Hyperbranched materials chemical properties

Dendrimers are a class of macromolecules with a precisely controllable branched structure, consisting of three structural units a core, a hyperbranched scaffold and an external surface [16]. Dendrimers have been shown to possess unusual physical and chemical properties that differ significantly from those of linear oligomers and polymers. By using a fluorescent chromophore as the core of a dendrimer, one can apply fluorescence spectroscopy to study stmctural aspects and the conformational mobility of dendrimers in solution [17, 18]. At the same time, the dendritic shell provides a unique nanometer-sized environment for the spatial isolation of the chromophore, making them interesting materials for investigations by SMS. The synthesis of dendrimers with fluorescent chromophores attached to the rim serves as an efficient way to obtain a weU-defined number of chromophores in a confined volume [19-25]. Not only can the number of chromophores be easily controlled. 

The ultimate success of dendritic macromolecules as a new class of specialty polymer will depend on these novel materials possessing either new and/or improved physical, mechanical, or chemical properties when compared to standard linear polymers. In this article, the difference between dendrimers and their linear or hyperbranched analogs will be examined and the effect of these different architectures on physical properties discussed. 

Aromatic polyimides represent an important class of high-performance polymeric materials because of their many outstanding key properties, such as high mechanical strength, high modulus, unusual thermoxidative stability, excellent electrical properties, and superior chemical resistance [126,127]. Hyperbranched polyimides (hb-PIs) show high Tg and superior solubility due to their 3D architecture as well as excellent physical and chemical properties. 

Dendritic macromolecules exhibit compact globular structures which lead to their low viscosity in the melt or in solution. Furthermore, dendritic macromolecules are characterized by a very large number of available functional groups, which lead to unprecedented freedom for changing/tuning/tailoring the properties of these multivalent scaffolds via complete or partial derivatization with other chemical moieties. All these features have contributed to multidisciplinary applications of these unique macromolecular structures in recent years 6, 7). The development of efficient synthetic routes in recent years has given rise to a virtually unlimited supply of commercially available dendritic polymers, at very affordable price. The transport properties of hyperbranched and dendritic polymers have recently attracted attention as potentially new barrier and membrane materials 8-9). 

Due to their high molecular masses, macromolecular substances (polymers) show particular properties not observed for any other class of materials. In many cases, the chemical nature, the size, and the structure of these giant molecules result in excellent mechanical and technical properties. They can display very long linear chains, but also cyclic, branched, crosslinked, hyperbranched, and dendritic architectures as well. The thermoplastic behaviour or the possibility of crosslinking of polymeric molecules allow for convenient processing into manifold commodity products as plastics, synthetic rubber, films, fibres, and paints (Fig. 1.1). 

Type IV. Dendrimers and dendrons have perfectly and orderly branched tree-like structures. Their molecular mass increases with the growth of the number of generation. Dendrimers and dendrons, like common organic molecules, are perfectly controlled in terms of chemical structure, molecular mass, configuration and distribution of polymers [5]. Dendrons are well-ordered hyperbranched polymers and dendrimers are assembled from dendrons. It is expected that molecular-sized spaces between branched as well as hyperbranched polymers of dendrimers can be controlled and, therefore, could have high potential as gas separation membranes. An obvious disadvantage of dendrimers as membrane materials is their poor film-forming properties. 

M., From a Hyperbranched Polyethoxysiloxane Toward Molecular Forms of Silica A Polymer-Based Aproach to the Monitoring of Silica Properties. In Silicones and Silicone-Modified Materials, Clarson, S. J. Fitzgerald, J. J. Owen, M. J. Smith, S. D., Eds. American Chemical Society Washington, DC, 2000 Vol. 729, pp 503-515. 

Marija Pergal, MSc, works at the Department for Polymeric Materials, Institute for Chemistry, Technology and Metallurgy since 2003 as Research Scientist. Since 2007 she is also Teaching Assistant for the course Chemistry of Macromolecules at Department of Chemistry, University of Belgrade. Her research interests are focused on synthesis and characterization of siloxane homopolymers and copolymers, especially thermoplastic elastomers based on poly(butylene terephthalate) and polyurethanes, as well as polyurethane networks based on hyperbranched polyester. In addition to physico-chemical, mechanical and surface properties of polymers, her particular interest is directed towards the study of biocompatibility of polymer materials. 

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