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Kameda, T., Inazu, K., Asano, K., Murota, M., Takenaka, N., Sadanaga, Y., Hisamatsu, Y. and Bandow, H. (2013) Prediction of Rate Constants for the Gas Phase Reactions of Triphenylene with OH and NO3 Radicals Using a Relative Rate Method in CCl4 Liquid Phase-System. Chemosphere, 90, 766-771.
https://doi.org/10.1016/j.chemosphere.2012.09.071

has been cited by the following article:

• TITLE: A Theoretical Investigation of Gas Phase OH-Initiated Acenaphthylene Degradation Reaction

  AUTHORS: Xin Mao, Sufan Wang, Yucheng Huang, Tao Zhou

  KEYWORDS: Polycyclic Aromatic Hydrocarbons, Acenaphthylene, Gas Phase, Nitroacenaphthylene, Degradation

  JOURNAL NAME: Computational Chemistry, Vol.5 No.1, January 6, 2017

  ABSTRACT: The mechanisms for OH-initiated acenaphthylene degradation reactions are investigated theoretically by using the density function theory method at M06-2X/aug-cc-pVTZ level in the present paper. There are two possible reaction pathways for the degradation processes have been predicted: the hydrogen abstraction pathway and the hydroxyl addition elimination pathway. Additionally, the formation mechanism for a series of the products such as epoxide, naphthalene-1,8-dicarbaldehyde, dialdehydes, 1-acenaphthenone and nitroacenaphthylene are discussed in detail as well. From the analyses of the decomposition of OH-acenaphthylene adducts, it is found that the favorable reaction with O2/NO is to form the acenaphthenone rather than epoxide, and the most stable isomer is acenaphthenone react from the C1-site reaction. The advantage reaction pathway with NO2 is to form nitroacenaphthylene and nitroacenaphthylenol from C1-site, too.