Guo Dong-Sheng, Chen Kun, Zhang Hong-Qing, Liu Yu
Department of Chemistry, State Key Laboratory of Elemento-Organic Chemistry, Nankai University, Tianjin, 300071, PR China.
Chem Asian J. 2009 Mar 2;4(3):436-45. doi: 10.1002/asia.200800410.
Possessing 2D netlike and 1D linear morphologies, two nano-supramolecular architectures A1 and A2 are constructed by tetracationic porphyrin (G1) and dicationic porphyrin (G2), respectively, upon complexation with the novel water-soluble bis(p-sulfonatocalix[5]arenes) bridged at the lower rim (H2). Corresponding to the molecular design, the aggregation morphologies are well manipulated by the inherent binding sites of the building blocks through host-guest interactions as well as charge interactions. In comparison to the simple p-sulfonatocalix[5]arene H1 which can only form particle-type complexes C1 and C2 with porphyrin guests, H2 provides excellent pre-organized structure to construct highly complex nano-supramolecular assemblies. The exhibited electron-transfer process of the supramolecular systems is further investigated by steady-state and time-resolved fluorescence spectroscopy, electrochemical measurements, and transient absorption spectroscopy. The results obtained show that calixarenes are also effective electron donors in PET besides acting as significant building blocks, which gives them many advantages in constructing well-ordered nanomaterials with the capability of electron and energy transport.
通过四价阳离子卟啉(G1)和二价阳离子卟啉(G2)分别与在下缘桥连的新型水溶性双(对磺酸钠杯[5]芳烃)(H2)络合,构建了具有二维网状和一维线性形态的两种纳米超分子结构A1和A2。与分子设计相对应,聚集形态通过主客体相互作用以及电荷相互作用,由构建块的固有结合位点很好地控制。与只能与卟啉客体形成颗粒型配合物C1和C2的简单对磺酸钠杯[5]芳烃H1相比,H2提供了优异的预组织结构以构建高度复杂的纳米超分子组装体。通过稳态和时间分辨荧光光谱、电化学测量以及瞬态吸收光谱进一步研究了超分子体系中表现出的电子转移过程。所得结果表明,杯芳烃除了作为重要的构建块外,还是PET中有效的电子供体,这使其在构建具有电子和能量传输能力的有序纳米材料方面具有许多优势。