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Ligand Cu complexes

TABLE 7.4 Influence of ct-Amino Acid Ligands on the Equilibrium Constant for Binding of 3.8c to the Ligand-Cu Complex (K ) and the Second-Order rate Constant (fccat) for Reaction of this Ternary Complex with Diene 2 and the Enantioselectivity of this Reaction in Water ... [Pg.166]

On the other hand, an attempt to accelerate the step of coordination of the substrate to the Cu catalyst was successful because it used the hydrophobic domain of the polymer ligand156 That was the oxidation catalyzed by polymer-Cu complexes in a dilute aqueous solution of phenol, which occurred slowly. The substrate was concentrated in the domain of the polymer catalyst and was effectively catalyzed by Cu in the domain. A relationship was found to exist between the equilibrium constant (Ka) for the adsorption of phenol on the polymer ligand and the catalytic activity (V) of the polymer-ligand-Cu complex for various polymer ligands K a = 0.21 1/mol and V = 1(T6 mol/1 min for QPVP, K a = 26 and V = 1(T4 for PVP, K a = 52 and V = 10-4 for the copolymer of styrene and 4-vinylpyridine (PSP) (styrene content 20%), and K a = 109 and V = 10-3 for PSP (styrene content 40%). The V value was proportional to the Ka value, and both Ka and V increased with the hydrophobicity of the polymer ligand. The oxidation rate catalyzed by the polymer-Cu complex in aqueous solutions depended on the adsorption capacity of the polymer domain. [Pg.75]

Few other asymmetrie reactions have been performed using insoluble or soluble polymer-supported ligands. The first example is a Mukaiyama-aldol condensation between silyl ketene acetal and different aldehydes using polymeric Box analog of 99 as chiral ligands and Cu(OTf)2 as metal soiu ce in water (Scheme 147) [216]. When using benzaldehyde as substrate, yields were very low (12-34%) and ee were moderate (40-62%) whatever the polymer-supported Box. The same level of enantioseleetivity was observed with other aldehydes while the yield was better with all the ligand/Cu complexes used. [Pg.160]

CU4S4] species in which the TADDOL-derived ligand was an unexpected sul-fur-monodentate and not a S/X-bidentate ligand. This hypothesis was confirmed by NOE NMR spectroscopy that suggested a different structure for the Cu complex of the alcohol ligand relative to the methylether and the dimethylamino ligands, which could explain the observed stereochemical inversion. [Pg.82]

The first copper(I) complex of tris(hydroxymethyl)phosphine ((760) tetrahedral) has been reported by Samuelson and co-workers. This group addressed the question of anion-controlled nuclearity and metal-metal distances in copper(I)-bis(diphenylphosphino)methane complexes, and in this endeavor they reported the structures of complexes (761) (Cu-Cu separation 3.005-3.128 A), (762) (Cu-Cu separation 3.165 A) and (763) (tetrahedral Cu-Cu 3.293 A). 6 They synthesized and provided structural evidence of oxy anion- encapsulated copper(I) complexes of this ligand. The complexes (764) (distorted tetrahedral Cu-Cu 3.143 A), (765) (distorted tetrahedral Cu-Cu 3.424A), (766) (distorted trigonal Cu-Cu 3.170A), and (767) (Cu-Cu 3.032-3.077A) were reported. They studied solid-state emission spectra of these complexes.567 During this pursuit they... [Pg.890]

Recently, Scott et al. have reported that a Cu complex bearing an axially chiral ligand (49) is an excellent catalyst for aziridination of 2,2-dimethylchromene and cinnamate esters (Scheme 36), though it is also less efficient for the reactions of simple olefins.157,158 On the basis of DFT investigation of the nitrenoid intermediate (50), one of the oxygen atoms of the A -sulfonyl group has been proposed to be interacting with the nitrene N-atom.158... [Pg.229]

Dichalcogenolene ligands form complexes with main group and d transition metal ions.103 Bis( 1,2-dithiolene) complexes have been obtained for metals, such as Cr, Mn, Ni, Cu, Zn, for the first row, Pd, Ag, and Cd for the second row, and Pt, Au, and Hg for the third row. Homoleptic /ra(l,2-dithiolcnc) complexes have been obtained for Ti, V, Cr, Zr, Nb, Mo, Tc, Ru, Ta, W, Re, and Os. Fe and Co have been found both in bis and /ra(l,2-dithiolene) complexes, although /ra(l,2-dithiolene) complexes containing these metal ions... [Pg.806]

From the examples shown in Fig. 4.43, we may conclude that the 18e triply hyperbonded complexes are often the stable end-products of successive ligand cu-additions to normal-valent parent species, which is consistent with the well-known 18-electron rule. However, incompletely hyperbonded complexes of 12e, 14e, or 16e count are certainly stable as isolated equilibrium species, and in favorable cases the sequence of cu-additions may also achieve equilibrium configurations exceeding the 18e count, as the example of [PtF8]2 has demonstrated.44... [Pg.477]

Scheme 17. Selectivities exhibited by various ligand-Cu(OTf)2 complexes in the crotonylimide Diels—Alder reaction of cyclopentadiene. [Adapted from (211, 212).]... Scheme 17. Selectivities exhibited by various ligand-Cu(OTf)2 complexes in the crotonylimide Diels—Alder reaction of cyclopentadiene. [Adapted from (211, 212).]...
Mixed-ligand Cu(II) complexes with salicylato and phenanthroline derivatives as ligands can also be highly cytotoxic (231). Mixed-ligand Cu(II) amino acid phenanthroline complexes (Casiopeinas) such as [Cu(L-Ser)(phen)(H20)]+ 52 are reported to be effective anticancer agents (232). It is possible that a complex in this class will soon enter clinical trials. [Pg.221]

When a cupric salt is added to a polymer-ligand solution, a greenSpectroscopic study indicated that complex formation between Cu and a polymer-ligand was not a step-by-step mechanism and that the composition of the complex, Cu(ligandK, in a polymer ligand remained constant throughout the course of the reaction ( ). [Pg.149]

In order to study the shape of a polymer-Cu complex, viscometric measurements of a homogeneous solution of QPVP were carried out (Fig. 1). At constant QPVP concentration, an increase in the added amount of Cu ions causes a decrease in viscosity, which reveals that the polymer-ligand chain is markedly contracted due to intra-polymer chelation. An intra-polymer chelate takes a very compact form and Cu ions are crowded within the contracted polymer chain (Scheme 2). The adsorption of Cu ions on the polymer ligand is sigmoidal, as can be seen in Fig. 1. At a low... [Pg.149]


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See also in sourсe #XX -- [ Pg.181 , Pg.359 ]




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