Lutao Zhang
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
Authors
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 |
Files
Acs.inorgchem.3c02255
(8.9 Mb)
PDF
Publisher Licence URL
https://creativecommons.org/licenses/by/4.0/
Downloadable Citations
About Repository@Nottingham
Administrator e-mail: discovery-access-systems@nottingham.ac.uk
This application uses the following open-source libraries:
SheetJS Community Edition
Apache License Version 2.0 (http://www.apache.org/licenses/)
PDF.js
Apache License Version 2.0 (http://www.apache.org/licenses/)
Font Awesome
SIL OFL 1.1 (http://scripts.sil.org/OFL)
MIT License (http://opensource.org/licenses/mit-license.html)
CC BY 3.0 ( http://creativecommons.org/licenses/by/3.0/)
Powered by Worktribe © 2025
Advanced Search