ChemInform Abstract: Highly Regio- and Stereoselective Synthesis of Allylsilanes via Palladium-Catalyzed Reductive Metalation of Allylic Phosphates with a SmI2-HMPA System. Stereochemical Aspect of the Tandem Electron Transfer Process in Allylic Systems.

ChemInform ◽  
2010 ◽  
Vol 28 (47) ◽  
pp. no-no
Author(s):  
T. HANAMOTO ◽  
A. SUGINO ◽  
T. KIKUKAWA ◽  
J. INANAGA
Keyword(s):  
Electron Transfer ◽  
Transfer Process ◽  
Stereoselective Synthesis ◽  
Electron Transfer Process ◽  
Palladium Catalyzed ◽  
Stereochemical Aspect

Visible-light-induced phenylchalcogenyl-oxygenation of allenes having aryl or electron withdrawing substituents with ambient air as a sole oxidant

2016 ◽  
Vol 14 (48) ◽  
pp. 11415-11425 ◽  
Author(s):  
Gullapalli Kumaraswamy ◽  
Swargam Vijaykumar ◽  
Kukkadapu Ankamma ◽  
Vykunthapu Narayanarao
Keyword(s):  
Electron Transfer ◽  
Visible Light ◽  
Transfer Process ◽  
Stereoselective Synthesis ◽  
Ambient Air ◽  
Single Electron ◽  
Single Electron Transfer ◽  
Electron Transfer Process ◽  
Electron Withdrawing Substituents

The stereoselective synthesis of α-phenylselenyl- or telluryl β-aryl acrylaldehydes/ketones from aryl allenes/1,3-diarylallene by an oxidative photo-induced single electron transfer process using benign ambient air as a sole oxidant was achieved.

Thionine–graphene oxide covalent hybrid and its interaction with light

2017 ◽  
Vol 19 (22) ◽  
pp. 14412-14423 ◽  
Author(s):  
Ewelina Krzyszkowska ◽  
Justyna Walkowiak-Kulikowska ◽  
Sven Stienen ◽  
Aleksandra Wojcik
Keyword(s):  
Electron Transfer ◽  
Graphene Oxide ◽  
Excited State ◽  
Transfer Process ◽  
Singlet Excited State ◽  
Functionalized Graphene ◽  
Electron Transfer Process ◽  
Functionalized Graphene Oxide ◽  
Back Electron Transfer

Quenching of the thionine singlet excited state in covalently functionalized graphene oxide with an efficient back electron transfer process.

scholarly journals Electrokinetic and Impedimetric Dynamics of FeCo-Nanoparticles on Glassy Carbon Electrode

Nano Hybrids ◽  
2013 ◽  
Vol 3 ◽  
pp. 1-23 ◽  
Author(s):  
Chinwe O. Ikpo ◽  
Njagi Njomo ◽  
Kenneth I. Ozoemena ◽  
Tesfaye Waryo ◽  
Rasaq A. Olowu ◽  
...  
Keyword(s):  
Electron Transfer ◽  
Glassy Carbon Electrode ◽  
Glassy Carbon ◽  
Transfer Process ◽  
Dimethyl Carbonate ◽  
Electrochemical Impedance ◽  
Ethylene Carbonate ◽  
Carbon Electrode ◽  
Electron Transfer Process ◽  
Feco Nanoparticles

The electrochemical dynamics of a film of FeCo nanoparticles were studied on a glassy carbon electrode (GCE). The film was found to be electroactive in 1 M LiClO4 containing 1:1 v/v ethylene carbonate dimethyl carbonate electrolyte system. Cyclic voltammetric experiments revealed a diffusion-controlled electron transfer process on the GCE/FeCo electrode surface. Further interrogation on the electrochemical properties of the FeCo nanoelectrode in an oxygen saturated 1 M LiClO4 containing 1:1 v/v ethylene-carbonate-dimethyl carbonate revealed that the nanoelectrode showed good response towards the electro-catalytic reduction of molecular oxygen with a Tafel slope of about 120 mV which is close to the theoretical 118 mV for a single electron transfer process in the rate limiting step; and a transfer coefficient (α) of 0.49. The heterogeneous rate constant of electron transfer (ket), exchange current density (io) and time constant (τ) were calculated from data obtained from electrochemical impedance spectroscopy and found to have values of 2.3 x 10-5 cm s-1, 1.6 x 10-4 A cm-2 and 2.4 x 10-4 s rad-1, respectively.

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