Rate the Article: Computational Study of C-Substituted Tetrazole Tautomers: Magnetic and Structural Based Degree of Aromaticity, IJSR, Call for Papers, Online Journal
International Journal of Science and Research (IJSR)

International Journal of Science and Research (IJSR)
Call for Papers | Fully Refereed | Open Access | Double Blind Peer Reviewed

ISSN: 2319-7064

Downloads: 110 | Views: 315

Research Paper | Chemistry | India | Volume 4 Issue 3, March 2015 | Rating: 6.6 / 10


Computational Study of C-Substituted Tetrazole Tautomers: Magnetic and Structural Based Degree of Aromaticity

Joseph Lalhruaitluanga, Zodinpuia Pachuau


Abstract: This study focused on the influence of substitution on the degree of aromaticity of tetrazole tautomers. All the structures were fully optimised at the DFT B3lyp (three parameter hybrid functional of Becke using Lee-Yang-Parr correlation function) method incorporating various basis sets. Interesting results were obtained regarding aromatic properties for the 1H- and 2H-Tetrazole isomers substituted with the selected substituents. Magnetic and Geometry based degree of aromaticity show strong aromatic character.


Keywords: Tetrazole, Aromaticity, DFT, NICS, Bird index


Edition: Volume 4 Issue 3, March 2015,


Pages: 1165 - 1168



Rate this Article


Select Rating (Lowest: 1, Highest: 10)

5

Your Comments (Only high quality comments will be accepted.)

Characters: 0

Your Full Name:


Your Valid Email Address:


Verification Code will appear in 2 Seconds ... Wait

Top