Ibáñez Susana, Vicent Cristian, Peris Eduardo
Institute of Advanced Materials (INAM), Universitat Jaume I, Av. Vicente Sos Baynat s/n, 12071, Castellón, Spain.
Servei Central d'Instrumentació Científica (SCIC), Universitat, Jaume I, Avda. Sos Baynat s/n, 12006, Castellón, Spain.
Angew Chem Int Ed Engl. 2022 Jan 10;61(2):e202112513. doi: 10.1002/anie.202112513. Epub 2021 Nov 25.
In this study we report the preparation of a new mechanically interlocked molecule formed by the self-aggregation of two metallotweezers composed by two pyrene-imidazolylidene gold(I) arms and a pyridine-centered pentacyclic bis-alkynyl linker. The mechanically interlocked nature of this molecule arises from the presence of the bulky tert-butyl groups attached to the sides of the pyrene moieties of the arms of the tweezer, which act as stoppers avoiding the dissociation of the self-aggregated metallotweezer dimer once it is formed. By combining experimental techniques, we were able to confirm the mechanically interlocked nature of this molecule in solution, in the gas phase and in the solid state. The behavior of the tert-butyl substituted tweezer differs greatly form that shown by the tweezer lacking of these bulky groups, whose dimeric structure is in equilibrium with the monomeric structure, therefore not showing any mechanical coercion that avoids the disassembly of the self-aggregated structure.
在本研究中,我们报道了一种新的机械互锁分子的制备,该分子由两个金属镊子自聚集形成,每个金属镊子由两个芘-咪唑亚基金(I)臂和一个以吡啶为中心的五环双炔基连接体组成。该分子的机械互锁性质源于连接在镊子臂芘部分侧面的庞大叔丁基的存在,这些叔丁基起到塞子的作用,一旦自聚集金属镊子二聚体形成,就可避免其解离。通过结合实验技术,我们能够在溶液、气相和固态中证实该分子的机械互锁性质。叔丁基取代的镊子的行为与缺乏这些庞大基团的镊子的行为有很大不同,后者的二聚体结构与单体结构处于平衡状态,因此没有表现出任何避免自聚集结构拆解的机械强制作用。