Silica supported dendrimers

The use of heterogeneous catalysts in this reaction has also been achieved palladium-montmorillonite clays [93] or palladium/activated carbon [94] in the presence of dppb transformed 2-allylphenols into lactones, the regiose-lectivity of the reaction being largely dependant on the nature of the support. Very recently, palladium complexes immobilized onto silica-supported (polyaminoamido)dendrimers were used as catalysts in the presence of dppb for the cyclocarbonylation of 2-allylphenols, 2-allylanilines, 2-vinylphenols, and 2-vinylanilines affording five-, six-, or seven-membered lactones and lactams. Good conversions are realized and the catalyst can be recycled 3-5 times [95]. 

S. D. Deutsch, et al, Decomposition and activation of Pt-dendrimer nanocomposites on a silica support, Catal Lett. 97, 139-143 (2004). 

Similar 0—4 generations silica-supported Pd-PAMAM dendrimers with various spacer lengths were used by Alper et al. as recyclable catalysts for the hydroesterification reaction of alkenes (55) and the oxidation of terminal alkenes to methyl ketones (56). The hydroesterification experiments (Scheme 16) showed that (PPh3)2Pd-PPh2-PAMAM-Si02 complexes were highly active catalysts for styrene derivatives and linear long-chain alkenes (numbers of turnovers up to 1200). 

In a subsequent paper, the authors developed another type of silica-supported dendritic chiral catalyst that was anticipated to suppress the background racemic reaction caused by the surface silanol groups, and to diminish the multiple interactions between chiral groups at the periphery of the dendrimer 91). The silica-supported chiral dendrimers were synthesized in four steps (1) grafting of an epoxide linker on a silica support, (2) immobilization of the nth generation PAMAM dendrimer, (3) introduction of a long alkyl spacer, and (4) introduction of chiral auxiliaries at the periphery of the dendrimer with (IR, 2R)-( + )-l-phenyl-propene oxide. Two families of dendritic chiral catalysts with different spacer lengths were prepared (nG-104 and nG-105). 

In another example of the dendronization of solid supports, Rhee et al. described the design of silica-supported chiral dendritic catalysts for the en-antioselective addition of diethylzinc to benzaldehyde (Fig. 28) [60-62], The immobilized dendritic systems were formed in two different ways one by stepwise propagation of dendrimers and the other by direct immobilization... 

Fig. 29 Effect of the linker chain lengths on the intermolecular interaction of catalytic dendrimers immobilized on silica supports [62]...

Soluble dendrimers bearing catalytic centers located at the periphery can be covalently attached onto the surface of conventional solid supports (such as polymer beads or silica gels), leading to another type of solid-supported dendrimer catalyst. It is expected that this type of immobihzed catalysts would combine the advantages of both the traditional supported catalysts and the dendrimer catalysts. First, the catalytically active species at the dendrimer surface are more easily solvated, which makes the catalytic sites more available in the reaction solutions (relative to cross-hnked polymers). Second, the insoluble supported dendrimers are easily removed from the reaction mixtures as precipitates or via filtration (relative to soluble dendrimers). These solid-supported peripheraUy functionalized chiral dendrimer catalysts have attracted much attention over the past few years [12, 113], but their number of applications in asymmetric catalysis is very limited. 

Figure 4.43 Silica-supported chiral dendrimers bearing ephedrine moieties located at the periphery.

PtNPs and bimetallic dendrimer-stabilized Pd-AuNPs were adsorbed onto a high-surface silica support and thermally activated to remove the dendrimers... 

M.R Ottaviani, R. Valluzzi, L. Balogh, Internal Structure of SUver-Poly(amidoam-ine) Dendrimer Complexes and Nanocomposites, Macromolecules 35, 5105, 2002. D.S. Deutsch, G. Lafaye, D. Liu, B.D. Chandler, C.T. Williams, M.D. Amiridis, Decomposition and Activation of Pt-Dendrimer Nanocomposites on a Silica Support, Catalysis Letters 97, 139, 2004. 

The solvent, toluene, plays an important role in the leaching-inhibition mechanism of the silica-supported Pt DENs catalyst. Since toluene is a nonpolar solvent, the Pt ions prefer to stay in the polar environment inside the PAMAM dendrimers... 

Castillo VA, Kuhn JN (2012) Role of the Ni Fe ratio in ethylene hydrogenation activity for silica-supported Ni-Fe clusters prepared by dendrimer-templating. J Phys Chem C 116 8627... 

Although beyond the scope of this book, a vast amount of work has been directed to supporting homogeneous catalysts on solid supports including silica, alumina and zeolites, and functionalized dendrimers and polymers [19]. These give rise to so-called solid-liquid biphasic catalysis and in cases where the substrate and product are both liquids or gases then co-solvents are not always required. In many ways solvent-free synthesis represents the ideal method but currently solvent-free methods can only be applied to a limited number of reactions [20],... 

Immobilizing DENs within a sol-gel matrix is another potential method for preparing new supported catalysts. PAMAM and PPI dendrimers can be added to sol-gel preparations of silicas " and zinc arsenates to template mesopores. In one early report, the dendrimer bound Cu + ions were added to sol-gel silica and calcined to yield supported copper oxide nanoparticles. Sol-gel chemistry can also be used to prepare titania supported Pd, Au, and Pd-Au nanoparticle catalysts. Aqueous solutions of Pd and Au DENs were added to titanium isopropoxide to coprecipitate the DENs with Ti02. Activation at 500°C resulted in particles approximately 4 nm in diameter. In this preparation, the PAMAM dendrimers served two roles, templating both nanoparticles and the pores of the titania support. 

There are reports of numerous examples of dendritic transition metal catalysts incorporating various dendritic backbones functionalized at various locations. Dendritic effects in catalysis include increased or decreased activity, selectivity, and stability. It is clear from the contributions of many research groups that dendrimers are suitable supports for recyclable transition metal catalysts. Separation and/or recycle of the catalysts are possible with these functionalized dendrimers for example, separation results from precipitation of the dendrimer from the product liquid two-phase catalysis allows separation and recycle of the catalyst when the products and catalyst are concentrated in two immiscible liquid phases and immobilization of the dendrimer in an insoluble support (such as crosslinked polystyrene or silica) allows use of a fixed-bed reactor holding the catalyst and excluding it from the product stream. Furthermore, the large size and the globular structure of the dendrimers enable efficient separation by nanofiltration techniques. Nanofiltration can be performed either batch wise or in a continuous-flow membrane reactor (CFMR). 

The focus of these studies has been on identifying mild activation conditions to prevent nanoparticle agglomeration. Infrared spectroscopy indicated that titania plays an active role in dendrimer adsorption and decomposition in contrast, adsorption of DENs on silica is dominated by metal-support interactions. Relatively mild (150° C) activation conditions were identified and optimized for Pt and Au catalysts. Comparable conditions yield clean nanoparticles that are active CO oxidation catalysts. Supported Pt catalysts are also active in toluene hydrogenation test reactions. 

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