SYNTHESIS AND PHOTOPHYSICAL PROPERTIES OF A SCHIFF BASE DERIVED FROM PYROLE-2-ALDEHYDE AND 3,3�-DIAMINO-N-METHYL DIPROPYL AMINE

Susanta kumar Giri

Volume : IV, Issue : X, October - 2015

SYNTHESIS AND PHOTOPHYSICAL PROPERTIES OF A SCHIFF BASE DERIVED FROM PYROLE-2-ALDEHYDE AND 3,3�-DIAMINO-N-METHYL DIPROPYL AMINE

Susanta Kumar Giri

Abstract :

Schiff base ligands have been extensively studied in co-ordination chemistry, mainly due to their facile synthesis, tunable steric and electronic properties. It is well known that ligands containing �N� and �O� atoms can easily co-ordinate metal ions. Therefore Schiff base ligands possessing N,O-donor and chromophore groups are of important building blocks to construct luminescence complexes[1]. The pyrolide anions have received particular research interest, because they offer a reasonable mimic of the cyclopentadienyl functions and could act as competent η5 ligand. Additionally, the pyrolide anions afford the possibility of forming σ-bond through the ring nitrogen donor, providing tunable steric and electronic features required for compensating coordinative unsaturation of metal atoms and enhancing catalytic activity towards polymerization[2]. We have successfully synthesized one of such ligand starting from pyrole-2-aldehyde.