以收斂型的合成方法,合成出一系列中心核為triazine、末端基為dioctyl的樹枝狀高分子(GnNH,n=1,2,3,4)。將此樹枝狀高分子末端的連接基進行改質,產生兩種不同連接基的樹枝狀高分子:GnSH (n=1,2,3,4)和GnCOOH (n=1,2,3)。 在含有硫醇基(-SH)的樹枝狀高分子存在下,sodium borohydride當還原劑,用Brust兩相法(水-甲苯)來還原AuCl4-,形成表面由含有硫醇基(-SH)的樹枝狀高分子包覆的金奈米粒子溶液。經由穿隧式電子顯微鏡,可得知此奈米粒子的粒徑在3~5 奈米。 含有羧基(-COOH)的樹枝狀高分子經由偏光顯微鏡觀察後,沒有發現有液晶的性質。因此,將此樹枝狀高分子與八種不同的配子混合成氫鍵型複合物,經由偏光顯微鏡觀察,也沒有發現液晶的性質。
A series of dendrimer (GnNH, n=1, 2, 3, 4), using triazine as central cores and dioctylamine as terminal functionalitie were prepared by a convergent method. Two functional dendrimers (GnSH and GnCOOH) were prepared by reaction of terminal linking group of GnNH with gamma-thiobutyrolacton or maleic anhydride. Using Brust’s two phase (water-toluene) reduction of AuCl4- by sodium borohydrid in the presence of a mercapto-containing dendrimer, solutions of gold nanoparticle bearing a surface coating of mercapto-containing dendrimer have been prepared. By TEM (Transmission Electron Microscopy) analyses, the nanoparticle diameters were measured to be 3~5 nm approximately. 英文摘要 By POM (Polarized Optical Microscope) analyses, all carboxyl-containing dendrimer does not show any mesogenic phase. Also, hydrogen bonding complexes from carboxyl-containing dendrimer and eight different porton acceptors does not show any mesogenic phase.