A Low-Valent Molybdenum Nitride Complex: Reduction Promotes Carbonylation Chemistry
Abstract
Toward nitrogen functionalization, reactive terminal transition metal nitrides with high d‐electron counts are of interest. A series of terminal Mo^(IV) nitride complexes were prepared within the context of exploring nitride/carbonyl coupling to cyanate. Reduction affords the first Mo^(II) nitrido complex, an early metal nitride with four valence d‐electrons. The binding mode of the para‐terphenyl diphosphine ancillary ligand changes to stabilize an electronic configuration with a high electron count and a formal M−N bond order of three. Even with an intact Mo≡N bond, this low‐valent nitrido complex proves to be highly reactive, readily undergoing N‐atom transfer upon addition of CO, releasing cyanate anion.
Additional Information
© 2018 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim. Manuscript received: March 28, 2018; Revised manuscript received: May 31, 2018; Accepted manuscript online: June 5, 2018; Version of record online: July 4, 2018. We thank Lawrence M. Henling and Dr. Mike Takase for crystallographic assistance, Dr. David VanderVelde for NMR expertise, and Dr. Gwendolyn A. Bailey for collecting IR and EA data. T.A. is grateful for a Dreyfus fellowships and J.A.B. for an NSF graduate research fellowship. This research was supported by the NSF, grant number CHE‐1151918 (T.A.), and Caltech. The authors declare no conflict of interest.Attached Files
Supplemental Material - anie201803728-sup-0001-si1.pdf
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Additional details
- Alternative title
- A Low-Valent Molybdenum Nitride: Reduction Promotes Carbonylation Chemistry
- Eprint ID
- 86937
- Resolver ID
- CaltechAUTHORS:20180608-143739694
- Camille and Henry Dreyfus Foundation
- NSF Graduate Research Fellowship
- NSF
- CHE-1151918
- Created
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2018-06-08Created from EPrint's datestamp field
- Updated
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2021-11-15Created from EPrint's last_modified field