Photoswitching storage of guest molecules in metal-organic framework for photoswitchable catalysis: exceptional product, ultrahigh photocontrol, and photomodulated size selectivity

被引:36
作者
Gong, Le Le [1 ,3 ]
Yao, Wan Ting [1 ]
Liu, Zhi Qiang [3 ]
Zheng, An Min [3 ]
Li, Jian Qiang [1 ]
Feng, Xue Feng [1 ]
Ma, Lu Fang [2 ]
Yan, Chang Sheng [1 ]
Luo, Ming Biao [1 ]
Luo, Feng [1 ]
机构
[1] East China Univ Technol, Sch Biol Chem & Mat Sci, State Key Lab Nucl Resources & Environm, Nanchang 344000, Jiangxi, Peoples R China
[2] Luoyang Normal Univ, Coll Chem & Chem Engn, Luoyang 471022, Peoples R China
[3] Chinese Acad Sci, Wuhan Inst Phys & Math, State Key Lab Magnet Resonance & Atom & Mol Phys, Wuhan 430071, Peoples R China
关键词
CARBON-DIOXIDE; COORDINATION POLYMERS; UPTAKE CAPACITY; NANOPARTICLES; ADSORPTION; CAPTURE; BEHAVIOR; LIGAND; CO2; POLYMERIZATIONS;
D O I
10.1039/c7ta01388d
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
MOF materials, as new catalysts, show high catalytic activity and size-, regio-, and stereo-selectivity. However, artificially controlling their catalytic process by convenient external stimulus such as light is still unexploited. Such photocontrol over an organic reaction may enable switchable catalytic activities and/ or selectivities, consequently producing desired products from a pool of building blocks according to the order and type of stimuli applied. In this study, we present a novel MOF catalyst, which not only offers ultrahigh photocontrol with the on/off ratio as high as 407, but also displays disparate photomodulation in reaction kinetics towards various aldehyde substrates in light of their sizes, thus creating the first example of MOFs showing photoswitchable catalysis. The origin, as unveiled by photoswitching adsorption experiments and density functional theory calculations, is due to photoswitching storage of guest molecules in the metal-organic framework (MOF).
引用
收藏
页码:7961 / 7967
页数:7
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