Theoretical study of conformational properties and the anomeric effect study of the 2- phosphinanes

Document Type : Original Paper

Authors

1 Department of chemistry, Science and Reaserch branch, Islamic azad university, Tehran, Iran, Corresponding author E-mail address: j-azizian@cc.sbu.ac.ir

2 bDepartment of chemistry, , Mahshahr branch, Islamic azad university, Mahshahr, Iran

3 Department of chemistry, , Mahshahr branch, Islamic azad university, Mahshahr, Iran

Abstract

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. 

Keywords

International Journal of Heterocyclic Chemistry
Volume 8, Issue 2
Spring 2018
Pages 55-61

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