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Ligand substitution reactions zinc

Support-bound transition metal complexes have mainly been prepared as insoluble catalysts. Table 4.1 lists representative examples of such polymer-bound complexes. Polystyrene-bound molybdenum carbonyl complexes have been prepared for the study of ligand substitution reactions and oxidative eliminations [51], Moreover, well-defined molybdenum, rhodium, and iridium phosphine complexes have been prepared on copolymers of PEG and silica [52]. Several reviews have covered the preparation and application of support-bound reagents, including transition metal complexes [53-59]. Examples of the preparation and uses of organomercury and organo-zinc compounds are discussed in Section 4.1. [Pg.165]

The pentammine aqua ion [Ru(NH3)j(H20)]2+, best made by zinc amalgam reduction and aquation of [Ru(NH3)5C1]2+, undergoes extensively studied substitution reactions first order in both the ruthenium complex and the incoming ligand (e.g. NH3, py) and is a convenient source of other... [Pg.22]

This reaction was clarified with hexenyl stearate (I) at 60°C during the reaction between zinc stearate and 4-chloro-2-hexene in tetrahydro-furan. During this reaction, zinc stearate reacts immediately with 2 mol of model compound, and kinetic laws do not suggest the presence of CIZnOCOR as an intermediate product in the substitution reaction. Nevertheless, such an organometallic compound was suggested by Frye and Horst (9) and also by Anderson and McKenzie (10) who assumed that such compounds accounted for the ligand exchange between cadmium chloride and barium carboxylate. [Pg.398]


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See also in sourсe #XX -- [ Pg.117 ]




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