conformational properties and the anomeric effect study of phosphinanes
الموضوعات : International Journal of Heterocyclic Chemistry
Javad Azizian
1
(Department of chemistry, Science and Reaserch branch, Islamic azad
university, Tehran, Iran)
Mahdieh Entezari
2
(Department of chemist r,y Mahshahr branch, Islamic azad university,
Mahshahr, Iran)
Hossein Anaraki Ardakani
3
(Department of chemist r,y Mahshahr branch, Islamic azad university,
Mahshahr, Iran)
Shahab Zomorodbakhsh
4
(Department of chemist r,y Mahshahr branch, Islamic azad university,
Mahshahr, Iran)
الکلمات المفتاحية: bond length, anomeric effect, 2- phosphinane, axial and equatorial position, Ab initio calculations,
ملخص المقالة :
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 effect have been effected on the bond length in 2-phosphinanes.
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