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Remote Oxidative Activation of a [Cp*Rh] Monohydride

Boyd, Emily A. and Hopkins Leseberg, Julie A. and Cosner, Emma L. and Lionetti, Davide and Henke, Wade C. and Day, Victor W. and Blakemore, James D. (2022) Remote Oxidative Activation of a [Cp*Rh] Monohydride. Chemistry - A European Journal, 28 (13). Art. No. e202104389. ISSN 0947-6539. PMCID PMC8891045. doi:10.1002/chem.202104389. https://resolver.caltech.edu/CaltechAUTHORS:20211209-231160000

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Abstract

Half-sandwich rhodium monohydrides are often proposed as intermediates in catalysis, but little is known regarding the redox-induced reactivity accessible to these species. Herein, the bis(diphenylphosphino)ferrocene (dppf) ligand has been used to explore the reactivity that can be induced when a [Cp*Rh] monohydride undergoes remote (dppf-centered) oxidation by 1e⁻. Chemical and electrochemical studies show that one-electron redox chemistry is accessible to Cp*Rh(dppf), including a unique quasi-reversible Rh^(II/I) process at −0.96 V vs. ferrocenium/ferrocene (Fc^(+/0)). This redox manifold was confirmed by isolation of an uncommon Rh^(II) species, [Cp*Rh(dppf)]⁺, that was characterized by electron paramagnetic resonance (EPR) spectroscopy. Protonation of Cp*Rh(dppf) with anilinium triflate yielded an isolable and inert monohydride, [Cp*Rh(dppf)H]+, and this species was found to undergo a quasireversible electrochemical oxidation at +0.41 V vs. Fc^(+/0) that corresponds to iron-centered oxidation in the dppf backbone. Thermochemical analysis predicts that this dppf-centered oxidation drives a dramatic increase in acidity of the Rh−H moiety by 23 pK_a units, a reactivity pattern confirmed by in situ ¹H NMR studies. Taken together, these results show that remote oxidation can effectively induce M−H activation and suggest that ligand-centered redox activity could be an attractive feature for the design of new systems relying on hydride intermediates.


Item Type:Article
Related URLs:
URLURL TypeDescription
https://doi.org/10.1002/chem.202104389DOIArticle
https://doi.org/10.26434/chemrxiv-2021-jv2ccDOIDiscussion Paper
ORCID:
AuthorORCID
Hopkins Leseberg, Julie A.0000-0001-6895-7333
Lionetti, Davide0000-0002-4937-886X
Henke, Wade C.0000-0002-4574-8544
Blakemore, James D.0000-0003-4172-7460
Additional Information:© 2022 Wiley-VCH GmbH. Issue Online: 01 March 2022; Version of Record online: 03 February 2022; Accepted manuscript online: 17 January 2022; Manuscript received: 08 December 2021. The authors thank Dr. Justin Douglas and Sarah Neuenswander for assistance with NMR and EPR spectroscopy. This work was supported by the US National Science Foundation through award OIA-1833087. Support for NMR and EPR instrumentation was provided by the US National Institutes of Health (S10OD016360 and S10RR024664) and by the US National Science Foundation (CHE-1625923). The authors declare no conflict of interest. Data Availability Statement: The data that support the findings of this study are available in the supplementary material of this article.
Funders:
Funding AgencyGrant Number
NSFOIA-1833087
NIHS10OD016360
NIHS10RR024664
CHE-1625923CHE-1625923
Subject Keywords:crystallography; electrochemistry; hydrides; ligands; redox chemistry
Issue or Number:13
PubMed Central ID:PMC8891045
DOI:10.1002/chem.202104389
Record Number:CaltechAUTHORS:20211209-231160000
Persistent URL:https://resolver.caltech.edu/CaltechAUTHORS:20211209-231160000
Official Citation:Remote Oxidative Activation of a [Cp*Rh] Monohydride. E. A. Boyd, J. A. Hopkins Leseberg, E. L. Cosner, D. Lionetti, W. C. Henke, V. W. Day, J. D. Blakemore, Chem. Eur. J. 2022, 28, e202104389.
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:112350
Collection:CaltechAUTHORS
Deposited By: George Porter
Deposited On:10 Dec 2021 20:27
Last Modified:06 May 2022 16:22

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