Structure and decomposition path of the HIF radical

1991 ◽  
Vol 95 (1) ◽  
pp. 433-440 ◽  
Author(s):  
Stanislaw A. Kucharski ◽  
Rodney J. Bartlett
Keyword(s):  
Decomposition Path

A theoretical study on the stability of the C3NN radical and its decomposition path

1981 ◽  
Vol 83 (1) ◽  
pp. 78-82 ◽  
Author(s):  
K. Yamashita ◽  
M. Kaminoyama ◽  
T. Yamabe ◽  
K. Fukui
Keyword(s):  
Theoretical Study ◽  
The Stability ◽  
Decomposition Path

Transient ordered phases with different structure types along a phase-decomposition path

1999 ◽  
Vol 59 (1) ◽  
pp. 16-19 ◽  
Author(s):  
Zhi-Rong Liu ◽  
Bing-Lin Gu ◽  
Hong Gui ◽  
Xiao-Wen Zhang
Keyword(s):  
Phase Decomposition ◽  
Ordered Phases ◽  
Decomposition Path

Adjustment of the decomposition path for Na2LiAlH6 by TiF3 addition

2011 ◽  
Vol 36 (19) ◽  
pp. 12279-12285 ◽  
Author(s):  
Jon Erling Fonneløp ◽  
Ole Martin Løvvik ◽  
Magnus H. Sørby ◽  
Hendrik W. Brinks ◽  
Bjørn C. Hauback
Keyword(s):  
Decomposition Path

Li24[MnN3]3N2and Li5[(Li1-xMnx)N]3, Two Intermediates in the Decomposition Path of Li7[MnN4] to Li2[(Li1-xMnx)N]:  An Experimental and Theoretical Study

2001 ◽  
Vol 40 (20) ◽  
pp. 5215-5222 ◽  
Author(s):  
R. Niewa ◽  
F. R. Wagner ◽  
W. Schnelle ◽  
O. Hochrein ◽  
R. Kniep
Keyword(s):  
Theoretical Study ◽  
Decomposition Path

scholarly journals Qualitative and Quantitative Reversed-Phase Liquid Chromatography of a New Bisisoxazolylnaphthoquinone

2002 ◽  
Vol 85 (2) ◽  
pp. 349-354
Author(s):  
Carola F Ferreyra ◽  
Cristina S Ortiz ◽  
María M de Bertorello
Keyword(s):  
Degradation Products ◽  
Reversed Phase ◽  
Reversed Phase Liquid Chromatography ◽  
Symmetry Factor ◽  
Phase Liquid ◽  
Internal Standardization ◽  
The Stability ◽  
Ph Range ◽  
Liquid Chromatographic ◽  
Decomposition Path

Abstract The main objective of this study was to develop and test the applicability of a sensitive, accurate, and precise liquid chromatographic (LC) method for evaluating the stability characteristics of a new bisisoxazolylnaphthoquinone, 2-(3,5-dimethyl-4-isoxazolylamino)-N-(3,5-dimethyl-4-isoxazolyl)-1,4-naphthoquinone-4-imine compound 1. The method was shown to be selective and stability-indicating. Isocratic elution with a mobile phase of methanol–water (75 + 25, v/v) on a reversed-phase column with UV detection at ambient temperature completely resolved compound 1 from its degradation products. The LC system was calibrated by plotting peak responses versus known concentrations of a reference standard by using an internal standardization procedure. Complete elution occurred after 12 min with a peak symmetry factor of 0.95 for the drug peak. The kinetic degradation of compound 1 was studied over a pH range of 0.88–14.00 to determine the kinetic parameters involved in its decomposition path in aqueous solution.

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