ChemInform Abstract: Copper Catalyzed Oxidative Alkylation of sp3 C—H Bond Adjacent to a Nitrogen Atom Using Molecular Oxygen in Water.

ChemInform ◽  
2008 ◽  
Vol 39 (8) ◽  
Author(s):  
Olivier Basle ◽  
Chao-Jun Li
1993 ◽  
Vol 58 (2) ◽  
pp. 354-364 ◽  
Author(s):  
Jaroslav Burda ◽  
Božena Lánská

The radical-initiated chain oxidation of five- to nine-membered lactams with molecular oxygen has been studied by the quantum-chemical method AM1. It has been confirmed that the reaction is controlled by its propagation step. The kinetic length of the oxidation chains correlates with the energy of formation of the lactam radical by abstraction of hydrogen from the methylene group adjacent to nitrogen atom. With five- to eight-membered rings the reaction is symmetry-forbidden.


2015 ◽  
Vol 60 (1) ◽  
pp. 46-51 ◽  
Author(s):  
I.P. Koval ◽  
◽  
Yu.A. Len ◽  
M.G. Nakhodkin ◽  
M.O. Svishevs’kyi ◽  
...  
Keyword(s):  

2008 ◽  
Vol 128 (10) ◽  
pp. 615-618 ◽  
Author(s):  
Takeshi Kitajima ◽  
Akihiro Kubota ◽  
Toshiki Nakano

2019 ◽  
Author(s):  
Alexander Giovannitti ◽  
Reem B. Rashid ◽  
Quentin Thiburce ◽  
Bryan D. Paulsen ◽  
Camila Cendra ◽  
...  

<p>Avoiding faradaic side reactions during the operation of electrochemical devices is important to enhance the device stability, to achieve low power consumption, and to prevent the formation of reactive side‑products. This is particularly important for bioelectronic devices which are designed to operate in biological systems. While redox‑active materials based on conducting and semiconducting polymers represent an exciting class of materials for bioelectronic devices, they are susceptible to electrochemical side‑reactions with molecular oxygen during device operation. We show that this electrochemical side reaction yields hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>), a reactive side‑product, which may be harmful to the local biological environment and may also accelerate device degradation. We report a design strategy for the development of redox-active organic semiconductors based on donor-acceptor copolymers that prevent the formation of H<sub>2</sub>O<sub>2</sub> during device operation. This study elucidates the previously overlooked side-reactions between redox-active conjugated polymers and molecular oxygen in electrochemical devices for bioelectronics, which is critical for the operation of electrolyte‑gated devices in application-relevant environments.</p>


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