Fang Yu, Xiao Zhifeng, Kirchon Angelo, Li Jialuo, Jin Fangying, Togo Tatsuo, Zhang Liangliang, Zhu Chengfeng, Zhou Hong-Cai
Department of Chemistry , Texas A&M University , College Station , Texas 77842-3012 , USA . Email:
Department of Chemistry , Faculty of Science , Kyushu University , 744 Motooka, Nishi-ku , Fukuoka , 819-0395 , Japan.
Chem Sci. 2019 Feb 9;10(12):3529-3534. doi: 10.1039/c8sc05315d. eCollection 2019 Mar 28.
The charge repulsion between a catalyst and substrate will significantly reduce the contact occurring between them, resulting in low reactivity. Herein, we report an anionic porous coordination cage that is capable of encapsulating both a cationic catalyst and cationic substrate in its cavity at the same time. After encapsulating the [Ru(bpy)]Cl (bpy = bipyridine) catalyst, the cage/catalyst composite serves as an active heterogeneous catalyst for the photo-degradation of methylene blue (MB). The highly negatively charged cavity of PCC-2 allows for the sequential encapsulation of the cationic methylene blue substrate and the Ru catalyst, which in turn significantly shortens the distance between them, yielding an increased possibility of MB degradation. Moreover, the encapsulated Ru catalyst dramatically outperformed its homogeneous counterpart in terms of overall degradation performance and recyclability.
催化剂与底物之间的电荷排斥会显著减少它们之间的接触,导致反应活性较低。在此,我们报道了一种阴离子多孔配位笼,它能够在其腔内同时包封阳离子催化剂和阳离子底物。包封[Ru(bpy)]Cl(bpy = 联吡啶)催化剂后,笼/催化剂复合材料作为一种活性多相催化剂用于亚甲基蓝(MB)的光降解。PCC-2高度带负电的腔允许阳离子亚甲基蓝底物和Ru催化剂依次包封,这反过来又显著缩短了它们之间的距离,增加了MB降解的可能性。此外,包封的Ru催化剂在整体降解性能和可回收性方面明显优于其均相对应物。