Zou Yan, Bao Shu-Jin, Tang Haitong, Zhang Hai-Ning, Jin Guo-Xin
State Key Laboratory of Molecular Engineering of Polymers, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Department of Chemistry, Fudan University, 2005 Songhu Road, Shanghai, 200438, P. R. China.
Angew Chem Int Ed Engl. 2024 Oct 1;63(40):e202410722. doi: 10.1002/anie.202410722. Epub 2024 Aug 20.
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 metalla-knots in high yields via a coordination-driven self-assembly strategy. Furthermore, given the inherent compactness of the 4 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 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.
在本工作中,一个非共平面的三联苯作为构建单元,用于合成一种新型的3,3'-取代联吡啶配体(L1),该配体进一步与双核半夹心单元A/B反应,通过配位驱动的自组装策略高产率地生成了两个美观的四核金属结。此外,鉴于四核金属结固有的紧凑性,它为空间排斥的出现创造了有利条件。我们专注于逐步将具有孤对电子(LPEs)的氮原子引入配体L1,以在组装过程中操纵H⋅⋅⋅H/LPEs⋅⋅⋅LPEs空间排斥的平衡,最终实现从四核金属结到伪所罗门链,再到由堆积相互作用促进的分子镊子状组装的可控组装。所有组装体均通过溶液态核磁共振技术、电喷雾飞行时间质谱(ESI-TOF/MS)和单晶X射线衍射进行了充分表征。拓扑结构的演化过程等同于可视化空间位阻和堆积相互作用对结构组装的协同效应,为实现不同拓扑结构的可控合成提供了一条新途径。