Arborescent graft polymer

Gauthier, M. and Mdller, M. Uniform highly branched polymers hy anionic grafting Arborescent graft polymers. Macromolecules, 24, 4548, 1991. 

Figure 1 Macromolecular architectures linear macromolecular chains (homopolymer, block-copolymer and statistical copolymer [14]), brushed-polymer (= linear chains attached to a polymer-chain brush-polymer, brush-copolymers [14]), star polymer [4], mikto-star-polymer [16], arborescent graft polymer (=repeated grafting of linear chains on a macromolecule [17,18]), dendrimer (= maximally branched, regular polymer [15])...

IV. COMB-BURST DENDRIMER OR ARBORESCENT GRAFT POLYMERS... 

Winter, H.H. Evolution of rheology during chemical gelation. Prog. Colloid Polym. Scl,15,104—110,1987. Hempenius, M.A. et al. Melt rheology of arborescent graft polystyrenes. Macromolecules, 31, 2299, 1998. 

For the subsequent generation of arborescent graft polystyrenes, a dramatic increase in rj0 was observed by Hempenius et al. [43] for each of the three series included in their study. However, despite this increase in viscosity, the rj0 for each of these is still lower than that of the linear homologue polystyrenes of the same overall molecular weight. This jump in viscosity is due to an increase in branch density which in turn results in increase in chain extension similar to that observed by Roovers [31] for highly branched star polymers. 

Well-characterized systems. This depends on the appropriate chemistry and subsequent characterization (typical issues here are the polydispersity, control of grafting density, reproducibility of procedure to obtain identical particles). One frequent problem here is that the price one pays for such systems is tlie availability of small amounts (sometimes only fractions of 1 g) of material. For example, multiarm star polymers are in many ways unique, clean, soft colloids [ 19,23], but their nontrivial synthesis makes them not readily available. On the other hand, recent developments witli block copolymer micelles from anionically synthesized polymers [54-58] and arborescent graft copolymer synthesis [40] appear to have adequately addressed this issue for making available different alternative star-like systems. 

The effects of side chain architectures on the properties and proton conductivities of graft copolymer membranes for DMFCs were studied by Su et al. [126]. Poly(vinylidene fluoride)-g-poly(styrene sulfonic acid) (PVDF-g-PSSA) copolymers with either linear graft (LG) or arborescent graft (AG) PSSA side chains were prepared. Scheme 6.29 shows the structures of LG and AG polymers. 

Viville, R, Leclere, P., Deffieux, A. et al. (2004) Atomic force microscopy study of comb-like vs. arborescent graft copolymers in thin films. Polymer, 45,1833 1843. 

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