Ballauff Matthias, Likos Christos N
Physikalische Chemie I, Universität Bayreuth, 95440 Bayreuth, Germany.
Angew Chem Int Ed Engl. 2004 Jun 7;43(23):2998-3020. doi: 10.1002/anie.200300602.
A variety of experimental and theoretical approaches show that, akin to linear polymers, dendrimers in good solvent conditions are best described as flexible macromolecular aggregates with a dense core and fluctuating monomer groups. We present theoretical and simulational evidence of how the shape and inner structure of dendrimers depends on the generation number as well as the effective interactions that exist between dendrimers in solution. These approaches based on simplified dendritic structures show there is a tunable and ultrasoft interaction between the centers of the solublized dendrimers. Results from small-angle neutron scattering data confirm the theory and indicate that dendrimers are model systems of ultrasoft colloids that bridge the gap between polymers and hard spheres. Dendrimers can form a class of materials analogous to the related systems of star polymers and block copolymer micelles which exhibit special properties.
多种实验和理论方法表明,与线性聚合物类似,在良好溶剂条件下的树枝状大分子最好被描述为具有致密核心和波动单体基团的柔性大分子聚集体。我们提供了理论和模拟证据,证明树枝状大分子的形状和内部结构如何取决于代数以及溶液中树枝状大分子之间存在的有效相互作用。这些基于简化树枝状结构的方法表明,溶解的树枝状大分子中心之间存在可调节的超软相互作用。小角中子散射数据的结果证实了该理论,并表明树枝状大分子是超软胶体的模型系统,填补了聚合物和硬球之间的空白。树枝状大分子可以形成一类类似于星形聚合物和嵌段共聚物胶束等相关体系的材料,这些体系具有特殊性质。