Reductive elimination rates

In direct reductive elimination path (b), more electron-donating L tends to reduce the reductive elimination rate and more electron-withdrawing L enhances the reactivity to the contrary. Although no systematic data have been presented, this trend is now widely accepted and supported by theoretical examinations [8]. 

In contrast to triphenylphosphine-modified rhodium catalysis, a high aldehyde product isomer ratio via cobalt-catalyzed hydroformylation requires high CO partial pressures, eg, 9 MPa (1305 psi) and 110°C. Under such conditions alkyl isomerization is almost completely suppressed, and the 4.4 1 isomer ratio reflects the precursor mixture which contains principally the kinetically favored -butyryl to isobutyryl cobalt tetracarbonyl. At lower CO partial pressures, eg, 0.25 MPa (36.25 psi) and 110°C, the rate of isomerization of the -butyryl cobalt intermediate is competitive with butyryl reductive elimination to aldehyde. The product n/iso ratio of 1.6 1 obtained under these conditions reflects the equihbrium isomer ratio of the precursor butyryl cobalt tetracarbonyls (11). 

Recent tlieotetical studies of reductive elimination ftoni Me- Cu-S in tlie presence of BF suggest tliat reaction rate of tlie conjugate addition can inctease if one of tlie Me groups is detadied ftoni tlie coppetflll) to bind witli a hot on atom rsdienie I0.I2)[I29],... 

The general catalytic cycle for the coupling of aryl-alkenyl halides with alkenes is shown in Fig. 9.6. The first step in this catalytic cycle is the oxidative addition of aryl-alkenyl halides to Pd(0). The activity of the aryl-alkenyl halides still follows the order RI > ROTf > RBr > RC1. The olefin coordinates to the Pd(II) species. The coordinated olefin inserts into Pd—R bond in a syn fashion, p-Hydrogen elimination can occur only after an internal rotation around the former double bond, as it requires at least one /I-hydrogen to be oriented syn perpendicular with respect to the halopalladium residue. The subsequent syn elimination yields an alkene and a hydridopalladium halide. This process is, however, reversible, and therefore, the thermodynamically more stable (E)-alkene is generally obtained. Reductive elimination of HX from the hydridopalladium halide in the presence of a base regenerates the catalytically active Pd(0), which can reenter the catalytic cycle. The oxidative addition has frequently assumed to be the rate-determining step. 

They demonstrated that electron-deficient R groups and electron-rich R substituents at S accelerated the reductive elimination. They proposed 123 (Lj = DPPE, R = Ph, R = Ar) as a transition state, where R acts as an electrophile and thiolate as a nucleophile. The Hammet plot for the reductive elimination showed that the resonance effect of the substituent in R determines the inductive effect of the R group, and the effect in SR showed an acceptable linear relationship with the standard o-values. The relative rate for sulfide elimination as a function of the hybrid valence configuration of the carbon center bonded to palladium followed the trend sp > sp spl... 

Isotope effects indicate that the collapse of the adduct by reductive elimination is the rate-determining step.54 Theoretical treatments of the mechanism suggest similar intermediates. (See Section 8.1.2.7 for further discussion of the computational results.)55... 

The mechanism of carbometallation has been explored computationally.77 The reaction consists of an oxidative addition to the triple bond forming a cyclic Cu(m) intermediate. The rate-determining step is reductive elimination to form a vinyl magnesium (or zinc) reagent, which then undergoes transmetallation to the alkenyl-copper product. 

Reductive elimination, though usually not a rate-limiting step, may seriously affect the reaction outcome, particularly in those cases when side reactions may occur in the intermediate complex, e.g., Pd hydride elimination in the case when alkyl groups are involved, leading to the loss of regioselectivity. 

Cross-coupling to form carbon heteroatom bonds occurs by oxidative addition of an organic halide, generation of an aryl- or vinylpalladium amido, alkoxo, tholato, phosphido, silyl, stannyl, germyl, or boryl complex, and reductive elimination (Scheme 2). The relative rates and thermodynamics of the individual steps and the precise structure of the intermediates depend on the substrate and catalyst. A full discussion of the mechanism for each type of substrate and each catalyst is beyond the scope of this review. However, a series of reviews and primary literature has begun to provide information on the overall catalytic process.18,19,22,23,77,186... 

W.L. Gladfelter, University of Minnesota The thermolysis of arachno-[(CO)H(PMe3)2(IrB8H12)], in which H2 is evolved, is an example of a dinuclear reductive elimination. Have you observed any dependence of the rate on the PMe3 concentration Also, do the compounds undergo H/D exchange when placed in a D2 atmosphere ... 

The cyclodimers are liberated from the respective elimination products 8a and 10a via successive substitution processes with incoming butadiene, that regenerates the active catalyst la in an overall exergonic process. For the rate determining reductive elimination step of the C8-channel free-energy activation barriers of 20.1-24.1 kcalmol-1 are predicted for catalysts TTV, that are in excellent agreement with experimental estimates.43 Thus, moderate reaction conditions are required for the catalytic cyclodimerization of 1,3-butadiene.6... 

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