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Palladium atom

II. The change of the sign between these two models may be also important for clustering and the surface growth mechanism. In the selfconsistent theory, the silver atoms tend to establish bonds with palladium atoms, while in the non-selfconsistent theory, the Ag-Ag bonds are favored. This explains the differences between the concentration profiles calculated within the models I and II and the fact that they do not simply follow the variations of the on-site terms. [Pg.137]

From intermediate C, the next step in the catalytic cycle involves a simple bond rotation to give D. This event is essential because it establishes the necessary syn relationship between a -hydrogen and the palladium atom. With a / -hydrogcn and the transition metal... [Pg.567]

The electrophilic character of the palladium atom in the complexes formed by oxidative addition of aryl halides and alkenyl halides to palladium(o) complexes can be exploited in useful ways. [Pg.573]

Such simple considerations led Scholten and Konvalinka to confirm the form of the dependence of the reaction velocity on the pressure, as had been observed in their experiments. Taking into account a more realistic situation, on the polycrystalline hydride surface with which a hydrogen molecule is dealing when colliding and subsequently being dissociatively adsorbed, we should assume rather a different probability of an encounter with a hydride center of a /3-phase lattice, an empty octahedral hole, or a free palladium atom—for every kind of crystallite orientation on the surface, even when it is represented, for the sake of simplicity, by only the three low index planes. [Pg.259]

Fig. 4. The structure of PdO (referred to axes 45° from those of the smallest unit). Large circles represent oxygen, small circles palladium atoms. Fig. 4. The structure of PdO (referred to axes 45° from those of the smallest unit). Large circles represent oxygen, small circles palladium atoms.
Although, as has already been mentioned, under matrix conditions between 10 and 77 K, there is no oxidative addition of a chloroolefin to nickel or palladium atoms (141), it is evident that this is simply a function of reaction and processing conditions, as it has been shown (68) that oxidative addition to C-C or C-H bonds by nickel atoms leads to pseudocomplexes having Ni C H ratios of 2-5 1 2. Klabunde and co-workers investigated the oxidative addition-reactions of palladium atoms with alkyl halides (73) and benzyl chlorides (74). [Pg.158]

As far as the reactions with benzyl chlorides are concerned (74), the oxidative addition of benzyl chloride and substituted benzyl chlorides to palladium atoms yields rj -benzylpalladium chloride dimers. The parent compound, bis(l,2,3-7 -benzyl)di-/i,-chloro-palladium(II), quantitatively adds four molecules of PEts by first forcing the rj -benzyl-iy -benzyl transformation, with subsequent breakage of the Pd-Cl bridges to form trans-bistPEtsKbenzyDchloroPddI). The spectral characteristics of the parent molecule are indicative of the allylic type of bonding. Similar i7 -benzyl compounds were formed from 4-methylbenzyl chloride, 2-chloro-l,l,l-trifluoro-2-phenylethane, and 3,4-dimethylbenzyl chloride. [Pg.160]

Boscoboinik, J.A., Plaisance, C., Neurock, M. and Tysoe, W.T. (2008) Monte Carlo and density functional theory analysis of the distribution of gold and palladium atoms on Au/P(lll) alloys. Physical Review B - Condensed Matter, 77, 045422-1-045422-6. [Pg.243]

Size-selected palladium atoms were deposited on an in. sv /M-prepared MgO(lOO) thin film at 90 K the palladium surface concentration was about 1% of a monolayer. Comparison of ab initio calculations and FTIR studies of CO adsorption provided evidence for single Pd atoms bond to F centres of the MgO support with two CO molecules attached to each palladium atom.24... [Pg.165]

In the case of palladium particles supported on magnesium oxide, Heiz and his colleagues have shown,29 in an elegant study, a correlation between the number of palladium atoms in a cluster and the selectivity for the conversion of acetylene to benzene, butadiene and butane, whereas in the industrially significant area of catalytic hydrodesulfurisation, the Aarhus group,33 with support from theory, have pinpointed by STM metallic edge states as the active sites in the MoS2 catalysts. [Pg.176]

Sherer et al.32 carried out systematic DFT calculations (DFT = density functional calculations) on the compound in question and on pertinent simpler compounds. They optimized the geometric structures and compared the computed bond lengths and bond orders. These authors, too, chose the oxidation state II for the central palladium atom. [Pg.559]

Potentially coordinatively unsaturated dithiolene-metal complexes are rare,298-306 and 1 1 dithiolene-transition-metal complexes with no other ligands are, to our knowledge, unprecedented.307 The neutral complex [PdS2C2(COOMe)2]6,308 is homoleptic containing one dithiolene unit for each palladium atom and no other ligands. Electrochemical reduction of the compound depicted in Figue 21 proceeds in four reversible steps. [Pg.579]

Figure 21 The neutral complex containing one dithiolene unit for each palladium atom and no other... Figure 21 The neutral complex containing one dithiolene unit for each palladium atom and no other...
A trinuclear system, whose structure was published,555 was formed in high yield by the cyclometalation of a l,3-bis(alkylbenzimidazol-2-yl)benzene ligand, followed by the trimerization of the unit, which possesses a vacant coordination site on the palladium atom and a pendant noncoordinated benzimidazole moiety. The resulting product forms a cup-shaped trimer or tricorn, presented in Figure 46, that includes a molecule of acetonitrile in the crystal structure.556... [Pg.602]

The compound [Pd[/i2-(C6H4)PPh2]Brj 4 has [(C6II4)PPh2] anions bridging two palladium atoms in a tetranuclear structure. This tetranuclear frame was cleaved with phosphines to form mononuclear compounds.568 Intermediate products of the frame degradation were detected (see Figure 50).567... [Pg.605]

Figure 86 Compound containing a full M2L4 helical cage that has each square-planar palladium atom coordinated to the four bridging ligands and within which resides a well-ordered PF6 ion. Figure 86 Compound containing a full M2L4 helical cage that has each square-planar palladium atom coordinated to the four bridging ligands and within which resides a well-ordered PF6 ion.
In the second cluster, the two Ru6 octahedra are linked through two palladium atoms. The third cluster contains two additional palladium atoms. The Pd4 skeleton adopts the form of a bent square. The two Ru6 octahedra have local structures similar to those in the second cluster, but their relative orientation is now twisted. Apparently, formation of these heterometallic cluster complexes does not result from a simple combination reaction between cationic and anionic complexes but is accompanied by partial redox reactions.900... [Pg.651]

Conjugated boron polymers containing platimnn or palladium atom in the main chain were also prepared by hydroboration polymerization between tetrayne/ metal complex monomers and tripylborane (scheme 16).30 From gel permeation chromatographic analysis [THF, polystyrene (PSt) standards], the number-average molecular weights of the polymers obtained were found to be 9000. The polymers were soluble in common organic solvents such as THF, chloroform, and benzene. The absorption peaks due to tt-tt transition were observed around 390 nm in the UV-vis spectra of these polymers. The fluorescence emission spectra exhibited intense peaks at 490 nm in chloroform. [Pg.149]


See other pages where Palladium atom is mentioned: [Pg.108]    [Pg.258]    [Pg.259]    [Pg.181]    [Pg.153]    [Pg.158]    [Pg.100]    [Pg.311]    [Pg.21]    [Pg.67]    [Pg.16]    [Pg.235]    [Pg.329]    [Pg.556]    [Pg.558]    [Pg.558]    [Pg.561]    [Pg.596]    [Pg.596]    [Pg.612]    [Pg.630]    [Pg.632]    [Pg.647]    [Pg.653]    [Pg.656]    [Pg.501]    [Pg.502]    [Pg.2]    [Pg.5]    [Pg.5]    [Pg.236]    [Pg.299]    [Pg.304]   
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See also in sourсe #XX -- [ Pg.3 , Pg.10 , Pg.10 , Pg.14 ]

See also in sourсe #XX -- [ Pg.3 , Pg.10 , Pg.10 ]

See also in sourсe #XX -- [ Pg.42 ]




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