Third generation preparation

The third generation are latices made with independentiy prepared surfactant to mimic the in situ prepared functional monomer surfactant. These emulsifiers are often A—B block polymers where A is compatible with the polymer and B with the aqueous phase. In this way surface adsorption of the surfactant is more likely. These emulsions are known to exhibit excellent properties. 

When tetranuclear platinum complex (35) bridged by tetra(4-ethynylphenyl)-methane was used as the core (Fig. 6), dendrimers having more platinum atoms than those prepared from trinuclear platinum core 30 in the molecule were obtained up to the third generation. GPC analysis of these dendrimers revealed that the dendrimers with a tetraplatinum core have a similar molecular size to those with the triplatinum core 30. 

It is also possible to introduce polymerizable groups at the focal point of dendritic macromolecules and a number of authors have demonstrated the synthesis of novel hybrid dendritic-linear block copolymers by this methodology [69-73]. Initial experiments in the use of the dendritic macromonomers involved the preparation of a series of polyether dendrimers, such as the third generation derivative, 37, which contains a single styrene at its focal point [74]. Copolymerization of 37 with styrene then affords a hybrid block copolymer, 38, in which... 

Cefalexin is a first-generation cephalosporin and therefore an alternative preparation would be Zinnat tablets, which contains cefuroxime, a second-generation cephalosporin. A penicillin such as Augmentin, which contains co-amoxiclav, can be an appropriate alternative since it provides a very similar spectrum of activity. Klaricid contains clarithromycin, which is a macrolide. Utinor contains norfloxacin, which is a quinolone that is effective in uncomplicated urinary-tract infections. Rocephin contains ceftriaxone, which is a third-generation cephalosporin that is available for parenteral administration only. 

The so-called second generation ionic hquids were prepared from organic cations and AlCl anions [170]. Since AICI3 was present in these liquids, they were used as catalysts in Lewis acid catalyzed reactions. Also many of the third generation ionic liquids have been used as solvents for catalytic reactions [171-174], However, it is also known that third generation ionic liquids are capable of catalyzing reactions, either in substoichiometric amounts or as reaction medium. This will be discussed in this section. 

Application of the same dendrimer 31 in the Stille coupling of iodobenzene with tributylvinyltin in DMF (Scheme 10 5mol% catalyst) showed an activity equal to that of the tetraphosphole macrocycle complex (Fu3P)4Pd(OAc)2 (31b 100% conversion after 15 min). In contrast to the monomer, the dendritic catalyst could be recycled, but when recycled it showed a decrease in activity (95% conversion after 15 min). A better performance was achieved with the in situ prepared catalyst 32 by mixing the third-generation diphosphine dendrimer with Pd(OAc)2 (P/Pd ratio = 4/1). An activity similar to that of the monomeric complex (Fu3P)4Pd(OAc)2 was observed (100% conversion after 15 min), even after three consecutive runs. 

Similarly to the third generation Grubbs catalyst preparation, the related catalyst XXVI was obtained on addition of pyridine to precursor DC (Equation 8.6) [59]. 

Starting from ABB monomers, a multifunctionalised third-generation poly (benzyl ether) dendron could be prepared in which all eight terminal groups are... 

Up to third-generation ruthenium-carbene complexed dendrimers (Fig. 6.2) prepared by Astruc et al. contain a chelating diphosphane, which is sufficiently stable for construction of the dendritic architecture while also sufficiently reactive to permit synthesis of the dendrimer depicted in Fig. 6.3 by ring-opening metathesis polymerisation (ROMP) [3]. 

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