Photocatalytic C–H Activation with Alcohol as a Hydrogen Atom Transfer Agent in a 9-Fluorenone Based Metal–Organic Framework

Author(s):  
Zhonghe Wang ◽  
Le Zeng ◽  
Cheng He ◽  
Chunying Duan
2016 ◽  
Vol 7 (47) ◽  
pp. 7199-7203 ◽  
Author(s):  
Hui-Chun Lee ◽  
Markus Antonietti ◽  
Bernhard V. K. J. Schmidt

A Cu(ii) MOF can serve as an comprehensive catalyst for activators regenerated by electron transfer atom transfer radical polymerization (ARGET ATRP) in the synthesis of benzyl methacrylate, styrene, isoprene and 4-vinylpyridine.


2019 ◽  
Author(s):  
Chen-Hao Wang ◽  
Wen-Yang Gao ◽  
David Powers

We demonstrate that significant substrate confinement within a microporous Ru<sub>2</sub>-based MOF can be rationally tuned by modulating network mesoporosity. The reported data provide the first demonstration of tunneling during interstitial MOF chemistry and illustrate an experimental strategy to evaluate the impact of material structure on substrate mobility in porous catalysts.


2019 ◽  
Author(s):  
Chen-Hao Wang ◽  
Wen-Yang Gao ◽  
David Powers

We demonstrate that significant substrate confinement within a microporous Ru<sub>2</sub>-based MOF can be rationally tuned by modulating network mesoporosity. The reported data provide the first demonstration of tunneling during interstitial MOF chemistry and illustrate an experimental strategy to evaluate the impact of material structure on substrate mobility in porous catalysts.


2021 ◽  
Author(s):  
Jintong Liu ◽  
Jing Huang ◽  
Lei Zhang ◽  
Jianping Lei

We review the general principle of the design and functional modulation of nanoscaled MOF heterostructures, and biomedical applications in enhanced therapy.


2019 ◽  
Author(s):  
Shiori Date ◽  
Kensei Hamasaki ◽  
Karen Sunagawa ◽  
Hiroki Koyama ◽  
Chikayoshi Sebe ◽  
...  

<div>We report here a catalytic, Markovnikov selective, and scalable synthetic method for the synthesis of saturated sulfur heterocycles, which are found in the structures of pharmaceuticals and natural products, in one step from an alkenyl thioester. Unlike a potentially labile alkenyl thiol, an alkenyl thioester is stable and easy to prepare. The powerful Co catalysis via a cobalt hydride hydrogen atom transfer and radical-polar crossover mechanism enabled simultaneous cyclization and deprotection. The substrate scope was expanded by the extensive optimization of the reaction conditions and tuning of the thioester unit.</div>


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