Angupillai Satheshkumar, Kuppanagounder P Elango
Index: Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 98 , 378-83, (2012)
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Various spectroscopy techniques (UV-Vis, DRS, FT-IR, (1)H NMR, LC-MS) and theoretical computations have been employed to investigate the mechanism of the nucleophilic substitution reaction of 2,3-dichloronaphthoquinone (DCNQ) with para-substituted anilines in solid state under base- and solvent-free conditions against traditional synthetic routes. The initial formations of electron donor acceptor (EDA) adduct between DCNQ and aniline was found to be the driving force for the substitution reaction to occur in solid phase.Copyright © 2012 Elsevier B.V. All rights reserved.
| Structure | Name/CAS No. | Molecular Formula | Articles |
|---|---|---|---|
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2,3-Dichlor-1,4-naphthochinone
CAS:117-80-6 |
C10H4Cl2O2 |
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