Self-Assembly of Supramolecular Fractals from Generation 1 to 5

In the seeking of molecular expression of fractal geometry, chemists have endeavored in the construction of molecules and supramolecules during the past few years, while only a few examples were reported, especially for the discrete architectures. We herein designed and constructed five generations...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of the American Chemical Society 2018-10, Vol.140 (43), p.14087-14096
Hauptverfasser: Wang, Lei, Liu, Ran, Gu, Jiali, Song, Bo, Wang, Heng, Jiang, Xin, Zhang, Keren, Han, Xin, Hao, Xin-Qi, Bai, Shi, Wang, Ming, Li, Xiaohong, Xu, Bingqian, Li, Xiaopeng
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:In the seeking of molecular expression of fractal geometry, chemists have endeavored in the construction of molecules and supramolecules during the past few years, while only a few examples were reported, especially for the discrete architectures. We herein designed and constructed five generations of supramolecular fractals (G1–G5) based on the coordination-driven self-assembly of terpyridine ligands. All the ligands were synthesized from triphenylamine motif, which played a central role in geometry control. Different approaches based on direct Sonogashira coupling and/or ⟨tpy-Ru­(II)-tpy⟩ connectivity were employed to prepare complex Ru­(II)-organic building blocks. Fractals G1–G5 were obtained in high yields by precise coordination of organic or Ru­(II)-organic building blocks with Zn­(II) ions. Characterization of those architectures were accomplished by 1D and 2D NMR spectroscopy, electrospray ionization mass spectrometry (ESI-MS), traveling-wave ion mobility mass spectrometry (TWIM-MS), and transmission electron microscopy (TEM). Furthermore, the two largest fractals also hierarchically self-assemble into ordered supramolecular nanostructures either at solid/liquid interface or in solution on the basis of their well-defined scaffolds.
ISSN:0002-7863
1520-5126
DOI:10.1021/jacs.8b05530