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Published November 13, 2017 | Supplemental Material + Accepted Version
Journal Article Open

Terminal Molybdenum Phosphides with d Electrons: Radical Character Promotes Coupling Chemistry

Abstract

A terminal Mo phosphide was prepared via group transfer of both P- and Cl-atoms from chloro-substituted dibenzo-7λ^3-phosphanorbornadiene. This compound represents the first structurally characterized terminal transition metal phosphide with valence d electrons. In the tetragonal ligand field, these electrons populate an orbital of d_(xy) parentage, an electronic configuration that accommodates both metal d-electrons and a formal M≡P triple bond. Single electron oxidation affords a transient open shell terminal phosphide cation with significant spin density on P, as corroborated by CW and pulsed EPR characterization. Facile P-P bond formation occurs from this species via intermolecular phosphide coupling.

Additional Information

© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. Manuscript received: August 2, 2017; Accepted manuscript online: September 6, 2017; Version of record online: October 10, 2017. We thank Lawrence M. Henling and Dr. Mike Takase for crystallographic assistance, Dr. David VanderVelde for help with NMR experiments, and Dr. A. Velian and Prof. C. C. Cummins for stimulating discussions. T.A. is grateful for Sloan, Cottrell, and Dreyfus fellowships and J.A.B. for an NSF graduate research fellowship. This research was supported by the NSF, grant numbers CHE-1151918 (T.A.) and NSF-1531940 (EPR instrumentation), and Caltech.

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Accepted Version - Buss_et_al-2017-Angewandte_Chemie.pdf

Supplemental Material - anie201707921-sup-0001-SI1.pdf

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August 21, 2023
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