Scholes Abbie M, Kershaw Cook Laurence J, Szczypiński Filip T, Luzyanin Konstantin V, Egleston Benjamin D, Greenaway Rebecca L, Slater Anna G
Department of Chemistry and Materials Innovation Factory, School of Physical Sciences, University of Liverpool UK
Department of Chemistry, Molecular Sciences Research Hub Imperial College London London UK.
Chem Sci. 2024 Aug 13;15(35):14254-63. doi: 10.1039/d4sc04207g.
Solid-state materials formed from discrete imine macrocycles have potential in industrial separations, but dynamic behaviour during both synthesis and crystallisation makes them challenging to exploit. Here, we explore opportunities for structural control by investigating the dynamic nature of a C-5 brominated isotrianglimine in solution and under crystallisation conditions. In solution, the equilibrium between the [3 + 3] and the less reported [2 + 2] macrocycle was investigated, and both macrocycles were fully characterised. Solvent templating during crystallisation was used to form new packing motifs for the [3 + 3] macrocycle and a previously unreported [4 + 4] macrocycle. Finally, chiral self-sorting was used to demonstrate how crystallisation conditions can not only influence packing arrangements but also shift the macrocycle equilibrium to yield new structures. This work thus exemplifies three strategies for exploiting dynamic behaviour to form isotrianglimine materials, and highlights the importance of understanding the dynamic behaviour of a system when designing and crystallising functional materials formed using dynamic covalent chemistry.
由离散亚胺大环形成的固态材料在工业分离方面具有潜力,但合成和结晶过程中的动态行为使其难以开发利用。在此,我们通过研究C-5溴化异三蝶烯亚胺在溶液中和结晶条件下的动态性质,探索结构控制的机会。在溶液中,研究了[3 + 3]大环与报道较少的[2 + 2]大环之间的平衡,并对这两种大环进行了全面表征。结晶过程中的溶剂模板作用被用于为[3 + 3]大环和一种以前未报道的[4 + 4]大环形成新的堆积模式。最后,利用手性自分类来证明结晶条件不仅可以影响堆积排列,还可以改变大环平衡以产生新结构。因此,这项工作例证了利用动态行为形成异三蝶烯亚胺材料的三种策略,并强调了在设计和结晶使用动态共价化学形成的功能材料时理解系统动态行为的重要性。