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Products, radical intermediates, and hydrogen atom production in the thermal decomposition of 1,2-dihydronaphthalene

Journal Article · · J. Am. Chem. Soc.; (United States)
DOI:https://doi.org/10.1021/jo00193a022· OSTI ID:6313623

The thermal decomposition of 1,2-dihydronaphthalene (DHN) at 300/sup 0/ produces tetralin, naphthalene, hydrogen, and five C/sub 20/ hydrocarbon products. The isolation of five C/sub 20/ hydrocarbon compounds revealed that two of the compounds are formed by the addition of 2-hydronaphthyl to DHN followed by intramolecular cyclization and hydrogen abstraction. A third compound was formed by the addition of the 1-tetralyl radical to DHN followed by hydrogen abstraction, and the other two compounds were formed by a sequence involving initial addition of 2-tetralyl radical to DHN. The thermal decomposition of DHN at 400-450/sup 0/C leads to the formation of a hydrogen atom which participates in subsequent hydrocracking reactions of available substituted aromatic structures.

Research Organization:
Pacific Northwest Lab., Richland, WA
DOE Contract Number:
AC06-76RL01830; AC02-79ER10510
OSTI ID:
6313623
Journal Information:
J. Am. Chem. Soc.; (United States), Journal Name: J. Am. Chem. Soc.; (United States) Vol. 106:20; ISSN JACSA
Country of Publication:
United States
Language:
English