Complexes diphosphine ligands

Elimination reactions have been particularly studied in the case of dialkyls. They depend on the alkyl groups being cis trans-complexes have to isomerize before they can eliminate, and a complex with a trans-spanning diphosphine ligand is stable to 100°C (Figure 3.56). 

Significant advance in the field of asymmetric catalysis was also achieved with the preparation of l,2-bis(phospholano)benzene (DuPHOS 4) and its confor-mationally flexible derivative (l,2-bis(phospholano)ethane, known as BPE) by Burk et al. [59]. Two main distinctive features embodied by these Hgands, as compared to other known chiral diphosphine ligands, are the electron-rich character of the phosphorus atoms on the one hand and the pseudo-chirality at phosphorus atoms, on the other. These properties are responsible for both the high activity of the corresponding metal complex and an enantioselection indepen-... 

Manufacture of rhodium precatalysts for asymmetric hydrogenation. Established literature methods used to make the Rh-DuPhos complexes consisted of converting (1,5-cyclooctadiene) acetylacetonato Rh(l) into the sparingly soluble bis(l,5-cyclooctadiene) Rh(l) tetrafluoroborate complex which then reacts with the diphosphine ligand to provide the precatalyst complex in solution. Addition of an anti-solvent results in precipitation of the desired product. Although this method worked well with a variety of diphosphines, yields were modest and more importantly the product form was variable. The different physical forms performed equally as well in hydrogenation reactions but had different shelf-life and air stability. 

An especially important case is the enantioselective hydrogenation of a-amidoacrylic acids, which leads to a-aminoacids.29 A particularly detailed study has been carried out on the mechanism of reduction of methyl Z-a-acetamidocinnamate by a rhodium catalyst with a chiral diphosphine ligand DIPAMP.30 It has been concluded that the reactant can bind reversibly to the catalyst to give either of two complexes. Addition of hydrogen at rhodium then leads to a reactive rhodium hydride and eventually to product. Interestingly, the addition of hydrogen occurs most rapidly in the minor isomeric complex, and the enantioselectivity is due to this kinetic preference. 

Oxidative addition of a silyl-protected 4-(bromomethyl)phenol precursor to (tme-da)Pd(II)Me2 (tmeda = tetramethylethylenediamine), followed by ethane reductive elimination, resulted in formation of the benzylic complex 16 (Scheme 3.10). Exchange of tmeda for a diphosphine ligand (which is better suited for stabilizing the ultimate Pd(0) QM complex), followed by removal of the protecting silyl group with fluoride anion, resulted in the expected p-QM Pd(0) complex, 17, via intermediacy of the zwitterionic Pd(II) benzyl complex. In this way a stable complex of p-BHT-QM, 17b, the very important metabolite of the widely used food antioxidant BHT20 (BHT = butylated hydroxytoluene) was prepared. Similarly, a Pd(0) complex of the elusive, simplest /)-QM, 17a, was obtained (Scheme 3.10). 

Other chiral diphosphine ligands (374), (375), (376), and (377) bind to iridium with little diastereoselectivity.603 The complexes are characterized by 1H and 31P H NMR spectroscopy. 

Dinuclear complexes with bridging phosphido, hydrido, and diphosphine ligands were formed via some interesting transformations, such as P—C bond formation, P—H bond activation, and conversion of a chelate diphosphine to one bridging two metal centers.259... 

The studies on palladium-phosphine complexes, especially those with diphosphine ligands, have mainly been focused on the complexes of palladium in lower oxidation state of 0 and 1 84,580,581,583,766,787,788,811-816 suc]1 as [Pd2(dppm)2]2+, [Pd2(dppm)3],815 [Pd3(dppm)3(/i3-... 

The characterization and crystal structure of the dimer [Pt2( -dppm)3] (dppm = bis(diphenyl-phosphino)methane), first reported as a deep red complex in 1978, was described by Manojlovic-Muir et al. in 1986.11 The structure, the first of its type, is made up of two parallel and almost eclipsed trigonal-planar platinum moieties bridged by three diphosphine ligands. The Pf Pt separation is 3.0225(3) A, too long to be considered a bond.11 [Pt2(//-dppm)3] catalyzes the hydrogenation/reduction of carbon dioxide with dimethylamine to give dimethylformamide12 (Equation (1)) and the reverse reaction.13... 

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