By M. Ballauf, R.M. Crooks, B.I. III Lemon, M. Möller (Contributors)
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Extra info for Topics in Current Chemistry 212, Dendrimers III Design, Dimersion, Function
2 Air Drying Coatings . . . . . . . . . . 2 Dyeable Polypropylene Fibers . . . . . . . . . . . 63 . . . . 63 . . . . 67 . . . . 68 6 Water Solubility and Future Developments . . . . . . . 4 Water Soluble Resins . . . . . . . . . . . . . Poly(ethyleneoxide) Functional Hyperbranched Polyesteramides Fluoroalkyl Functional Hyperbranched Polyesteramides . . Multifunctional Hyperbranched Polyesteramides . . . . 7 Conclusions 8 References . . . .
8 nm for dendrimer 55, which fits very well with our molecular mechanics calculation. AFM-measurements of the spin-coated alkyl-substituted dendrimers on HOPG also show the hexagonal arrangement of the dendrimers and confirm the dimensions obtained by X-ray diffraction. Core-shell dendrimers can also be synthesized by using a dendrimer as an initiator for polymerization, as core, and the polymers as shell [78, 79]. These polymers, often called star polymers, should have a broad range of applications, like stiffeners for polymeric materials  or high performance additives for adhesives, lube oils, and lubricants.
10 670 735 800 900 1040 1200 1500 1950 2700 1000 1060 1070 1160 1350 1540 1720 1810 2070 50 D. M. van Benthem mination of the exact degree of branching is also currently under investigation. , the molar mass. The glass transition temperatures determined with these polyesteramide resins appeared to be strongly dependent on the type of anhydride used and of their molecular weight. Figure 10 shows the dependence of glass transition temperature on molecular weight for hyperbranched polyesteramides based on hexahydrophthalic anhydride.