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G.W. Cowell, J.N. Pitts, Jr., “Photochemical studies in rigid matrixes. II. A study of the photochemical reactivity of anthracene in polystyrene and the development of an o-nitrobenzaldehyde actinometer in poly(methyl methacrylate),” Journal of the American Chemical Society, Vol. 90, No. 5, 1968, pp. 1106-1110.

has been cited by the following article:

• TITLE: EPR Study of the Thermal Decomposition of Transannular Peroxide of Anthracene

  AUTHORS: Lubomír Lapčík, Barbora Lapčíková, Andrej Staško

  KEYWORDS: Endoperoxide, Anthracene, Free Radicals, EPR, Decomposition, Kinetics

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.1 No.2, June 30, 2011

  ABSTRACT: Thermal decomposition of transannular peroxide of anthracene (POA) (or 9,10-epidioxido anthracene) was studied by means of electron paramagnetic resonance spectroscopy (EPR) in the solid as well as in the liquid phases. Decomposition process proceeds via cleavage of the O-O bridge of the POA molecule, generating thus an alcoxy intermediate radical. Its concentration increases to a certain equilibrium stage during the time scale of the experiment. EPR spectra in the solid state were of the singlet type at the temperatures over 350 K, a doublet like anisotropic spectra were measured at the room temperature, both having g-value 2.0033. EPR spectrum from POA decomposed in benzene indicates four protons with higher (2aH = 0.305 mT, 2aH = 0.335 mT) and four protons with a lower (2aH = 0.075 mT, 2aH = 0.105 mT) splitting constants, corresponding well the radical expected after cleavage of O-O bridge.