Photoactive Metal–Organic Framework for the Reduction of Aryl Halides by the Synergistic Effect of Consecutive Photoinduced Electron-Transfer and Hydrogen-Atom-Transfer Processes

2019 ◽  
Vol 12 (2) ◽  
pp. 2199-2206 ◽  
Author(s):  
Jiachen He ◽  
Jie Li ◽  
Qiuxia Han ◽  
Chen Si ◽  
Guiqin Niu ◽  
...  
Keyword(s):  
Electron Transfer ◽  
Hydrogen Atom ◽  
Synergistic Effect ◽  
Photoinduced Electron Transfer ◽  
Metal Organic Framework ◽  
Hydrogen Atom Transfer ◽  
Aryl Halides ◽  
Atom Transfer ◽  
Transfer Processes ◽  
Metal Organic

Sulfamides Direct Radical-Mediated Chlorination of Aliphatic C–H Bonds

2019 ◽  
Author(s):  
Melanie Short ◽  
Mina Shehata ◽  
Matthew Sanders ◽  
Jennifer Roizen
Keyword(s):  
Hydrogen Atom ◽  
Transfer Reaction ◽  
Hydrogen Atom Transfer ◽  
Chain Propagation ◽  
Propagation Mechanism ◽  
Atom Transfer ◽  
Radical Chain ◽  
Radical Intermediates ◽  
Transfer Processes ◽  
Unusual Position

Sulfamides guide intermolecular chlorine transfer to gamma-C(sp<sup>3</sup>) centers. This unusual position-selectivity arises because accessed sulfamidyl radical intermediates engage in otherwise rare 1,6-hydrogen-atom transfer processes. The disclosed chlorine-transfer reaction relies on a light-initiated radical chain-propagation mechanism to oxidize C(sp<sup>3</sup>)-H bonds.

Sulfamides Direct Radical-Mediated Chlorination of Aliphatic C–H Bonds

2019 ◽  
Author(s):  
Melanie Short ◽  
Mina Shehata ◽  
Matthew Sanders ◽  
Jennifer Roizen
Keyword(s):  
Hydrogen Atom ◽  
Transfer Reaction ◽  
Hydrogen Atom Transfer ◽  
Chain Propagation ◽  
Propagation Mechanism ◽  
Atom Transfer ◽  
Radical Chain ◽  
Radical Intermediates ◽  
Transfer Processes ◽  
Unusual Position

Sulfamides guide intermolecular chlorine transfer to gamma-C(sp<sup>3</sup>) centers. This unusual position-selectivity arises because accessed sulfamidyl radical intermediates engage in otherwise rare 1,6-hydrogen-atom transfer processes. The disclosed chlorine-transfer reaction relies on a light-initiated radical chain-propagation mechanism to oxidize C(sp<sup>3</sup>)-H bonds.

Selective chemochromic and chemically-induced photochromic response of a metal–organic framework

2020 ◽  
Vol 56 (44) ◽  
pp. 5929-5932 ◽  
Author(s):  
Peng Li ◽  
Qi Sui ◽  
Meng-Yue Guo ◽  
Shuai-Liang Yang ◽  
Ran Bu ◽  
...  
Keyword(s):  
Electron Transfer ◽  
Electron Acceptor ◽  
Photoinduced Electron Transfer ◽  
Color Change ◽  
Metal Organic Framework ◽  
Confined Space ◽  
Chemically Induced ◽  
Metal Organic ◽  
Organic Framework

The MOF provides unique confined space furnished with electron acceptor sites, and exposure to amines/alcohols causes specific and size-selective direct/UV-assisted color change owing to spontaneous/photoinduced electron transfer.

scholarly journals A Cu(ii) metal–organic framework as a recyclable catalyst for ARGET ATRP

2016 ◽  
Vol 7 (47) ◽  
pp. 7199-7203 ◽  
Author(s):  
Hui-Chun Lee ◽  
Markus Antonietti ◽  
Bernhard V. K. J. Schmidt
Keyword(s):  
Electron Transfer ◽  
Atom Transfer Radical Polymerization ◽  
Radical Polymerization ◽  
Metal Organic Framework ◽  
Recyclable Catalyst ◽  
Atom Transfer ◽  
Arget Atrp ◽  
Metal Organic ◽  
Organic Framework

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.

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