heterocyclic carbenes as ligands also represents a major breakthrough in homogeneous catalysis.[7] Our interest in increasing further the structural variety of available stable carbenes[8] prompted us to investigate the possibility of preparing monoaminocarbenes (MACs)[9] that feature the same topology as that of biaryl phosphanes.[10–12] Herein we report the synthesis and characterization of the MACs 1 and 2, which are related to A (SPhos: R = cyclohexyl) and MeO-MOP (B),[13] respectively. We show that the coordination of these carbenes to the Pd(allyl)+ fragment is accompanied by secondary interactions, albeit of a markedly different nature to those encountered with the corresponding biaryl phosphanes. A rare Pd–oxygen contact was authenticated structurally by using the stable biphenylcarbene 1, and spectroscopic evidence for an unprecedented, reversible Pd–arene interaction was obtained when the persistent binaphthylcarbene 2 was used as a ligand. The carbene 1 was obtained readily by treatment of the corresponding iminium triflate[14] with 2,2,6,6-tetramethylpiperidinolithium (TMPLi) in THF at −80°C (Scheme 2). The MAC 1 is stable indefinitely in solution at room temperature and was characterized unambiguously on the basis of a 13C NMR signal at δ = 305 ppm.[11a,b] The in situ coordination of 1 upon treatment with [{Pd(allyl)(μ-Cl)}2] afforded the corresponding air-stable complex 3 in 63% yield.[14] In the solid state, [15] the MAC complex 3 exhibits typical Pd–C (2.03 A) and C–N (1.31 A) bond distances,[12,16] but no secondary interaction. To favor the participation of the biphenyl skeleton in the coordination, complex 3 was treated with AgBF4 in CH2Cl2. The pronounced desymmetrization of the two methoxy groups (δH = 4.12/3.68 ppm, δC = 71.6/56.1 ppm) upon cationization strongly supports the formation of a Pd–O contact. This hypothesis was confirmed by an X-ray diffraction study (Figure 1). The short Pd–O distance (2.21 A)[17] indicated unambiguously the presence of a bonding interaction. This Pd–O contact contrasts markedly with the Pd–arene interactions commonly encountered in the related SPhos and MeO-MOP complexes, [3c,4a,d,f] a difference that may be attributed to the different orientations of the Ccarbene–Pd and P–Pd bonds with respect to the biphenyl skeleton (Pd–Cccarbene-Cipso-Cortho: 78° in 3, 86° in 4 versus Pd-P-Cipso-Cortho: 0–10°). Surprisingly, evidence for such Pd–O contacts has been observed only once for biaryl phosphanes, by NMR spectroscopy.[4e] Figure 1 Molecular views (thermal ellipsoids at 50% probability) of complexes 4 (left) and 7 (right) in the solid state. Hydrogen atoms are omitted for clarity. Scheme 2 Neutral and cationic allyl palladium(II) complexes derived from the biphenyl MAC 1. Tf = trifluoromethanesulfonyl. We then turned our attention to the binaphthylaminocarbene 2, which is related to MeO-MOP (B). The corresponding iminium salt was deprotonated with KHMDS at −80 °C in THF (Scheme 3).[14] Carbene 2 is only moderately stable at room temperature (t½ ≈ 30 min) and was therefore characterized at − 78 °C. Its structure was confirmed unambiguously on the basis of the diagnostic 13C NMR signal observed at δ = 307 ppm. In situ coordination of 2 to {Pd(allyl)Cl} occurred at low temperature to give the air-stable complex 5 in 47% yield.[14] X-ray diffraction analysis indicated the absence of a secondary interaction. Scheme 3 Neutral and cationic allyl palladium(II) complexes derived from the binaphthyl MAC 2. HMDS = hexamethyldisilazane. We anticipated that the anti orientation of the methoxy substituent with respect to the palladium center would preclude a Pd–O interaction in the corresponding cationic complex. To determine whether the binaphthyl skeleton may engage in Pd–arene interactions, the cationic complex 6 was prepared by chloride abstraction with AgBF4 in CH2Cl2. The signals for the methoxy groups remained virtually unchanged in the NMR spectra (ΔδH = 0.16 ppm, Δδc = 1.9 ppm), in agreement with the absence of a Pd–O contact in 6. Careful inspection of the 13C NMR spectrum revealed that two of the signals for the carbon atoms of the binaphthyl skeleton are shifted upfield to a significant extent in this cationic complex (δ = 99.3 and 112.0 ppm in 6 versus δ > 122 ppm in 5). This situation is reminiscent of that observed for some binaphthylphosphane complexes[4d–f] and strongly suggests weak η2 coordination of the naphthyl backbone to the Pd center. The two diagnostic high-field signals observed for 6 were assigned unambiguously to C9′ and C10′ on the basis of 2D NMR experiments (see Scheme 3 for atom numbering). This interaction contrasts with the η2 bonding through C1′/C2′ encountered in the related MeO-MOP complexes. In fact, Pd–arene interactions involving the remote ring of the binaphthyl skeleton, as observed in 6, are unknown in biaryl phosphanes. In the case of 6, the interaction most likely results from the configuration of the binaphthyl axis. Crystals of 6 suitable for X-ray diffraction analysis could only be obtained upon cooling a solution of 6 in THF to −30 °C. The modest quality of the crystallographic data precludes discussion of the geometric parameters, but the connectivity of the complex was established unambiguously (Figure 1). Thus, a 1:1 adduct 7 was formed by the coordination of one THF molecule to the Pd center and removal of the Pd–arene interaction. The dissolution of 7 in CDCl3 returned 6 along with free THF in a further illustration of the hemilabile character of the aminobinaphthylcarbene 2. Thus, as observed for the related biaryl phosphanes SPhos and MeO-MOP, the coordination of the biaryl aminocarbenes 1 and 2 to the {Pd(allyl)}+ fragment is accompanied by secondary interactions. The formal replacement of the phosphane group with an aminocarbene moiety influences markedly the relative positions of the metal fragment and the biaryl skeleton, so that unusual Pd–O and Pd–arene interactions are found with the hybrid ligands 1 and 2. Biaryl aminocarbenes further expand the structural diversity of bidentate ligands based on aminocarbenes.[18] Their hemilabile character,[19] which has been substantiated spectroscopically by reversible competition between η2 naphthyl coordination and coordination by THF, may offer interesting perspectives in catalysis. Complex 3 derived from the biphenylaminocarbene 1 was evaluated as a catalyst for the α arylation of propiophenone.[20,21] With a precatalyst loading of 2 mol%, bromobenzene underwent quantitative coupling with propiophenone at room temperature within 15 h. Although the reaction proceeded more slowly, chlorobenzene also acted as an effective arylating agent under the same conditions.[14] According to these preliminary results, the MAC complex 3 competes with the most active phosphane-based catalysts reported to date for the coupling of aryl bromides. Indeed, binap (2,2′-bis(diphenylphosphanyl)-1,1′-binaphthyl) ligands,[20] bis(diarylphosphanyl)ferrocene derivatives,[21] and biphenylphosphanes[22a,b] are typically used at temperatures higher than 50 °C, and only PtBu3,[21b] DtBPF (1,1′-bis(di-tert-butylphosphanyl)ferrocene),[21b] and binaphthyl(dialkyl)phosphanes[22c] were found to be suitable for the coupling of aryl bromides at room temperature. The reaction of chlorobenzene at room temperature is also encouraging, as, until now, aryl chlorides have only been coupled at high temperatures,[20,21b,22a,b,23] except with cyclic alkyl aminocarbenes.[24] Given the superiority of cyclic carbenes over their acyclic counterparts as robust ligands for transition metals,[25] better catalytic results can be expected with cyclic biaryl aminocarbenes, the preparation of which is under active investigation.
Authors
Joan Vignolle, H. Gornitzka, B. Donnadieu
Journal
Angewandte Chemie