Wong Yip-Sang, Leung Frankie Chi-Ming, Ng Maggie, Cheng Heung-Kiu, Yam Vivian Wing-Wah
Institute of Molecular Functional Materials (Areas of Excellence Scheme, University Grants Committee (Hong Kong)) and Department of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong, People's Republic of China.
Angew Chem Int Ed Engl. 2018 Nov 26;57(48):15797-15801. doi: 10.1002/anie.201810302. Epub 2018 Nov 7.
The side-by-side assembly of gold nanorods (GNRs) was shown to be directed by the supramolecular scaffolds formed by sulfonate-containing alkynylplatium(II) terpyridine complexes. Driven by Pt⋅⋅⋅Pt and π-π stacking interactions, the Pt complex has a high propensity to assemble in water with the head-to-tail stacking arrangement to construct supramolecular scaffolds, in which the sulfonate groups on the terpyridine ligand at the peripheral position preferentially bind to the sides of the GNRs. The extent of the assembly of the GNRs into ladder rung-like nanostructures can be modulated by the concentration of the Pt complex. The Pt⋅⋅⋅Pt interaction-assisted formation of the scaffolds and its directed assembly of GNRs were characterized by UV/Vis spectroscopy, quantum-chemical modeling, electron microscopy, energy dispersed X-ray (EDX) analysis, and SERS. This work provides insights for the construction of higher-ordered nano-assemblies using both Pt⋅⋅⋅Pt interactions and template-directed approaches.
含磺酸基的炔基铂(II)三联吡啶配合物形成的超分子支架被证明可引导金纳米棒(GNR)的并排组装。在Pt⋅⋅⋅Pt和π-π堆积相互作用的驱动下,铂配合物在水中极易以头对头堆积排列进行组装,从而构建超分子支架,其中外围位置三联吡啶配体上的磺酸基团优先与GNR的侧面结合。GNR组装成梯级状纳米结构的程度可通过铂配合物的浓度进行调节。通过紫外/可见光谱、量子化学建模、电子显微镜、能量色散X射线(EDX)分析和表面增强拉曼光谱(SERS)对Pt⋅⋅⋅Pt相互作用辅助形成的支架及其对GNR的定向组装进行了表征。这项工作为利用Pt⋅⋅⋅Pt相互作用和模板导向方法构建高阶纳米组装体提供了思路。