Structure and dynamics in metal phosphine complexes using advanced NMR studies with para-hydrogen induced polarisation

Barbara A. Messerle*, Christopher J. Sleigh, Martin G. Partridge, Simon B. Duckett

*Corresponding author for this work

Research output: Contribution to journalArticle

52 Citations (Scopus)

Abstract

The iridium and rhodium phosphine complexes IrCl(CO)(PPh3)2 1 (Vaska's complex), Rh(PMe3)4Cl 2, and Rh(PMe3)3Cl 3, add H2 to form the corresponding dihydrides. Exchange with para-hydrogen (p-H2) provides a means of observing 1H NMR signals due to the metal bound hydrides at significantly enhanced levels of sensitivity. We show that monitoring these metal hydride complexes can be achieved by a range of 2D NMR methods, based on standard experiments, which have been modified to achieve optimum signal. The assignment of heteronuclei, including low sensitivity nuclei such as 103Rh, determination of heteronuclear coupling constants and measurement of their relative signs, is described for these systems using p-H2 derived starting magnetisation. In the case of Vaska's complex the dihydride addition product contains a trans labilised carbonyl ligand, and substitution with appropriate phosphines brings about the formation of metal phosphine complexes with new ligand spheres. Appropriately modified NOESY experiments are demonstrated to rapidly probe structural arrangements, and monitor dihydride exchange. For Ir(H)2Cl(PPh3)3 dihydride exchange is shown to proceed mainly via Ir(H)2Cl(PPh3)2, which is shown to contain inequivalent hydrides. The reactivity of the arsine complex IrCl(AsPh3)3 9 towards H2 is examined, and the NOESY approach used to make structural assignments in the reaction product.

Original languageEnglish
Pages (from-to)1429-1435
Number of pages7
JournalJournal of the Chemical Society. Dalton Transactions
Issue number9
Publication statusPublished - 7 May 1999
Externally publishedYes

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