Synthesis of the bulky phosphanide [P(SiiPr3)2]− and its stabilization of low-coordinate group 12 complexes

Churchill, Olivia P., Dase, Antonia, Taylor, Laurence J., Argent, Stephen P., Coles, Nathan T. ORCID: https://orcid.org/0000-0001-6190-9080, Walker, Gavin S. and Kays, Deborah L. ORCID: https://orcid.org/0000-0002-4616-6001 2024. Synthesis of the bulky phosphanide [P(SiiPr3)2]− and its stabilization of low-coordinate group 12 complexes. Inorganic Chemistry 63 (43) , pp. 20286-20294. 10.1021/acs.inorgchem.4c03134

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Abstract

Here, we report an improved synthesis of the bulky phosphanide anion [P(SiiPr3)2]− in synthetically useful yields and its complexation to group 12 metals. The ligand is obtained as the sodium salt NaP(SiiPr3)2 1 in a 42% isolated yield and a single step from red phosphorus and sodium. This is a significantly higher-yielding and safer preparation compared to the previously reported synthesis of this ligand, and we have thus applied 1 to the synthesis of the two-coordinate complexes M[P(SiiPr3)2]2 (M = Zn, Cd, Hg). These group 12 complexes are all monomeric and with nonlinear P–M–P angles in the solid state, with DFT calculations suggesting that this bending is due to the steric demands of the ligand. Multinuclear NMR spectroscopy revealed complex second-order splitting patterns due to strong PP’ coupling. This work demonstrates that the synthesis of 1 is viable and provides a springboard for the synthesis of low-coordinate complexes featuring this unusual bulky ligand.

Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	Chemistry
Publisher:	American Chemical Society
ISSN:	0020-1669
Funders:	EPSRC and Leverhulme Trust
Date of First Compliant Deposit:	17 October 2024
Date of Acceptance:	1 October 2024
Last Modified:	14 Nov 2024 14:21
URI:	https://orca.cardiff.ac.uk/id/eprint/173067

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