Reversible Tuning Hydroquinone/Quinone Reaction in Metal-Organic Framework: Immobilized Molecular Switches in Solid State

被引:77
作者
Gui, Bo [1 ]
Meng, Xiangshi [1 ]
Chen, Yi [1 ]
Tian, Jianwu [1 ]
Liu, Guoliang [2 ]
Shen, Chencheng [1 ]
Zeller, Matthias [3 ]
Yuan, Daqiang [2 ]
Wang, Cheng [1 ]
机构
[1] Wuhan Univ, Coll Chem & Mol Sci, Minist Educ, Key Lab Biomed Polymers, Wuhan 430072, Peoples R China
[2] Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Peoples R China
[3] Youngstown State Univ, Dept Chem, Youngstown, OH 44555 USA
基金
高等学校博士学科点专项科研基金; 中国国家自然科学基金;
关键词
THIN-FILMS; ADSORPTION; CATALYSTS;
D O I
10.1021/acs.chemmater.5b02648
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Transferring the solution-state chemistry of organic-based molecular switches (OMS) into the solid state usually faces several fatal problems, such as spatial confinement or inefficient conversion. As a result, their switching behavior usually cannot be maintained. Herein, we report a redoxswitchable metal organic framework (MOF) that can undergo a reversible single-crystal-to-single-crystal (SCSC) transformation through a hydroquinone/quinone redox reaction. The redox-triggered transformation is quantitatively reversible while maintaining the crystallinity of the MOF scaffold. In addition, the transformation occurs gradually in the MOF backbone and from the outsurface of MOF to the inside. This study represents a general strategy to enable efficient conversion of the functionality of an OMS from solution into solid state, by incorporation of OMS into the framework of MOF. Furthermore, the material exhibits interesting changes in spectroscopic properties through reversible SCSC transformation and, thus, may be a starting point for the use of such materials in memory storage or redox-based electronic devices.
引用
收藏
页码:6426 / 6431
页数:6
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