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Published April 18, 2017 | Accepted Version + Supplemental Material
Journal Article Open

Accelerated Oxygen Atom Transfer and C−H Bond Oxygenation by Remote Redox Changes in Fe_3Mn-Iodosobenzene Adducts

Abstract

We report the synthesis, characterization, and reactivity of [Lfe_3(PhPz)_3OMn(^sPhIO)][OTf]_x (3: x=2; 4: x=3), where 4 is one of very few examples of iodosobenzene–metal adducts characterized by X-ray crystallography. Access to these rare heterometallic clusters enabled differentiation of the metal centers involved in oxygen atom transfer (Mn) or redox modulation (Fe). Specifically, ^(57)Fe Mössbauer and X-ray absorption spectroscopy provided unique insights into how changes in oxidation state (Fe^(III)_2Fe^(II)Mn^(II) vs. Fe^(III)_3Mn^(II)) influence oxygen atom transfer in tetranuclear Fe_3Mn clusters. In particular, a one-electron redox change at a distal metal site leads to a change in oxygen atom transfer reactivity by ca. two orders of magnitude.

Additional Information

© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. Version of record online: 24 March 2017; Manuscript Received: 6 February 2017. This research was supported by the NIH (R01-GM102687B). T.A. is grateful for Dreyfus and Cottrell fellowships. K.M.C is grateful for a Summer Undergraduate Research Fellowship. We thank Lawrence M. Henling for assistance with X-ray crystallography. Part of this research (XAS data collection) was carried out on beamline 7-3 at the SSRL, operated by Stanford University for the US DOE Office of Science, and supported by the DOE and NIH. XAS studies were performed with support of the Office of Science, OBES, Division of Chemical Sciences, Geosciences, and Biosciences (CSGB) of the DOE under contract no. DE-AC02-05CH11231 (J.Y.).

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Accepted Version - nihms868555.pdf

Supplemental Material - ange201701319-sup-0001-misc_information.pdf

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