Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, Chang-Kung Chuang Institute , East China Normal University , 3663 N. Zhongshan Road , Shanghai 200062 , People's Republic of China.
Institute of Organic Chemistry and Biochemistry , Academy of Sciences of the Czech Republic , 16610 Prague 6 , Czech Republic.
J Am Chem Soc. 2019 Sep 4;141(35):13923-13930. doi: 10.1021/jacs.9b06739. Epub 2019 Aug 26.
Starting from a novel rotaxane building block with dendrimer growth sites being located at both the wheel and axle component, we realized the successful construction of a new family of rotaxane-branched dendrimers, i.e., Type III-C rotaxane-branched dendrimers, up to fourth generation as a highly branched [46]rotaxane through a controllable divergent approach. In the resultant rotaxane-branched dendrimers, the wheel components of the rotaxane units are located on the branches as well as at the branching points, making them excellent candidates to mimic the amplified collective molecular motions. Thus, taking advantage of the urea moiety inserted into the axle components of the rotaxane units as the binding sites, the addition or removal of acetate anion as stimulus endows the individual rotaxane unit a switchable feature that lead to a collective expansion-contraction motion of the integrated rotaxane-branched dendrimers, thus allowing for the remarkable and reversible size modulation. Such a three-dimensional size switching feature makes Type III-C rotaxane-branched dendrimers a very promising platform toward the fabrication of novel dynamic smart materials.
从一种新型轮烷砌块开始,其支化位点位于轮和轴组件上,我们通过可控发散方法成功构建了一类新型轮烷支化树状大分子,即第三代-C 型轮烷支化树状大分子,最高可达第四代作为高度支化的[46]轮烷。在所得的轮烷支化树状大分子中,轮烷单元的轮组件位于支链上以及支链点处,使它们成为模拟放大的集体分子运动的理想候选物。因此,利用插入轮烷单元轴组件中的脲部分作为结合位点,添加或去除乙酸根阴离子作为刺激赋予单个轮烷单元可切换的特征,导致集成的轮烷支化树状大分子的集体膨胀-收缩运动,从而允许进行显著和可逆的尺寸调节。这种三维尺寸切换特性使第三代-C 型轮烷支化树状大分子成为制造新型动态智能材料的极具前景的平台。