Han Ming, Liu Yuwei, Qian Dong-Jin, Lee Yong-Ill, Liu Hong-Guo
Key Laboratory for Colloid and Interface Chemistry of Education Ministry, Shandong University, Jinan 250100, P. R. China.
Department of Chemistry, Fudan University, Shanghai 200438, P. R. China.
Langmuir. 2021 Apr 20;37(15):4515-4522. doi: 10.1021/acs.langmuir.0c03670. Epub 2021 Apr 6.
Two-dimensional functional metal-organic frameworks and coordination polymers have attracted much attention and have been successfully prepared in solutions and at interfaces through the coordination of ligands to metal ions. However, the preparation of large-area ultrathin ordered films is still a challenge. Here, a modified liquid/liquid interfacial epitaxial growth method has been developed. A planar liquid/liquid interface between a chloroform solution of bipyridine derivatives and pure water was constructed first, and then an aqueous solution of Eu or Cu ions was added dropwise into the water phase. A layered ultrathin film with the size of several hundreds of square micrometers appeared at the liquid/liquid interface after a certain time. The monitoring results showed that the formation of ultrathin films was a result of continuous epitaxial growth of the adsorbed species due to the synergistic effects of hydrophobic effects of the alkyl chains, coordination bonds between the ligands and metal ions, π-π interactions between the ligands, and the restriction of the interface on the vertical growth. This offers a way to fabricate more large-area thin films of amphiphilic molecules.
二维功能金属有机框架和配位聚合物已引起广泛关注,并已通过配体与金属离子的配位作用在溶液和界面上成功制备。然而,大面积超薄有序薄膜的制备仍然是一个挑战。在此,已开发出一种改进的液/液界面外延生长方法。首先构建联吡啶衍生物的氯仿溶液与纯水之间的平面液/液界面,然后将铕或铜离子的水溶液滴加到水相中。一段时间后,在液/液界面出现了尺寸为数百平方微米的层状超薄膜。监测结果表明,超薄膜的形成是由于烷基链的疏水作用、配体与金属离子之间的配位键、配体之间的π-π相互作用以及界面在垂直生长上的限制等协同效应,使得吸附物种持续外延生长的结果。这为制备更多两亲分子的大面积薄膜提供了一种方法。