Functionalization dendrimer

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... 

Fullerenes possess electronic and photophysical properties which make them natural candidates for the preparation of functional dendrimers. The attachment of a controlled number of dendrons on a core provides a compact insulating layer around the carbon sphere, and the... 

In these dye-functionalized dendrimers, light absorbed by the numerous peripheral coumarin-2 units is funneled to the coumarin-343 core with remarkably high efficiency (toluene solution 98% for the first three generations 93% for compound 8). Given the large transition moments and the good overlap between donor emission and acceptor absorption, energy transfer takes place by Forster mechanism [34]. 

A luminescent unit extensively used to functionalize dendrimers is the so-called dansyl (5-dimethylamino-l-naphthalenesulphonamido group). Dendrimers (up to the third generation, compound 9) containing a single dansyl unit attached off center [39] show that this fluorescent unit, which is very sensitive to environment polarity, is progressively shielded from interaction with water molecules as the dendrimer generation increases. 

This manuscript describes the dendritic macromolecules for optical and optoelectronic apph-cations, particularly stimulated emission, laser emission, and nonlinear optics. Dendrimers have been designed and synthesized for these applications based on simple concepts. A coreshell structure, through the encapsulation of active imits by dendritic branches, or a cone-shaped structure, through the step-by-step reactions of active imits, can provide particular benefits for the optical high-gain media and nonlinear optical materials. It also described experimental results that support the methods presented for designing and fabricating functionalized dendrimers for optoelectronic applications, and theoretical results that reveal the intermolecular electronic effect of the dendritic structure. 

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. 

E. K. Woller and M. J. Cloninger, The lectin-binding properties of six generations of mannose-functionalized dendrimers, Org. Lett., 4 (2002) 7-10. 

M. L. Wolfenden and M. J. Cloninger, Mannose/glucose-functionalized dendrimers to investigate the predictable tunability of multivalent interactions, J. Am. Chem. Soc., 127 (2005) 12168-12169. 

Figure 7.10 An NHS-PEG-maleimide compound can be used to functionalize dendrimers to provide a hydrophilic spacer terminating in thiol-reactive groups. Thiol-containing proteins then can be conjugated to this reactive intermediate to form covalent thioether bonds.

Shi, X., Wang, S., Sun, H., and Baker Jr., J.R. (2007) Improved biocompatibility of surface functionalized dendrimer-entrapped gold nanoparticles. Soft Matter 3, 71-74. 

Yoon, H.C., Lee, D., and Kim, H.-S. (2002) Reversible affinity interactions of antibody molecules at functionalized dendrimer monolayer affinity-sensing surface with reusability. Anal. Chim. Acta 456, 209-218. 

Another reaction performed in the dead-end reactor discussed before, is the allylic amination of 3-phenyl-2-propenyl-carbonic acid methyl ester with morpholine. [30] First and second generation commercially available DAB-dendrimers were functionalized with diphenylphosphine groups (Figure 4.13). Two different membranes were used, the Nadir UF-PA-5 (ultrafiltration) and the Koch MPF-50 (former SELRO) (nanofiltration), which gave retentions of 99.2% and 99.9% respectively for the second generation functionalized dendrimers. 

A non-covalently functionalized dendrimer was also applied in a continuous allylic amination reaction.[33] PPI dendrimers functionalized with urea adamantyl groups can act as host molecules for phosphorus ligands equipped with acetyl urea groups (Figure 4.18). The so formed supramolecular complex was reacted with a palladium precursor... 

Both the acid and ester were applied in continuous allylic amination. The maximum conversion (ca. 80%) was reached after 1 h in both experiments. Using the acid derivative of the guest, a slight drop in activity was observed ((a) in Figure 4.19), which is probably caused by a slow deactivation of the catalyst and has also been observed for covalently functionalized dendrimers (described above). When using the ester-functionalized guest, the activity dropped faster ((b) in Figure 4.19). This decrease in activity is caused by lack of retention (99.4% for the acid vs. 97% for the ester) as well as by deactivation. 

Figure 4.19. Continuous catalysis with non-covalently functionalized dendrimers a) acid-, b) ester-functionalized guest. (Reprinted with permission from ref. 33. Copyright 2001 American Chemical Society)...

A set of core-functionalized dendrimers was synthesized by Van Leeuwen et al. and one compound was applied in continuous catalysis. [45] The dendritic dppf, Xantphos and triphenylphosphine derivatives (Figures 4.22, 4.30 and 4.31) were active in rhodium-catalyzed hydroformylation and hydrogenation reactions (performed batch-wise). Dendritic effects were observed which are discussed in paragraph 4.5. The dendritic rhodium-dppf complex was applied in a continuous hydrogenation reaction of dimethyl itaconate. 

The same ligand system was used in the allylic alkylation of allyl trifluoroacetate with sodium diethyl-2-methylmalonate showing a more or less constant conversion over 8 h (20 exchanged reactor volumes). This is in contrast to peripheral functionalized dendrimers (Section 4.4.2), which deactivated at longer reaction times. 

Dendrimers are not only unreactive support molecules for homogeneous catalysts, as discussed in the previous paragraph, but they can also have an important influence on the performance of a catalyst. The dendrons of a dendrimer can form a microenvironment in which catalysis shows different results compared to classical homogeneous catalysis while peripheral functionalized dendrimers can enforce cooperative interactions between catalytic sites because of their relative proximity. These effects are called dendritic effects . Dendritic effects can alter the stability, activity and (enantio)selectivity of the catalyst. In this paragraph, different dendritic effects will be discussed. 

After a variety of very different dendrimers had become available up to high generations, many groups directed their attention more and more to designing and synthesizing functionalized dendrimers, i.e., dendrimers adorned with functionalities that are intended to give them characteristic properties favourable for application purposes.14,141... 

Generally, several different methods can be envisaged to obtain functionalized dendrimers. They include ... 

Structure controlled dendritic polymers that have been studied using gel electrophoresis generally behave as mimics of either proteins or nucleic acids, and possess similar ionic groups such as -NH3 , -COO , or P04 functionality. Dendrimer structures may be widely modified as a function of their interior composition and as well as the nature of their surface groups. Depending on their structure, the influence of pH may vary dramatically for different dendrimers. 

Its design versatility, as generic dendrons may be prepared to be used later as building blocks in conjunction with other reactive molecules, or coupled to a multifunctional core to afford functional dendrimers, dendritic-linear hybrids, dendronized polymers, etc. This may be a particularly significant advantage if the coupled reactive or core molecule is itself sensitive to the reaction conditions used in the multiple steps of the iterative synthesis of a dendrimer. 

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