Dendrimer poly

Will these emerging megameric structures of poly(dendrimers) represent a new class of macromolecular architecture with unique properties and characteristics ... 

Tomalia-type poly(amidoamine) (PAMAM) dendrimers and their use as precise, fundamental building blocks to form poly(dendrimers) or so-called starburst polymers. These poly(dendrimers) are now referred to as megamers [35,36] and are described in more detail later. Other pioneers in the dendritic polymer field include Vogtle, New-kome, Frechet, and others. These historical contributions have been reviewed recently [33],... 

Some attention has arisen to consider dendrimers as building blocks for the construction of nanoarchitectures possessing higher complexity and dimensions beyond the dendrimer. In an early paper, Tomalia et al referred to their starburst polymers as a class of macromolecules obtained from the chemical bridging of starburst dendrimers. These macromolecules have been termed megamers, which have been defined as architectures derived from the combination of two or more dendritic macromolecules or poly(dendrimers). Many examples of randomly assembled as well as structure-controlled megamers have been reported, such as oligomeric covalent assemblies of dendrimers (i.e., dimers, trimers) referred... 

More recently, non-traditional polymerization strategies have evolved to produce a fourth new major polymer architecmral class, now referred to as dendritic polymers [43]. This new architectural polymer class consists of four major subsets (1) random hyperbranched, (2) dendrigrafts, (3) dendrons and (4) dendrimers. Dendrimers, the most extensively studied subset were discovered by the Tomalia group while in The Dow Chemical Company laboratories (1979) and represent the first example of synthetic, macromolecular dendritic architecture [43,44]. First use of the term dendrimer appeared in preprints for the first SPSJ International Polymer Conference, held in Kyoto, Japan in 1984 [45]. The following year, a full article in Polymer Journal [46] (Fig. 8) described the first preparation of a complete family of Tomalia-type poly(amidoamine) (PAMAM) dendrimers (G = 1-7) and their use as precise, fundamental building blocks to form poly (dendrimers) or so-called starburst polymers. These poly(dendrimers) are now referred to as megamers [47, 48] and are described in more detail later in Sect. 6.4.3. Other pioneers in the dendritic polymer field include Vogtle, Newkome, Frechet, Majoral, and others. These historical contributions have been reviewed recently [52]. ... 

Sebastian RM, Caminade AM, Majoial JP, LeviUain E, Huchet L, Roncah J (2000) Electrogenerated poly(dendrimers) containing conjugated poly(thiophene) chains. Chem Commun 507-508... 

Another possibility to immobilize the antibodies implies their direct attach onto electrode surfaces usually located as the walls of the microchannels. Different substrates can be used as electrode material. However, carbon derivatives, platinum, and mainly gold are the most used in microfluidic devices. An interesting possibility to immobilize biomolecules on the gold electrode surfaces within microchannels is through the use of monolayer of poly dendrimers. In the work or Park et the... 

Dendrimers have structures similar to that of hyperbranched polymer and can be taken as the perfectly branched polymer with monodispersity. However, they need to be prepared by a multistep procedure. Therefore, very little work has been done on dendritic polyfarylcnc ether)s. Morikawa et al. prepared a series of monomers with a various number of phenylene units.164,165 These monomer were used to prepare poly(ether ketone) dendrons with graded structures (Scheme 6.24). 

Nonetheless, it was a fairly short step from octopus compounds to dendrimers, and the step was taken by Vogtle in the late 1970s when he attempted to use a cascade reaction to prepare a molecule of the dendrimer type that would now be considered a dendron rather than a fully developed dendrimer. It began with the addition of acrylonitrile to an anfine, followed by reduction of the nitrile to amine. This was followed by a further reaction with acrylonitrile, and the process was repeated several times to yield highly branched macromolecules. There were initially problems with the reduction step but these were overcome, and the preparation of these poly(propylene imine) dendrimers was later commercialized. 

Synthetic pathways have been deliberately aimed at producing megamers. For example, poly(amido amine) dendrimers of different generations have been combined to give well-defined core-shell megamers in which a central, large core dendrimer is surrounded by a well-defined number of smaller dendrimers. 

Metal-acetylide complexes have been used as a unit of organometallic polymers that have metallic species in the main chain [20]. Representative examples are metal-poly(yne) polymers (19) of group 10 metals depicted in Scheme 5. These polymers are easily prepared from M(PR3)2Cl2 (M=Pt, Pd) and dialkynyl compounds catalyzed by Cu(I) salts in amine. Recently, this synthetic method was successfully applied to the construction of metal-acetylide dendrimers. 

Metal-acetylide complexes including metal-poly(yne) polymers often show unique properties [21-23]. Thus, metal-acetylide dendrimers are of interest because amplification of the functionality due to metal-acetylide units based on three-dimensional assembly with a regular dendritic structure is expected. 

Methanofullerene 20 with phenylacetylene dendrimer addends has also been reported [45] (Fig. 10). The UV absorption of fullerodendrimer 20 is particularly strong and is mainly attributed to transitions located on the two dendritic branches of the molecule. The photophysical investigations revealed that the large poly(aryl)acetylene branches act as photon antennae [46]. 

Fig. 13. Pseudorotaxane-terminated dendrimers from diaminobutane-functionalized poly-propylimine dendrimers and CB[6]...

Fig. 2. Poly(amidoamine) (PAMAM) dendrimers with carboxylate groups at the external surface...

The use of ordered supramolecular assemblies, such as micelles, monolayers, vesicles, inverted micelles, and lyotropic liquid crystalline systems, allows for the controlled nucleation of inorganic materials on molecular templates with well-defined structure and surface chemistry. Poly(propyleneimine) dendrimers modified with long aliphatic chains are a new class of amphiphiles which display a variety of aggregation states due to their conformational flexibility [38]. In the presence of octadecylamine, poly(propyleneimine) dendrimers modified with long alkyl chains self-assemble to form remarkably rigid and well-defined aggregates. When the aggregate dispersion was injected into a supersaturated... 

Anionic poly(amidoamine) (PAMAM) dendrimer was selected as a model of the soluble acidic-rich proteins to prepare CaC03 film on a poly(ethylenimine) film [49]. The CaCOj/polylethylenimine) composite film was obtained in the... 

Very interesting antenna systems have been constructed by functionalizing the chain ends of a poly(arylether) convergent dendritic backbone with cou-marin-2 A =435 nm) and its focal point with coumarin-343 X =49Q nm) [33] dendrimer 8 represents the fourth generation. 

Chiral dendrimers based on oligonaphthyl cores and Fr chet-type poly(aryl ether) dendrons have been investigated [44]. The absolute configuration of these dendrimers remains the same as that of their chiral cores. Both the nature of the core and the generation play a role in determining the fluorescence quantum yield. 

Poly(aryl ether) branches of generation 1 to 3 have been appended to a pho-totautomerizable quinoHne core to investigate the effect of dendritic architecture on the excited state intramolecular proton transfer [45]. The changes observed in the absorption and emission spectra on increasing dendrimer generation indicate that the dendritic branches affect the planarity of the core and therefore the efficiency of the excited state intramolecular proton transfer and of the related fluorescence processes. 

A poly(L-lysine) dendrimer 23 which carries 16 free-base porphyrins in one hemisphere and 16 Zn porphyrins in the other has been synthesized and studied in dimethylformamide solution [54]. In such a dendrimer, energy transfer from the Zn porphyrins to the free-base units can occur with 43% efficiency. When the 32 free base and zinc porphyrins were placed in a scrambled fashion, the efficiency of energy transfer was estimated to be 83% [55]. Very efficient (98%) energy transfer from Zn to free-base porphyrins was also observed in a rigid, snowflake-shaped structure in which three Zn porphyrin units alternate with three free-base porphyrin units [56]. 

That dendrimers are unique when compared with other architectures is confirmed by an investigation on porphyrin core dendrimers and their isomeric linear analogues [63]. The isomers displayed dramatically different hydrodynamic properties, crystallinity, and solubility characteristics when compared to those of their dendritic analogues, and photophysical studies showed that energy transfer from the poly(benzylether) backbone to the core was more efficient in the dendrimer because of the shorter distance between the donor units and the acceptor core. 

In a recent study, poly(aryl ether) dendritic branches terminated with triethyleneglycol chains were attached to Cgg [66] dendrimer 32 represents the fourth generation. The photophysical properties of these fullerodendrimers have been systematically investigated in three solvents, namely toluene, dichloromethane, and acetonitrile. On increasing dendrimer generation, it has been found that in each solvent (i) the maximum of the fullerene fluorescence band is red-shifted... 

Dye molecules can also be hosted into poly(propylene amine) dendrimers peripherally modified with OPV units [71]. In these systems, energy transfer from the OPV fluorescent units nm) to the enclosed dye molecules is... 

Dendritic hosts can be used in aqueous solution to encapsulate water-soluble fluorescent probes. Changes in the photophysical properties of these encapsulated probes are useful to understand the properties of the microenvironment created by the dendritic interior. For example, adamantyl-terminated poly(pro-pylene amine) dendrimers from the first to the fifth generation (36 represents the third generation) can be dissolved in water at pH<7 in the presence of -cyclodextrin because of encapsulation of the hydrophobic adamantyl residue inside the /1-cyclodextrin cavity and the presence of protonated tertiary amine units inside the dendrimer [72]. Under these experimental conditions, 8-anifi-... 

It has been demonstrated that dendrimers can be used also as fluorescent sensors for metal ions. Poly(propylene amine) dendrimers functionalized with dansyl units at the periphery like 34 can coordinate metal ions by the aliphatic amine units contained in the interior of the dendrimer [80]. The advantage of a dendrimer for this kind of application is related to the fact that a single analyte can interact with a great number of fluorescent units, which results in signal amplification. For example, when a Co ion enters dendrimer 34, the fluorescence of all the 32 dansyl units is quenched with a 32-fold increase in sensitivity with respect to a normal dansyl sensor. This concept is illustrated in Fig. 3. 

Fig. 2. A poly(phenylacetylene) dendrimer with an energy gradient across the conjugation length of the acetylene units from the periphery to the focal point...

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