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Title: Reactions of iron atoms with benzene and cyclohexadienes in argon matrices: iron-benzene complexes and photolytic dehydrogenation of cyclohexadiene

Journal Article · · J. Am. Chem. Soc.; (United States)
DOI:https://doi.org/10.1021/ja00281a028· OSTI ID:7222411

Three cyclic C/sub 6/ hydrocarbons-benzene (C/sub 6/H/sub 6/), 1,4-cyclohexadiene, and 1,3-cyclohexadiene (both C/sub 6/H/sub 8/)-were codeposited with iron atoms in argon matrices at 12-14 K.When iron atoms were cocondensed with benzene, infrared spectra showed the formation of Fe(C/sub 6/H/sub 6/), Fe(C/sub 6/H/sub 6/)/sub 2/, and Fe/sub 2/(C/sub 6/H/sub 6/) complexes. When iron atoms were codeposited with 1,4-cyclohexadiene, IR spectra showed the formation of Fe(C/sub 6/H/sub 8/) and Fe/sub 2/(C/sub 6/H/sub 8/) adducts. On photolysis with ultraviolet light the monoiron adduct rearranged to form FeH/sub 2/ and benzene in either isolated or adducted states. A similar dehydrogenation reaction was also thought to be observed upon photolysis of the diiron-cyclohexadiene adduct with visible light. 1,3-cyclohexadiene has been shown to react with iron atoms and dimers in a similar manner. Deuterium isotopic substitution of the three C/sub 6/ hydrocarbons was used to obtain confirmatory evidence.

Research Organization:
Rice Univ., Houston, TX
OSTI ID:
7222411
Journal Information:
J. Am. Chem. Soc.; (United States), Vol. 108:21
Country of Publication:
United States
Language:
English

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