Kannaiyan Dinakaran, Imae Toyoko
Research Center for Materials Science, Nagoya University, Chikusa, Nagoya 464-8602, Japan.
Langmuir. 2009 May 5;25(9):5282-5. doi: 10.1021/la8039847.
Core-shell dendrimers consisting of poly(propyleneimine) (PPI) dendrimer as a core and poly(amidoamine) (PAMAM) dendrons as a shell have been synthesized through the route of Michael addition reaction followed by amidation. These macromolecules were investigated their ability to solubilize a guest molecule, pyrene. The number of encapsulated pyrene molecules per dendrimer increased with pH of a solution and generation (G) of PAMAM dendron, and it reached 2.7 for PPI(G3)-core:PAMAM(G3)-shell dendrimer at pH 11. It was confirmed that the solubilized pyrene located in the hydrophobic nanocavities of the PPI dendrimer core in the dendrimer. The shrunk PAMAM dendron shell should play a role of retention fence of doped molecules.
通过迈克尔加成反应后酰胺化的路线,合成了以聚(丙烯亚胺)(PPI)树枝状大分子为核、聚(酰胺胺)(PAMAM)树枝状分子为壳的核壳型树枝状大分子。研究了这些大分子溶解客体分子芘的能力。每个树枝状大分子包封的芘分子数随溶液pH值和PAMAM树枝状分子的代数(G)增加,在pH 11时,PPI(G3)核:PAMAM(G3)壳树枝状大分子达到2.7。证实了溶解的芘位于树枝状大分子中PPI树枝状大分子核的疏水纳米腔内。收缩的PAMAM树枝状分子壳应起到掺杂分子保留围栏的作用。