Mahdieh Entezari
Department of Chemistry, Islamic azad university, mahshahr branch, Mahshahr, Iran
[ 1 ] - Internal strain on the bond length and rate of hydrolysis in cyclic amides
The internal strain in cyclic amides are explained as a factor of resonance that are effected on the bond length C-N and are a major factor of rates of hydrolysis. The cyclic amides in this study are optimized by Gaussian program and the bond length of C-N in the rings are studied by HF/6-31G*.
[ 2 ] - conformational properties and the anomeric effect study of phosphinanes
Ab initio HF/6-31G* Methode was employed to calculate the bond length in 2- phosphinanes when electronegative groups was at C-2 tend axial and equatorial positions. The magnitude of the anomeric effect depends on the nature of the substituent, the effect of the substituent can be seen by comparing the bond length in 2-chloro and 2- boromo substituented phosphinanes. The effect of anomeric effec...
[ 3 ] - Synthesis and Application of Heterocyclic as ultraviolet Absorbers
The lifespan of organic coatings is reduced in outdoor applications by attacks of solar radiation, oxygen and atmospheric pollutants. Degradation of coating and recoating introduce pollutants into the environment. For solvent base coatings like alkyd paints volatile organic compounds (VOC) are main source of pollution. Undesirable mechanical, physical and chemical consequences of the resulting ...
[ 4 ] - Theoretical study of the effect of internal strain on the bond length and rate of hydrolysis in cyclic amides
The internal strain in cyclic amides are explained as a factor of resonance that are effected on the bond length C-N and are a major factor of rates of hydrolysis. The cyclic amides in this study are optimized by Gaussian program and the bond length of C-N in the rings are studied by HF/6-31G*.
[ 5 ] - Theoretical study of conformational properties and the anomeric effect study of the 2- phosphinanes
Ab initio HF/6-31G* Methode was employed to calculate the bond length in 2- phosphinanes when electronegative groups was at C-2 tend axial and equatorial positions. The magnitude of the anomeric effect depends on the nature of the substituent, the effect of the substituent can be seen by comparing the bond length in 2-chloro and 2-boromo substituented phosphinanes. The effect of anomeric eff...
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