Overcoming the crystallization and designability issues in the ultrastable zirconium phosphonate framework system

克服超稳定膦酸锆骨架系统中的结晶和可设计性问题

阅读:8
作者:Tao Zheng, Zaixing Yang, Daxiang Gui, Zhiyong Liu, Xiangxiang Wang, Xing Dai, Shengtang Liu, Linjuan Zhang, Yang Gao, Lanhua Chen, Daopeng Sheng, Yanlong Wang, Juan Diwu, Jianqiang Wang, Ruhong Zhou, Zhifang Chai, Thomas E Albrecht-Schmitt, Shuao Wang

Abstract

Metal-organic frameworks (MOFs) based on zirconium phosphonates exhibit superior chemical stability suitable for applications under harsh conditions. These compounds mostly exist as poorly crystallized precipitates, and precise structural information has therefore remained elusive. Furthermore, a zero-dimensional zirconium phosphonate cluster acting as secondary building unit has been lacking, leading to poor designability in this system. Herein, we overcome these challenges and obtain single crystals of three zirconium phosphonates that are suitable for structural analysis. These compounds are built by previously unknown isolated zirconium phosphonate clusters and exhibit combined high porosity and ultrastability even in fuming acids. SZ-2 possesses the largest void volume recorded in zirconium phosphonates and SZ-3 represents the most porous crystalline zirconium phosphonate and the only porous MOF material reported to survive in aqua regia. SZ-2 and SZ-3 can effectively remove uranyl ions from aqueous solutions over a wide pH range, and we have elucidated the removal mechanism.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。