“…The phosphine functionality can be introduced to polystyrenes by alternative approaches, such as lithiation (e.g., with butyllithium) followed by a reaction with ClP(C 6 H 5 ) 2 . For example, six different supported Rh-phosphine complexes were identified using NMR spectroscopy in the reaction of phosphinated polystyrene with an Rh-precursor [94]. It was found that the distribution of relatively bulky phosphine groups in the resin was strongly affected by the degree of cross-linking.…”
Section: Functionalized Polymers As Supportsmentioning
“…The phosphine functionality can be introduced to polystyrenes by alternative approaches, such as lithiation (e.g., with butyllithium) followed by a reaction with ClP(C 6 H 5 ) 2 . For example, six different supported Rh-phosphine complexes were identified using NMR spectroscopy in the reaction of phosphinated polystyrene with an Rh-precursor [94]. It was found that the distribution of relatively bulky phosphine groups in the resin was strongly affected by the degree of cross-linking.…”
Section: Functionalized Polymers As Supportsmentioning
“…33). The possible and predictable formation of different organometallic species during the supportation on inorganic matrix has been clearly evidenced in the case of alumina/Cp*TiC13 (Cp* = pentamethylcyclopentadienyl) or alumina/CpTiClj systems (Ref.…”
Macromolecular ligands have been widely used in the past two decades with the objective of preparing structurally defined heterogeneous catalysts from soluble organometallic complexes. This activity has been largely reconsidered and focused on few specific systems. In this connection the present paper reviews recent data concerning the preparation of macromolecular metal complexes derived from transition metals which can produce active catalytic complexes for olefin polymerization and oligomerization and comparison is made about the suitability of both organic resins (crosslinked polystyrene) and inorganic materials (silica, alumina and zeolites).
“…Examples of phosphinated monomers include vinyldiphenylphosphine, allyldiphenylphosphine, and p-diphenylphosphinostyrene; these are copolymerized with styrene (and sometimes divinylbenzene). (28)(29)(30)(31)(32)(33)(34) By varying the amounts of monomers a wide range of ligand loadings and cross-linking densities are possible.…”
Section: Polymerization Of Phosphine Monomersmentioning
confidence: 99%
“…There are just two major contributions in this area. (34,46) Both examined polymers prepared through the polymerization of phosphine monomers; this avoided the complicating effect of an uneven distribution of phosphine sites. These studies examined both cross-linked and noncross-linked polymers.…”
Section: Physiochemical Characteriza Tlon Of Ca Tal Ystsmentioning
confidence: 99%
“…(34) Even with a phosphine function in each repeating unit, up to 200,000 pulses were required. The initial spectrum was different from the final one, apparently reflecting a 0.5-1 hr requirement for ligand exchange to reach equilibrium.…”
Section: Physiochemical Characteriza Tlon Of Ca Tal Ystsmentioning
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