Covalent organic frameworks (COFs) formed by connecting multidentate organic building blocks through covalent bonds provide a platform for designing multifunctional porous materials with atomic precision. As they are promising materials for applications in optoelectronics, they would benefit from a maximum degree of long-range order within the framework, which has remained a major challenge. We have developed a synthetic concept to allow consecutive COF sheets to lock in position during crystal growth, and thus minimize the occurrence of stacking faults and dislocations. Hereby, the three-dimensional conformation of propeller-shaped molecular building units was used to generate well-defined periodic docking sites, which guided the attachment of successive building blocks that, in turn, promoted long-range order during COF formation. This approach enables us to achieve a very high crystallinity for a series of COFs that comprise tri- and tetradentate central building blocks. We expect this strategy to be transferable to a broad range of customized COFs.

Nature Chemistry (2016) doi:10.1038/nchem.2444

http://www.nature.com/nchem/journal/vaop/ncurrent/full/nchem.2444.html

中文报道链接（高度晶化的COF材料）：
http://mp.weixin.qq.com/s?__biz=MzA3NjIwODA1Nw==&mid=402069669&idx=5&sn=7ce681bb768129a9b609c9f5433f13f4&scene=0#wechat_redirect