Intramolecular excited proton transfer of 1-(1-phenyl-1H-phenanthro[9,10-d]imidazol-2-yl)naphthalen-2-ol – A combined experimental and quantum chemical studies-Reference-Cited by-同舟云学术

Intramolecular excited proton transfer of 1-(1-phenyl-1H-phenanthro[9,10-d]imidazol-2-yl)naphthalen-2-ol – A combined experimental and quantum chemical studies

Published:2014-03 Issue: Volume:121 Page:551-558
ISSN:1386-1425
Container-title:Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy
language:en
Short-container-title:Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy

Author:

Jayabharathi J.,Thanikachalam V.,Ramanathan P.,Arunpandiyan A.

Publisher

Elsevier BV

Subject

Spectroscopy,Instrumentation,Atomic and Molecular Physics, and Optics,Analytical Chemistry

Reference48 articles.

1. Azobenzimidazole Compounds and Polymers for Nonlinear Optics

2. An Introduction to Hydrogen Bonding;Jeffrey,1997

3. THE NATURE OF THE CHEMICAL BOND. APPLICATION OF RESULTS OBTAINED FROM THE QUANTUM MECHANICS AND FROM A THEORY OF PARAMAGNETIC SUSCEPTIBILITY TO THE STRUCTURE OF MOLECULES

4. The Weak Hydrogen Bond in Structural Chemistry and Biology;Desiraju,1999

5. Physicochemical studies of chemosensor imidazole derivatives: DFT based ESIPT process

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