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Dihydrogen complexes heterolytic cleavage

The reaction of OsHCl(CO)(P Pr3)2 with HC1 gives the dichloro derivative OsCl2( n2-H2)(CO)(PIPr3)2.35 In solution, this complex is stable under argon for a matter of days. However, the dihydrogen unit is highly activated toward heterolytic cleavage, as demonstrated by deprotonation with NaH and by reactions with carbon monoxide and /ert-butyl isocyanide, which afford OsHCl(CO)L(P Pr3)2 (L = CO, r-BuNC) and HC1. [Pg.21]

One of the important properties of dihydrogen ligands, particularly in charged transition metal complexes, is their ability to nndergo heterolytic cleavage [9]. In addition, protonation of transition metal hydrides with acids is a common method for preparation of transition metal dihydrogen complexes ... [Pg.33]

Scheme 10.2 Heterolytic cleavage of dihydrogen on platinum SPO complex. Scheme 10.2 Heterolytic cleavage of dihydrogen on platinum SPO complex.
The hypothetical reaction mechanism shown in Fig. 10 is a variation of Scheme (3), and is consistent with the redox and pH dependence of the EPR-detectable nickel species (65). Hydrogen is known to undergo heterolytic cleavage (81) it is proposed that this is an intramolecular reaction, leading to the formation of a nickel (II) hydride and a protonated base in the enzyme (Step 1 in Fig. 10). The Ni-C species is postulated to be a protonated Ni(I) species. An alternative formulation for this state would be a dihydrogen complex, Ni(III) H2, as suggested by Crabtree (104). Ultimately the exact mechanism can only be determined by kinetic measurements. [Pg.321]

Jia and Morris reported that (dihydrogen)ruthenium(II) complex formulated as [RuCp(H2)L2] produces a proton by heterolytic cleavage of the coordinated H-H bond [77]. Of particular interest is that the pK values of these complexes closely depend on the ancillary ligand employed (pK = 4.9-9.0 in THE), suggesting that a decrease in the electron density of the metal increases the acidity of the dihydrogen complex. [Pg.362]

Scheme 1. Steps in the heterolytic cleavage of dihydrogen on Ru(II) starting with the complex trans-Ru(0S02CF3)(CN)(dppe)2. Scheme 1. Steps in the heterolytic cleavage of dihydrogen on Ru(II) starting with the complex trans-Ru(0S02CF3)(CN)(dppe)2.
Heterolytic Cleavage of Dihydrogen by Ruthenium and Molybdenum Complexes... [Pg.117]

Some hydride complexes (Equation 3.100) are produced by the heterolytic cleavage of Hj, a reaction that probably proceeds through the deprotonation of an intermediate dihydrogen complex. Other hydride complexes (Equation 3.101) are produced by the hydrogenolysis of metal-alkyl bonds. ... [Pg.125]


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See also in sourсe #XX -- [ Pg.106 , Pg.107 ]




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Complex dihydrogen

Dihydrogen heterolytic cleavage

Heterolytic

Heterolytic cleavage

Heterolytic complexes

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