Synthesis, Structural Characterisation and Solution Behaviour of High-Symmetry Lanthanide Triflate Complexes with the Sterically Demanding Phosphine Oxides Cy3PO andtBu3PO

Coles, Simon J., Pitak, Mateusz B. and PLATT, Andy (2017) Synthesis, Structural Characterisation and Solution Behaviour of High-Symmetry Lanthanide Triflate Complexes with the Sterically Demanding Phosphine Oxides Cy3PO andtBu3PO. European Journal of Inorganic Chemistry, 2017 (11). pp. 1464-1471. ISSN 1434-1948

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Abstract or description

The synthesis and characterisation of complexes formed from lanthanide trifluoromethanesulfonates [Ln(OTf)3] and tricyclohexylphosphine oxide (Cy3PO) or tri‐tert‐butylphosphine oxide (tBu3PO) are described. The structures of [Ln(H2O)5(Cy3PO)2]·2R3PO·(OTf)3 (Ln = Pr, Tm; R = Cy and Ln = Nd; R = tBu) are pentagonal bipyramidal with an equatorial plane of five H2O ligands and two axial Cy3PO ligands. The remaining Cy3PO molecules are H‐bonded to the coordinated water molecules, as are the triflate anions. NMR spectroscopy showed that the triflate ions remain associated with the complexes in CDCl3 solution. Lanthanide‐induced shifts in the 19F and 31P NMR spectra confirm that one structure is present for all the lanthanides with an additional structure for the heavier metals. The acidity of the complexes was examined by 31P NMR spectroscopic studies on the reactions between [Ln(H2O)5(Cy3PO)2]·2Cy3PO·(OTf)3 (Ln = La, Eu, Er, Lu) and phosphines PR3 (R = Ph, mesityl, Cy), Ph2PC2H4PPh2 and Ph2PC3H6PPh2. Protonation of the more basic phosphines and H‐bonding to the less basic phosphines is observed.

Item Type:	Article
Additional Information:	** From Crossref via Jisc Publications Router. ** Licence for VoR version of this article starting on 21-03-2017: http://onlinelibrary.wiley.com/termsAndConditions
Uncontrolled Keywords:	Inorganic Chemistry
Faculty:	School of Law, Policing and Forensics > Law
SWORD Depositor:	JISC pubrouter
Depositing User:	JISC pubrouter
Date Deposited:	20 Aug 2018 12:30
Last Modified:	24 Feb 2023 13:52
Related URLs:	Publisher
URI:	https://eprints.staffs.ac.uk/id/eprint/4671

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