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Synergizing Steric Hindrance and Stacking Interactions To Facilitate the Controlled Assembly of Multiple 4 1 Metalla-Knots and Pseudo-Solomon Links.

Yan ZouShu-Jin BaoHaitong TangHai-Ning ZhangGuo-Xin Jin
Published in: Angewandte Chemie (International ed. in English) (2024)
In this work, a noncoplanar terphenyl served as a building block to synthesize a novel 3,3'-substituted bipyridyl ligand (L1) which further reacted with binuclear half-sandwich units A/B, giving rise to two aesthetic 4 1 metalla-knots in high yields via a coordination-driven self-assembly strategy. Furthermore, given the inherent compactness of the 4 1 metalla-knots, it creates favorable conditions for the emergence of steric repulsion. We focused on progressively introducing nitrogen atoms featuring a lone pair of electrons (LPEs) into ligand L1 to manipulate the balance of H⋅⋅⋅H/LPEs⋅⋅⋅LPEs steric repulsion during the assembly process, ultimately achieving controlled assembly from 4 1 metalla-knots to the pseudo-Solomon link and then to molecular tweezer-like assembly facilitated by stacking interactions. All the assemblies were well characterized by solution-state NMR techniques, ESI-TOF/MS, and single-crystal X-ray diffraction. The evolutionary process of the topological architectures is equivalent to visualizing the synergistic effect of steric hindrance and stacking interactions on structural assembly, providing a new avenue for achieving the controlled synthesis of different topologies.
Keyphrases
  • high resolution
  • ms ms
  • magnetic resonance
  • computed tomography
  • magnetic resonance imaging
  • dna methylation
  • molecular docking
  • genome wide
  • single molecule
  • mass spectrometry