Catalyst supports polystyrene

The other main support used for solid base catalysts is polystyrene, which while it does not have a well-defined porous structure, does swell in solvents providing an accessible high surface area on which to carry out reactions. One common method of chemically attaching groups to polystyrene involves incorporation of specific amounts of styrene contain-... 

An alternative that has received a great deal of attention in recent years is the immobilisation of a chiral catalyst on a nonsoluble support (polystyrene resins, silica gel, zeolites, etc.), thereby creating a chiral heterogeneous catalyst. Unlike homogeneous catalysts, these supported complexes can be recovered from the... 

The latter mechanism is supported by evidence obtained from the initiation and termination steps in the syndiospecific polymerization of styrene [190]. The 13C-enriched titanium catalyst afforded polystyrene with a CH(Ph)CH213CH3 end group, which indicates that the initiation step proceeded by secondary insertion (2,1-insertion) of styrene into the Ti-13C bond of the active species (Eq. 10). In contrast to this mechanism, termination by the addition of 13C-enriched methanol or tert-butyl alcohol afforded polymers without 13CH30 or tertbutoxy end groups. 

Show by equations how to synthesize each of the following polymer catalysts a. Polystyrene support with — P2PtCl2 catalyst group... 

Variation in % CL of the catalyst support most likely affects intraparticle diffusion more than it affects intrinsic reactivity. Increased cross-linking causes decreased swelling of the polymer by good solvents. Thus the overall contents of the gel become more polystyrene-like and less solvent-like as the % CL is increased. Fig. 5 shows the... 

The first investigations on iron-catalyzed Michael reactions utilized Fe(acac)3 as catalyst. However, this metal complex is itself catalytically almost inactive. Yields of only up to 63% could be achieved, if BF3OEt2 is used as a co-catalyst [55], Polystyrene-bound Fe(acac)3 catalysts were also reported to give yields up to 63% [56], FeCl3 was used as a co-catalyst for clay-supported Ni(II). Yields achieved with this heterogeneous system ranged from 40 to 98% [57]. The double Michael addition of acrylonitrile to ethyl cyanoacetate is smoothly catalyzed by a complex generated from [Fe(N2) (depe)2] [depe = l,2-bis(diethylphosphano)ethane]. At 23 °C and after 36h, an 88% yield is obtained with 1 mol% of this Fe(0) catalyst [58]. 

Heterogeneous chiral catalysts are useful because of the easier separation of catalyst from the product and recovery process than homogeneous chiral catalysts. Heterogeneous chiral catalysts supported on polystyrene-type resin catalyse the highly enantioselective addition of dialkylzincs to aldehydes.17... 

The immobilization of phase transfer catalysts on solid substrates allows a clean reaction with no contamination of the products by the catalyst. Insoluble polystyrene matrices have been used as a solid support. The polymer matrix does not affect the velocity of the reaction, apart from steric hindrance with respect to the reagents. In the case of immobilization on modified silica the active centre is linked to the support by an alkyl chain of variable length. This length strictly determines the adsorption capacity of the polar support, which then controls the rate of reaction. A three-phase catalytic system is set up. Two distinct phases, containing reagents, come into close... 

Fig. 11 Alternative dendritic macromolecular structures based on dendronized polystyrene (left) and hyperbranched polyglycidol (right) used as catalyst supports...

In reactions with polymer-bound catalysts, a mass-transfer limitation often results in slowing down the rate of the reaction. To avoid this disadvantage, homogenous organic-soluble polymers have been utilized as catalyst supports. Oxazaborolidine 5, supported on linear polystyrene, was used as a soluble immobilized catalyst for the hydroboration of aromatic ketones in THF to afford chiral alcohols with an ee of up to 99% [40]. The catalyst was separated from the products with a nanofiltration membrane and then was used repeatedly. The total turnover number of the catalyst reached as high as 560. An intramolecularly cross-linked polymer molecule (microgel) was also applicable as a soluble support [41]. 

Crosslinked polystyrene is a valuable catalyst support, since it is easily functionalized and available with a wide range of physical properties. 

Here, we give an example where the electrochemical and electrocatalytic properties of nanostructured Pt catalysts supported on glassy carbon, prepared with colloidal lithography, were tested with oxidation of preadsorbed CO, so-called CO-stripping, as a test reaction [99]. The Pt nanoparticles were prepared as described in Fig. 4.11, except that the polystyrene particles were removed by UV-ozone treatment. The particles had an average diameter of 122 11 nm and were about 40 nm high. There was no indication (by AFM... 

CH2CI2 solution and was reused for several reductions of B. After three reuses, the catalyst maintained its activity, but the enantiopurity of the products decreased by --10%. The complex did not catalyze the reductions of A, C, or 2 methylquinoxaline, and it was inactive in aqueous solution. On the other hand, the catalysts supported on cross linked polystyrenes with hydrophilic SOjNa or amphiphilic... 

Surface area and pore size distribution studies have been carried out on macroporous polystyrene resins. These showed the catalyst-supported resins had pore sizes in the range 3-30 nm and that the surface area of the system was reduced only slightly during catalyst preparation. ... 

Table 8. Table of Polymer Catalysts using Polystyrene as Support... 

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