Quantum-chemical study of N,N´-diphenyl-p-phenylenediamine (DPPD) dehydrogenation
Anton Gatial *, Júlia Polovková a, Martin Breza
Institute of Physical Chemistry and Chemical Physics, Slovak University of Technology,
SK-81237 Bratislava, Slovakia
a Institute of Measurement Science, Slovak Academy of Sciences, SK-84104 Bratislava, Slovakia
E-mail: * anton.gatial@stuba.sk
Abstract: Using B3LYP/6-31G* treatment, the optimal geometries and IR spectra of N,N´-diphenyl-p-phenylenediamine antioxidant (DPPD) and of N,N´-diphenyl-p-quinonediimine (DQDI) as its double dehydrogenated oxidation product have been obtained. The complete conformation analysis predicts the existence of four stable conformers of each of the systems under study. Experimental IR spectra of DPPD sample heated on air at 140 ºC confirmed the DQDI formation even at increased temperatures.
Keywords: Antioxidants; N,N´-substituted p-phenylenediamines; dehydrogenated structures; IR spectra; DFT geometry optimization
Full paper in Portable Document Format: acs_0007.pdf
Acta Chimica Slovaca, Vol. 1, No. 1, 2008, pp. 72—84