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Cgo bis-adducts

Fig. 29 Selective removal of bis (ethoxycarbonyl) methane addends in mixed Cgo bis-adducts. Fig. 29 Selective removal of bis (ethoxycarbonyl) methane addends in mixed Cgo bis-adducts.
Polymer 16 was synthesized through a poly-SNA reaction between the commercially available aminopropyl-end-capped-PDMS 15 (M 35000) and a mixture of Cgo-bis adducts 14, which was in turn prepared by the o-xylylene method [15]. After SEC purificahon, the resulting material presented a high average molecular weight (>50000) and a of 150000. [Pg.18]

Dendrimers 5-8 were obtained by taking advantage of the versatile regiose-lective reaction developed in the group of Diederich [24], which led to macro-cyclic bis-adducts of Cgg by a cyclization reaction at the C sphere with bis-mal-onate derivatives in a double Bingel cyclopropanation [25]. Reaction of the dendritic malonates with Cgg, I2, and l,8-diazabicyclo[5.4.0]undec-7-ene (DBU) in toluene at room temperature afforded the corresponding cyclization products 5-8 (Fig. 2). The relative position of the two cyclopropane rings in 5-8 on the Cgo core was determined based on the molecular symmetry deduced from the and NMR spectra (Cs) as well as on their UV/Vis spectra. It is well estabhshed... [Pg.89]

The scope of the tether-directed remote functionalization has been expanded from Cgo to the higher fullerene C70, and the described reactions are completely regioselective, featuring, in the case of C70, the kinetically disfavored addition pattern. The crown ether is a real template, since it can be readily removed by transesterification, giving a much-improved access to certain bis-adducts that are not accessible by the direct route. Cation-binding studies by CV reveal that cyclophane-type crown ethers derived from C60 and C70 form stable complexes with metal cations, and a perturbation of the fullerene reduction potentials occurs because the cation is tightly held close to the fullerene surface. This conclusion is of great importance for future developments of fullerene-based electrochemical ion sensors. [Pg.167]

Figure 1.19. Chiral bis-adducts of Cgo obtained by tether-directed cycloaddition reactions. Figure 1.19. Chiral bis-adducts of Cgo obtained by tether-directed cycloaddition reactions.

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See also in sourсe #XX -- [ Pg.71 , Pg.72 , Pg.73 , Pg.74 , Pg.75 ]




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