scholarly journals High Spin Molecules: [Mn12O12(O2CCH2Cl)16(H2O)4] and the One-electron Reduction Product [PPh4][Mn12O12(O2CCH2Cl)16(H2O)3]

2000 ◽  
Vol 29 (4) ◽  
pp. 346-347 ◽  
Author(s):  
Hui-Lien Tsai ◽  
Tyn-Yih Jwo ◽  
Gene-Hsiang Lee ◽  
Yu Wang
Keyword(s):  
High Spin ◽  
Reduction Product ◽  
Electron Reduction ◽  
The One

Identification of two reduction products of glyoxal bis(2-mercaptoanil)nickel. Characterization of the one-electron reduction product and the partially hydrogenated anion

1967 ◽  
Vol 89 (10) ◽  
pp. 2278-2281 ◽  
Author(s):  
F. Lalor ◽  
M. Frederick. Hawthorne ◽  
August H. Maki ◽  
K. Darlington ◽  
Alan. Davison ◽  
...  
Keyword(s):  
Reduction Product ◽  
Electron Reduction ◽  
The One

Theoretical insights into the reductive metabolism of CCl4 by cytochrome P450 enzymes and the CCl4-dependent suicidal inactivation of P450

2014 ◽  
Vol 43 (39) ◽  
pp. 14833-14840 ◽  
Author(s):  
Xiao-Xi Li ◽  
Qing-Chuan Zheng ◽  
Yong Wang ◽  
Hong-Xing Zhang
Keyword(s):  
Cytochrome P450 ◽  
Reduction Product ◽  
Cytochrome P450 Enzymes ◽  
Electron Reduction ◽  
The One ◽  
Reductive Metabolism

The one-electron reduction product, ˙CCl3, irreversibly inactivates P450 via covalently binding to the meso-carbon, whereas the two successive one-electron reductions product, :CCl2, reversibly inhibits P450 by coordinating to iron.

scholarly journals EPR and DFT studies of the one-electron reduction product of phospholium cations

2006 ◽  
Vol 8 (7) ◽  
pp. 862-868 ◽  
Author(s):  
Prashant Adkine ◽  
Thibault Cantat ◽  
Eliane Deschamps ◽  
Louis Ricard ◽  
Nicolas Mézailles ◽  
...  
Keyword(s):  
Reduction Product ◽  
Dft Studies ◽  
Electron Reduction ◽  
The One

The photochemistry of Ru(bpy)32+ in basic medium

1982 ◽  
Vol 60 (22) ◽  
pp. 2856-2858 ◽  
Author(s):  
Jin-Gou Xu ◽  
Gerald B. Porter
Keyword(s):  
Electron Transfer ◽  
Methyl Viologen ◽  
Reduction Product ◽  
Basic Medium ◽  
Electron Reduction ◽  
The One

Ru(bpy)32+ is photodecomposed in 0.3 M NaOH with [Formula: see text]. With methyl viologen also present, electron transfer quenching of the luminescence is accompanied by formation of the one electron reduction product of methyl viologen, MV+. The Ru(bpy)33+ formed in the corresponding oxidation is rapidly reduced by either OH− or MV+ to Ru(II).

Reactivity of the one-electron reduction product from nifedipine with relevant biological targets

1996 ◽  
Vol 101 (2) ◽  
pp. 89-101 ◽  
Author(s):  
Luis J. Núñez-Vergara ◽  
P.A. Navarrete-Encina ◽  
M.E. Ortiz ◽  
S. Bollo ◽  
J.A. Squella
Keyword(s):  
Reduction Product ◽  
Biological Targets ◽  
Electron Reduction ◽  
The One

Redox behaviour of nifuroxazide: generation of the one-electron reduction product

1996 ◽  
Vol 99 (1-3) ◽  
pp. 227-238 ◽  
Author(s):  
J.A. Squella ◽  
M.E. Letelier ◽  
L. Lindermeyer ◽  
L.J. Nuñez-Vergara
Keyword(s):  
Reduction Product ◽  
Redox Behaviour ◽  
Electron Reduction ◽  
The One
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