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|a Stubbs, Amanda Walcott
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|a Massachusetts Institute of Technology. Department of Chemistry
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|a Dinca, Mircea
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|a Selective oxidation of C-H bonds through a manganese(III) hydroperoxo in MnII-exchanged CFA-1
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|a Selective oxidation of C-H bonds through a manganese(III) hydroperoxo in Mn[superscript II]-exchanged CFA-1
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|b American Chemical Society (ACS),
|c 2020-07-17T18:48:20Z.
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|z Get fulltext
|u https://hdl.handle.net/1721.1/126240
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|a Partial substitution of Zn[superscript II] by Mn[superscript II] in Zn[subscript 5](OAc)[subscript 4](5,5'-bibenzo[d][1,2,3]triazole)[subscript 3] (CFA-1) results in a Mn[superscript II] species supported by three nitrogen ligands and a charge-balancing anion, a structure reminiscent of those found in molecular "scorpionate" complexes. Unlike molecular manganese(II) scorpionates, Mn-CFA-1 is capable of catalytically activating oxygen from air to oxidize C-H bonds up to 87 kcal/mol in strength. A series of in situ spectroscopic studies, including diffuse-reflectance UV-vis, diffuse-reflectance infrared Fourier transform spectroscopy, and X-ray absorption spectroscopy, reveal that catalysis likely proceeds through a manganese(III) hydroperoxo that is only accessed in the presence of a hydrogen-atom donor. These results demonstrate that the site isolation provided in metal-organic frameworks enables the generation and utilization of highly reactive species for catalysis that are inaccessible in molecular systems.
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|a National Science Foundation (Award DMR1452612)
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|a National Science Foundation (Grant 1122374)
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|a Article
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|t 10.1021/acs.inorgchem.9b02068
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|t Inorganic Chemistry
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