Dendritic hyperbranched macromolecules

Dendritic and Hyperbranched Macromolecules -Precisely Controlled Macromolecular Architectures... 

A wide range of other monomer units have been employed in the synthesis of hyperbranched macromolecules and the range of structures obtained is nearly as diverse as those for dendritic macromolecules. For example, hyperbranched polyphenylenes [93], polyesters [104, 107-109], polyethers [110-112], polyamides [113], polysilanes [114], polyetherketones [100], polycarbazoles [115], etc. [116-118] have been prepared. Interestingly, a number of groups have also used growth processes other than condensation chemistry to prepare hyper-... 

While it can be expected that a number of physical properties of hyperbranched and dendritic macromolecules will be similar, it should not be assumed that all properties found for dendrimers will apply to hyperbranched macromolecules. This difference has clearly been observed in a number of different areas. As would be expected for a material intermediate between dendrimers and linear polymers, the reactivity of the chain ends is lower for hyperbranched macromolecules than for dendrimers [125]. Dendritic macromolecules would therefore possess a clear advantage in processes, which require maximum chain end reactivity such as novel catalysts. A dramatic difference is also observed when the intrinsic viscosity behavior of hyperbranched macromolecules is compared with regular dendrimers. While dendrimers are found to be the only materials that do not obey the Mark-Houwink-Sakurada relationship, hyperbranched macromolecules are found to follow this relationship, albeit with extremely low a values when compared to linear and branched polymers [126]. 

I personally wish to thank these authors for their time and effort to complete their contributions to this series and wish them continued success in their further endeavor in the field. Future volumes in this series will continue to highlight the research efforts of others in the field of cascade/dendritic and related hyperbranched macromolecules. 

Recently, dendrimers, which are hyperbranched macromolecules, were found to be an appropriate support for polymer catalysts, because chiral sites can be designed at the peripheral region of the dendrimers (Scheme 5). Seebach synthesized chiral dendrimer 14, which has TADDOLs on its periphery and used an efficient chiral ligand in the Ti(IV)-promoted enantioselective alkylation [21]. We developed chiral hyperbranched hydrocarbon chain 15 which has six p-ami-no alcohols [22], It catalyzes the enantioselective addition of diethylzinc to aldehydes. We also reported dendritic chiral catalysts with flexible carbosilane backbones [23]. 

Fig. 4.12 Examples of different dendritic architectures (a) hyperbranched macromolecule, (b) chemical structure of classic PAMAM dendrimer, repeat unit, and one full branch of generation GI (c) schematic of a backbone for generation G4. (From ref. [106])...

Hyperbranched and dendritic macromolecules have recently been the subject of considerable interest. Bolm developed chiral hyperbranched macromolecules 57 that catalyzed the enantioselective addition of diethylzinc to benzaldehyde [75]. The enan-tiocontrol of the hyperbranched chiral catalysts was slightly lower than for the low-molecular-weight catalyst. TADDOLs linked with dendritic molecules have been synthesized [59]. For example, use of the first generation dendrimer 58 with six terminal TADDOL units resulted in high enantioselectivity. 

Ishizu et al.194 synthesized hyperbranched macromolecules that resemble dendrimers. The synthetic approach involved the preparation of poly(4-methyl-styrene-b-PS-b-poly(4-methylstyrene) triblock copolymer by using naphthalene lithium as difunctional initiator. The 4-methyl groups of the terminal blocks were metalated with s-BuLi/tetramethylethylenedi-amine (TMEDA) complex in a molar ratio of 1 2. After removal of the excess s-BuLi by repeated precipitation of the living polymer and transfer of supernatant solution to another flask under high vacuum conditions, the polymer was dissolved in THF and was used as the initiator of a-methylstyrene at —78 °C. After the polymerization of a-methylstyrene, a small amount of 4-methylstyrene was added. The procedure of metalation of the a-methyl groups and polymerization of a-methylstyrene can be repeated many times to form a dendritic type hyperbranched polymer (Scheme 99). The characterization of the inter-... 

Hawker, C. J. Dendritic and hyperbranched macromolecules precisely controlled macromolecular architectures, Adv. Polym. Sci. 147, 113 (1999). 

Poly(ethylene oxide) (PEO) has been employed frequently as a water-soluble catalyst support [9]. Further water-soluble polymers investigated include other linear polymers such as poly(acrylic acid) [10], poly(N-alkylacrylamide)s [11], and copolymers of maleic anhydride and methylvinylether [12], as well as dendritic materials such as poly(ethyleneimin) [10a, c] or PEO derivatives of polyaryl ethers [13]. The term dendritic refers to a highly branched, tree-like structure and includes perfectly branched dendrimers as well as statistically branched, hyperbranched macromolecules. 

Dendritic and Hyperbranched Architectures. The first example of a PLL dendrimer synthesis vras patented hy Denkewalter et The authors described a divergent stepwise synthetic route starting from N -bis(Boc)-L-lysine benzhydrylamide. The dendritic macromolecule with a PDI close to 1 was built through repetitive coupling with a Boc-protected lysine derivative activated with p-nitrophenyl ester, followed by deprotection. Furthermore, dendritic PLL macromolecules were functionalized on the surface with arginine end-groups for insulin complexation. ... 

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