Structural Transitions of the Metal–Organic Framework DUT-49(Cu) upon Physi- and Chemisorption Studied by in Situ Electron Paramagnetic Resonance Spectroscopy

2020 ◽  
Vol 11 (15) ◽  
pp. 5856-5862
Author(s):  
Daniil M. Polyukhov ◽  
Simon Krause ◽  
Volodymyr Bon ◽  
Artem S. Poryvaev ◽  
Stefan Kaskel ◽  
...  
FEBS Letters ◽  
1991 ◽  
Vol 281 (1-2) ◽  
pp. 130-132 ◽  
Author(s):  
Ikuko Ueno ◽  
Satoshi Fujii ◽  
Hiroaki Ohya-Nishiguchi ◽  
Tetsutaro Iizuka ◽  
Shiro Kanegasaki

2017 ◽  
Vol 19 (46) ◽  
pp. 31030-31038 ◽  
Author(s):  
Anastasia Kultaeva ◽  
Timur Biktagirov ◽  
Jens Bergmann ◽  
Linda Hensel ◽  
Harald Krautscheid ◽  
...  

Successful combination of EPR and DFT was applied for investigation the novel heteronuclear MOF compounds.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Tian Luo ◽  
Lili Li ◽  
Yinlin Chen ◽  
Jie An ◽  
Chengcheng Liu ◽  
...  

AbstractConstruction of C-C bonds via reductive coupling of aldehydes and ketones is hindered by the highly negative reduction potential of these carbonyl substrates, particularly ketones, and this renders the formation of ketyl radicals extremely endergonic. Here, we report the efficient activation of carbonyl compounds by the formation of specific host-guest interactions in a hydroxyl-decorated porous photocatalyst. MFM-300(Cr) exhibits a band gap of 1.75 eV and shows excellent catalytic activity and stability towards the photoreductive coupling of 30 different aldehydes and ketones to the corresponding 1,2-diols at room temperature. Synchrotron X-ray diffraction and electron paramagnetic resonance spectroscopy confirm the generation of ketyl radicals via confinement within MFM-300(Cr). This protocol removes simultaneously the need for a precious metal-based photocatalyst or for amine-based sacrificial agents for the photochemical synthesis.


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