Polyester dendrimers

Polyamidoamine (PAMAM) dendrimers Polypropylene Imlne (PPI) dendrimers Polyester dendrimers Polylysine dendrimers... 

Yuan et al. [165] reported the synthesis of well-defined dendrimer-star, block-comb polymers by the combination of living ring-opening polymerization and atom transfer radical polymerization on the basis of a dendrimer polyester. Star-shaped dendrimer PCLs were synthesized by the bulk polymerization of e-caprolactone with a dendrimer initiator. The dendrimer PCLs tiien were converted into macroinitiators via esterification with 2-bromopropionyl bromide. And the star-block copolymer dendrimer poly(s-caprolactone)-block-poly(2-hydroxyethyl... 

Due to dieir compact, branched structure and to die resulting lack of chain entanglement, dendritic polymers exhibit much lower melt and solution viscosity dian their lineal" counterparts. Low a-values in die Mark-Houwink-Sakurada intrinsic viscosity-molar mass equation have been reported for hyperbranched polyesters.198 199 Dendrimers do not obey diis equation, a maximum being observed in die corresponding log-log viscosity-molar mass curves.200 The lack of chain entanglements, which are responsible for most of the polymer mechanical properties, also explains why hyperbranched polymers cannot be used as diermoplastics for structural applications. Aldiough some crystalline or liquid... 

However, dendrimeric and hyperbranched polyesters are more soluble than the linear ones (respectively 1.05, 0.70, and 0.02 g/mL in acetone). The solution behavior has been investigated, and in the case of aromatic hyperbranched polyesters,84 a very low a-value of the Mark-Houvink-Sakurada equation 0/ = KMa) and low intrinsic viscosity were observed. Frechet presented a description of the intrinsic viscosity as a function of the molar mass85 for different architectures The hyperbranched macromolecules show a nonlinear variation for low molecular weight and a bell-shaped curve is observed in the case of dendrimers (Fig. 5.18). 

The presence of a large number of chain-ends in the fully synthesized dendrimer molecules makes them highly soluble and also readily miscible, for example with other dendrimer solutions. The solubility is controlled by the nature of the end-groups, so that dendrimers with hydrophilic groups, such as hydroxyl or carboxylic acid, at the ends of the branches are soluble in polar solvents, whereas dendrimers with hydrophobic end-groups are soluble in non-polar solvents. The density of the end-groups at the surface of the dendrimer molecule means that they have proportionately more influence on the solubility than in linear polymers. Hence a dendritic polyester has been shown to be more soluble in tetrahydrofuran than an equivalent linear polyester. 

Nubbemeyer U (2001) Synthesis of Medium-Sized Ring Lactams. 216 125-196 Nummelin S, Skrifvars M, Rissanen K (2000) Polyester and Ester Functionalized Dendrimers. 210 1-67... 

The enzymatic polymerization of 12-hydroxydodecanoic acid in the presence of 11-methacryloylaminoundecanoic acid conveniently produced the methacrylamide-type polyester macromonomer. Lipases CA and CC were active for the macromonomer synthesis. Enzymatic selective monosubstitution of a hydroxy-functional dendrimer was demonstrated. Lipase CA-catalyzed polymerization of 8-CL in the presence of the first generation dendrimer gave the poly(8-CL)-monosubstituted dendrimer. 

Nummelin S, Skrifvars M, Rissanen K (2000) Polyester and Ester Functionalized Dendrimers. 

Preparation of Frechet-type Polyether Dendrons and Aliphatic Polyester Dendrimers by Convergent Growth An Experimental Primer... 

ALIPHATIC POLYESTER DENDRONS AND DENDRIMERS BASED ON 2,2-BIS-HYDROXYMETHYLPROPIONIC ACID... 

Dendrimers, or arborols, or cascade, or cauliflower, or starburst polymers, were first synthesized in the early 1980s [3,4]. In 1985 Tomalia et al. [5] and Newkome et al. [6] presented the first papers dealing with dendrimers. A multitude of dendrimers have been presented in the literature ranging from polyami-doamine [7,8],poly(propylene imine) [9,10], aromatic polyethers [11-13] and polyesters [14, 15], aUphatic polyethers [16] and polyesters [17], polyalkane [18-19], polyphenylene [20], polysilane [21] to phosphorus [22] dendrimers. Combinations of different monomers as well as architectural modifications have also been presented. For example, chirality has been incorporated in dendrimers [23,24]. Copolymers of linear blocks with dendrimer segments (dendrons) [25-27] and block-copolymers of different dendrons have been described [28]. 

An important application of polymers in medicine is in advanced drug-delivery systems. These materials control the drug concentration and delivery rate in the body. Hyperbranched polyesters have been suggested for such systems [111]. However, most applications within this field, described in the literature, deal with dendrimers and not with hyperbranched polymers. 

Fig. 13. Comparison of DSC traces for polyester dendrimers with phenolic and benzyloxy chain ends...

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