Resins, cross-linked polystyrene

Kaiser oxime resin cross-linked polystyrene with 4-nitrobenzophenone oxime linker Lawesson s reagent 2,4-bis(4-methoxyphenyl)-l, 3-dithia-2,4-diphosphetane-2,4-disulfide... 

Two classes of micron-sized stationary phases have been encountered in this section silica particles and cross-linked polymer resin beads. Both materials are porous, with pore sizes ranging from approximately 50 to 4000 A for silica particles and from 50 to 1,000,000 A for divinylbenzene cross-linked polystyrene resins. In size-exclusion chromatography, also called molecular-exclusion or gel-permeation chromatography, separation is based on the solute s ability to enter into the pores of the column packing. Smaller solutes spend proportionally more time within the pores and, consequently, take longer to elute from the column. 

Divinylbenzene. This is a specialty monomer used primarily to make cross-linked polystyrene resins. Pure divinylbenzene (DVB) monomer is highly reactive polymericaHy and is impractical to produce and store. Commercial DVB monomer (76—79) is generally manufactured and suppHed as mixtures of m- and -divinylbenzenes and ethylvinylbenzenes. DVB products are designated by commercial grades in accordance with the divinylbenzene content. Physical properties of DVB-22 and DVB-55 are shown in Table 10. Typical analyses of DVB-22 and DVB-55 are shown in Table 11. Divinylbenzene [1321 -74-0] is readily polymerized to give britde insoluble polymers even at ambient temperatures. The product is heavily inhibited with TBC and sulfur to minimize polymerization and oxidation. 

A typical system is a chlorome thy late d polystyrene resin cross-linked with 2 or 4% p-divinylbenzene and different amounts of chloromethylated sites (0.7—3.7 mequiv. of Cl per g of polymer) . The reaction is shown schematically in Eq. (6.19) and additional information may be found in Sects. 8.3 and 8.8. 

Strongly basic anion exchange resins, e.g. a cross-linked polystyrene containing quaternary ammonium groups, are largely ionised in both the hydroxide and the salt forms. Some of their typical reactions may be represented as ... 

Organic traps contain isoporous, macroporous, or other specifically designed resins (such as reticulated, cross-linked polystyrene resins devoid of ionic function) and take up organics by a combination of ion exchange, adsorption, and other mechanisms. They typically are installed to precede the DI plant. 

The pore structure of most cross-linked polystyrene resins are the so called macro-reticular type which can be produced with almost any desired pore size, ranging from 20A to 5,000A. They exhibit strong dispersive type interaction with solvents and solutes with some polarizability arising from the aromatic nuclei in the polymer. Consequently the untreated resin is finding use as an alternative to the C8 and Cl8 reverse phase columns based on silica. Their use for the separation of peptide and proteins at both high and low pH is well established. 

The catalysts mentioned above are soluble. Certain cross-linked polystyrene resins, as well as alumina and silica gel, have been used as insoluble phase-transfer catalysts. These, called triphase catalysts, have the advantage of simplified product work up and easy and quantitative catalyst recovery, since the catalyst can easily be separated from the product by filtration. 

Devaky and Rajasree have reported the production of a polymer-bound ethylenediamine-borane reagent (63) (Fig. 41) for use as a reducing agent for the reduction of aldehydes.87 The polymeric reagent was derived from a Merrifield resin and a 1,6-hexanediol diacrylate-cross-linked polystyrene resin (HDODA-PS). The borane reagent was incorporated in the polymer support by complexation with sodium borohydride. When this reducing agent was used in the competitive reduction of a 1 1 molar mixture of benzaldehyde and acetophenone, benzaldehyde was found to be selectively reduced to benzyl alcohol. 

Numerous resin supports are commercially available for solid-phase synthesis and some allow the acquisition of quite reasonable quality spectra of compounds bonded to them - and some don t. The resins to avoid (if you intend trying to monitor your reactions by MAS-NMR) are any that are based purely on cross-linked polystyrene. These are too rigid and afford little or no mobility to any bound compound. These resins are relatively cheap and have high specific loadings but will give very poor spectra even in a MAS probe. We see little point in running spectra of compounds on these resins as the quality of the spectra make them virtually useless - and perhaps worse - potentially misleading. 

Use of benzene suspensions containing a neutral rhodium(I)-DIOP complex supported on a cross-linked polystyrene (50) (cf. 13 in Section III,A) for hydrogenation of a-ethylstyrene (to 1.5% ee) and methyl atro-pate (2.5% ee) was less effective than the homogeneous system, as the ethanol cosolvent required for substrate solubility caused a collapse of the resin (296). 

Assuming that the hydrophobic and nonionic nature of the polystyrene matrix prevented infiltration by solvent, an alternative synthesis was devised starting with macroporous 3% cross-linked polystyrene. This resin was first washed (28 ) with ... 

A number of modifications of the structure of the allylstannane have been prepared with the aim of facilitating the removal of tin from the product. These include Curran s fluorous allylstannane (see Section 3.14.04.1), Pereyre s monoallylstannane AllylXSn[N(TMS)2]2 (Equation (92) above),258 allylstannanes with a polar (oligoethylene oxide) tail (e.g., 23 and 24), and the allylstannyl group bonded to a soluble or insoluble (cross-linked) polystyrene. The reaction using the allylstannane bonded to a soluble, uncross-linked, polystyrene resin occurs about 100 times faster than that on the cross-linked, insoluble resin, and the polymer can be recovered by recrystallization from methanol. 

The separation takes place in a column of sulphonated cross-linked polystyrene resin, which is a strong cation exchanger. The matrix of the resin is strongly anionic in nature (S03 ) and at the low pH used initially, the amino acids will be positively charged and will be attracted to the negatively charged sulphonate groups. 

Spoly(vinylbenzylchloride). -Cross-linked using divinylbenzene. Chloromethylated, cross-linked polystyrene resins were obtained coiranercielly from Bio-Rad Laboratories. Percent chloromethylation js based on the available phenyl groups in the polymer that is minus the percent cross-linking. =D=dioxane E ethanol. Percent of available chloromethyl croups reacted with donor. —Percent reaction x percent chloromethylation. Polymer prepared by free-radical polymerization of 60.00 para-neta chloromethylated sytrene (Dow Chemical). Reaction heated at 50-55°C. 

Reversed-phase chromatography employs a nonpolar stationary phase and a polar aqueous-organic mobile phase. The stationary phase may be a nonpolar ligand, such as an alkyl hydrocarbon, bonded to a support matrix such as microparticulate silica, or it may be a microparticulate polymeric resin such as cross-linked polystyrene-divinylbenzene. The mobile phase is typically a binary mixture of a weak solvent, such as water or an aqueous buffer, and a strong solvent such as acetonitrile or a short-chain alcohol. Retention is modulated by changing the relative proportion of the weak and strong solvents. Additives may be incorporated into the mobile phase to modulate chromatographic selectivity, to suppress undesirable interactions of the analyte with the matrix, or to promote analyte solubility or stability. 

Citric acid separation from fermentation broth employs the full allotment of Sorbex beds in addition to the four basic Sorbex zones. The process utilizes a resin instead of a zeolite based adsorbent. The resin is a nonionic cross-linked polystyrene polyvinyl benzene formulation. Operating temperatures for this process are sufficient to overcome diffusion limitations with a corresponding operating pressure to maintain liquid-phase operation. The desorbent consists of water blended with acetone. Subsequent processing steps remove the desorbent from the desired extract product citric acid. 

Bio-beads consists of (1% cross-linked polystyrene with 1.25 mmol chloromethyl substitution per gram of dry resin respectively benzhydrylamine polymer (1% cross-linked polystyrene with 0.24 mmol NH2 per gram of dry resin, Bio-Rad Laboratories (Richmond, CA, USA). 

A key element in the original Merriheld procedure of solid-phase synthesis is the solid support system. That system consists of two parts a resin head and a. linker, an organic compound used to join the hrst amino acid to the resin head. The resin beads used by Merriheld are small spherical objects made of cross-linked polystyrene. This material consists primarily of the polymer polystyrene whose linear molecules are linked to each other at various positions by the addition of divinylhenzene (CH2 = CHCgH jCH =CH2). The hnal cross-linked material is relatively rigid, with enough hexihility to permit... 

Aiming at easier workup conditions, immobilization of several transition metal catalysts, which show activity for the epoxidation of allylic alcohols, on polymer support has been investigated. For example, Suzuki and coworkers incorporated an oxo-vanadium ion into cross-linked polystyrene resins functionalized with iminodiacetic acid or diethylenetri-amine derivatives (Scheme 57), which afforded a heterogeneous catalyst that can promote... 

The alternative strategy for heterogenization has been pursued by Blechert and co-workers, for a polymer-supported olefin metathesis catalyst. A polymer-anchored carbene precursor was prepared by coupling an alkoxide to a cross-linked polystyrene Merrifield-type resin. Subsequently, the desired polymer-bound carbene complex was formed by thermolytically induced elimination of ferf-butanol while heating the precursor resin in the presence of the desired transition metal fragment (Scheme 8.30). 

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