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  • Electronic, infrared, and 1HNMR spectral studies of the novel charge-transfer complexes of o-tolidine and p-toluidine with alternation π-acceptors (3,5-dinitro benzoic acid and 2,6-Dichloroquinone-4-chloroimide (cas 101-38-2)) in CHCl3 solvent
  • Add time:08/03/2019         Source:sciencedirect.com

    The rapid interaction between o-tolidine and p-toluidine (π-donors) with the π-acceptors, e.g., 3,5-dinitrobenzoic acid (DNB) and 2,6-dichloroquinone-4-chloroimide (DCQ) results in the formation of 1:1 charge-transfer complexes as the final products, [(o-tolidine) (acceptor)] and [(p-toluidine) (acceptor)]. The final products of the reactions have been isolated and characterized using FTIR, 1HNMR spectroscopy and elemental analysis as well as photometric titration. The stoichiometry and apparent formation constants of the complexes formed were determined by applying the conventional spectrophotometric molar ratio method.

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    Prev:Biochemical and structural characterization of recombinant hyoscyamine 6β-hydroxylase from Datura metel L.
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