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The substrates used in this study were thoroughly purified, and it was confirmed by iodometric titration that no peroxide (autoxidation initiator) was present in the olefins (<1 ppm). We thus conclude that 2 was not formed via an autoxidation process in the present case.
-
The substrates used in this study were thoroughly purified, and it was confirmed by iodometric titration that no peroxide (autoxidation initiator) was present in the olefins (<1 ppm). We thus conclude that 2 was not formed via an autoxidation process in the present case.
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77955381225
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2, as expected from Scheme 2, pathway C.
-
2, as expected from Scheme 2, pathway C.
-
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25
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37649000653
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-1), such as xanthene, 9,10-dihydroanthracene, and 1,4-cyclohexadiene. However, 2 disappeared after it was formed because it reacted with the substrates. See
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0023996141
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For KIE values in C-H bond activation by iron(III)- and copper(II)-superoxo species in iron- and copper-containing enzymes, see
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77955400881
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† were calculated (see Figures S2 and S3).?
-
† were calculated (see Figures S2 and S3).
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29
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61349161115
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2, affording cycloxadiene as a major product. An iron(IV)-oxo complex was proposed as an active oxidant for the dehydrogenation reaction. See
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2, affording cycloxadiene as a major product. An iron(IV)-oxo complex was proposed as an active oxidant for the dehydrogenation reaction. See: Mukherjee, A., Martinho, M., Bominaar, E. L., Münck, E., and Que, L., Jr. Angew. Chem., Int. Ed. 2009, 48, 1780-1783
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77955410965
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2 atmosphere using various spectroscopic methods, including EPR spectroscopy.
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2 atmosphere using various spectroscopic methods, including EPR spectroscopy.
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31
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77951685236
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III-superoxo complex is capable of abstracting a H atom from alkylaromatic compounds. See
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77955365504
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3CN (see ref 10).
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