Insight into the isoelectronic character of azomethines and vinylenes using representative models: A spectroscopic and electrochemical study

A Bolduc, A Al Ouahabi, C Mallet…

Index: Bolduc, Andreanne; Al Ouahabi, Abelaziz; Mallet, Charlotte; Skene Journal of Organic Chemistry, 2013 , vol. 78, # 18 p. 9258 - 9269

Full Text: HTML

Citation Number: 17

Abstract

A series of azomethine and vinylene dyad and triad analogues were prepared. Their absorbance, fluorescence, and redox properties were examined experimentally and theoretically using density functional theory (DFT) calculations. These measurements were done to determine the effect of the heteroatom of the azomethine relative to its all-carbon counterpart and to assess the isoelectronic character of the two bonds. The orientation of ...

Related Articles:

One-Pot Esterification and Amide Formation via Acid-Catalyzed Dehydration and Ritter Reactions

[Dawar, Pankaj; Raju, M. Bagavan; Ramakrishna, Ramesha Andagar Synthetic Communications, 2014 , vol. 44, # 6 p. 836 - 846]

Borontrifluoride etherate promoted one-pot conversion of nitriles to esters

[Synthetic Communications, , vol. 33, # 19 p. 3461 - 3466]

A convenient procedure for esterification of carboxylic acids

[Bulletin of the Chemical Society of Japan, , vol. 51, p. 2401 - 2404]

More Articles...