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Phosphine and Selenoether peri-Substituted Acenaphthenes and Their Transition-Metal Complexes: Structural and NMR Investigations

Zhang, Lutao; Christie, Francesca A.; Tarcza, Anna E.; Lancaster, Helena G.; Taylor, Laurence J.; Bühl, Michael; Malkina, Olga L.; Woollins, J. Derek; Carpenter-Warren, Cameron L.; Cordes, David B.; Slawin, Alexandra M.Z.; Chalmers, Brian A.; Kilian, Petr

Phosphine and Selenoether peri-Substituted Acenaphthenes and Their Transition-Metal Complexes: Structural and NMR Investigations Thumbnail


Authors

Lutao Zhang

Francesca A. Christie

Anna E. Tarcza

Helena G. Lancaster

Laurence J. Taylor

Michael Bühl

Olga L. Malkina

J. Derek Woollins

Cameron L. Carpenter-Warren

David B. Cordes

Alexandra M.Z. Slawin

Brian A. Chalmers

Petr Kilian



Abstract

A series of -substituted acenaphthene-based phosphine selenoether bidentate ligands Acenap( Pr P)(SeAr) ( - , Acenap = acenaphthene-5,6-diyl, Ar = Ph, mesityl, 2,4,6-trisopropylphenyl and supermesityl) were prepared. The rigid acenaphthene framework induces a forced overlap of the phosphine and selenoether lone pairs, resulting in a large magnitude of through-space coupling, ranging from 452 to 545 Hz. These rigid ligands - were used to prepare a series of selected late d-block metals, mercury, and borane complexes, which were characterized, including by multinuclear NMR and single-crystal X-ray diffraction. The Lewis acidic motifs (BH , Mo(CO) , Ag , PdCl , PtCl , and HgCl ) bridge the two donor atoms (P and Se) in all but one case in the solid-state structures. Where the bridging motif contained NMR-active nuclei ( B, Ag, Ag, Pt, and Hg), and couplings are observed directly, in addition to the altered in the respective NMR spectra. The solution NMR data are correlated with single-crystal diffraction data, and in the case of mercury(II) complexes, they are also correlated with the solid-state NMR data and coupling deformation density calculations. The latter indicate that the through-space interaction dominates in free , while in the complex, the main coupling pathway is via the metal atom and not through the carbon framework of the acenaphthene ring system.

Citation

Zhang, L., Christie, F. A., Tarcza, A. E., Lancaster, H. G., Taylor, L. J., Bühl, M., Malkina, O. L., Woollins, J. D., Carpenter-Warren, C. L., Cordes, D. B., Slawin, A. M., Chalmers, B. A., & Kilian, P. (2023). Phosphine and Selenoether peri-Substituted Acenaphthenes and Their Transition-Metal Complexes: Structural and NMR Investigations. Inorganic Chemistry, 62(39), 16084–16100. https://doi.org/10.1021/acs.inorgchem.3c02255

Journal Article Type Article
Acceptance Date Sep 18, 2023
Online Publication Date Sep 18, 2023
Publication Date Oct 2, 2023
Deposit Date Sep 29, 2023
Publicly Available Date Oct 13, 2023
Journal Inorganic Chemistry
Print ISSN 0020-1669
Electronic ISSN 1520-510X
Publisher American Chemical Society
Peer Reviewed Peer Reviewed
Volume 62
Issue 39
Pages 16084–16100
DOI https://doi.org/10.1021/acs.inorgchem.3c02255
Keywords Group 15 compounds, Ligands, Mercury, Metals, Nuclear magnetic resonance spectroscopy
Public URL https://nottingham-repository.worktribe.com/output/25391175
Publisher URL https://pubs.acs.org/doi/10.1021/acs.inorgchem.3c02255

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