Shanghai Key Laboratory of Green Chemistry and Chemical Processes, Department of Chemistry, East China Normal University , Shanghai 200062, China.
J Am Chem Soc. 2015 Feb 4;137(4):1556-64. doi: 10.1021/ja511443p. Epub 2015 Jan 20.
Directed by increasing the density of coordination sites (DOCS) to increase the stability of assemblies, discrete 2D ring-in-rings and 3D sphere-in-sphere were designed and self-assembled by one tetratopic pyridyl-based ligand with 180° diplatinum(II) acceptors and naked Pd(II), respectively. The high DOCS resulted by multitopic ligand provided more geometric constraints to form discrete structures with high stability. Compared to reported supramolecular hexagons and polyhedra by ditotpic ligands, the self-assembly of such giant architectures using multitopic ligands with all rigid backbone emphasized the structural integrity with precise preorganization of entire architecture, and required elaborate synthetic operations for ligand preparation. In-depth structural characterization was conducted to support desired structures, including multinuclear NMR ((1)H, (31)P, and (13)C) analysis, 2D NMR spectroscopy (COSY and NOESY), diffusion-ordered NMR spectroscopy (DOSY), multidimensional mass spectrometry, TEM and AFM. Furthermore, a quantitative definition of DOCS was proposed to compare 2D and 3D structures and correlate the DOCS and stability of assemblies in a quantitative manner. Finally, ring-in-rings in DMSO or DMF could undergo hierarchical self-assembly into the ordered nanostructures and generated translucent supramolecular metallogels.
通过增加配位位点(DOCS)的密度来提高组装体的稳定性,设计并自组装了离散的二维环中环和三维球中球,分别由具有 180°二铂(II)受体和裸露钯(II)的四齿吡啶基配体。多齿配体提供的高 DOCS 为形成具有高稳定性的离散结构提供了更多的几何约束。与报道的由二齿配体形成的超分子六边形和多面体相比,使用具有全刚性骨架的多齿配体自组装这种巨大的结构强调了结构完整性,并且需要精心设计的配体制备合成操作。进行了深入的结构表征以支持所需的结构,包括多核 NMR((1)H、(31)P 和(13)C)分析、二维 NMR 光谱(COSY 和 NOESY)、扩散有序 NMR 光谱(DOSY)、多维质谱、TEM 和 AFM。此外,提出了 DOCS 的定量定义,以比较 2D 和 3D 结构,并以定量方式关联组装体的 DOCS 和稳定性。最后,DMSO 或 DMF 中的环中环可以进行分级自组装成有序的纳米结构,并生成半透明的超分子金属凝胶。