A RATIONAL SYNTHESIS OF A NOVEL IMIDAZO[4,5-f][1,10] PHENANTHROLINE TEMPLATED SCHIFF BASE: CHARACTERIZATION, PHOTOLUMINESCENCE AND DFT/TD-DFT STUDY


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Karslioglu S., Demir S., Yilmaz H., Gorduk S.

BULLETIN OF THE CHEMICAL SOCIETY OF ETHIOPIA, vol.31, no.1, pp.137-147, 2017 (Peer-Reviewed Journal) identifier identifier

  • Publication Type: Article / Article
  • Volume: 31 Issue: 1
  • Publication Date: 2017
  • Doi Number: 10.4314/bcse.v31i1.12
  • Journal Name: BULLETIN OF THE CHEMICAL SOCIETY OF ETHIOPIA
  • Journal Indexes: Science Citation Index Expanded, Scopus
  • Page Numbers: pp.137-147

Abstract

A new imidazo[4,5-f][1,10] phenanthroline (imp) derivative imidazo-N-5, N-6-bis((4-(1Himidazo[ 4,5-f][1,10] phenanthroline-2-yl) phenyl) methylene)-1,10-phenanthroline-5,6-diamine (impap) was synthesized in five steps starting from bare phenanthroline (phen) precursors. The novel compound was fully characterized by H-1-NMR, IR, elemental analysis and electrospray ionization mass spectroscopy (ESI-MS) techniques. Solid state emission spectrum of impap showed two distinct strong emission maxima with large Stokes shifts. The ground state gas phase geometry of impap was predicted by DFT calculations. Excited state properties of the molecule were examined through TD-DFT calculations conducted at the optimized geometry. Responsible transitions for the strong fluorescence of impap were assigned to single component charge transfer transitions with large oscillator strengths based on the ground state calculated molecular orbital contributions.