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Elucidation of the aqueous equilibrium system of IrH₂(PMe₃)₃Cl and periodic trends of the iridium (III) dihydrido tris(trimethylphosphino) series, IrH₂(PMe₃)₃X

Abstract

dc:description.abstract

The complex, IrH₂(PMe₃)₃Cl (1), was previously found to be, not only unexpectedly water-soluble but also an effective homogeneous catatyst for the hydrogenation of unsaturates in water. The results of extensive ³¹P NMR studies on the aqueous system of (1) indicate that (1) is in equilibrium with the iridium(III) dihydrido “aquo” complex, [IrH₂(PMe₃)₃(H₂O)]⁺, and not the μ-chloro bridged complex, { [IrH₂(PMe₃)₃]₂Cl}⁺ (2), as previously reported. The calculated K<sub>eq</sub> value for the aqueous equilibrium is (0.0037 ± 0.0003) M. Thermodynamic data (ΔH = 30.8 kJ/mol, ΔS = 56.0 J/(Kmol), and ΔG = 14.1 kJ/mol) obtained from variable temperature ³¹P NMR studies are consistent with the proposed equilibrium system. The complexes IrH₂(PMe₃)₃X (X = O₂CPh (3), I (4), and Br (6) were synthesized and examined. The complexes IrH₂(PMe₃)₃X (X = H₂O and F) could not be isolated. (3) was determined to dissociate completely in water to form the iridium(III) dihydrido “‘aquo” complex, [IrH₂(PMe₃)₃(H₂O)]⁺, seemingly explaining the greater catalytic activity of (3). Solubility of the halo complexes decreased from moderately soluble (1), to slightly soluble (6), to very slightly soluble (4). The solubilities of (4) and (6) were too low to allow quantification of their equilibria. Finally it was observed that linear relationships exist between the electronegativity of the ligand, X, and the ¹H and ³¹P NMR chemical shifts of the hydrides and the phosphines for the complexes, IrH₂(PMe₃)₃X. These relationships are consistent with the findings of Birnbaum.

Degree

thesis:*
Name thesis:degree_name
Ph. D.
Level thesis:degree_level
doctoral
Discipline thesis:degree_discipline
Chemistry
Department dc:contributor.department
Chemistry
Grantor dc:publisher
Virginia Tech
Year dc:date.issued
1994

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Matthews, Kelly E.
Chair dc:contributor.committeechair
  • Merola, Joseph S.
Committee members dc:contributor.committeemember
  • Brewer, Karen J.
  • Dillard, John G.
  • Glanville, James O.
  • Hanson, Brian E.

Rights

dc:rights
Statement dc:rights
  • In Copyright
Language dc:language.iso
en

Identifiers

dc:identifier.*
Dc Identifier Other
etd-06062008-164037
OAI identifier oai:identifier
oai:vtechworks.lib.vt.edu:10919/38258

Chain of custody

source
Harvested from
Virginia Tech
Base URL
vtechworks.lib.vt.edu/oai/request
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
related terms
citation

Matthews, Kelly E.. Elucidation of the aqueous equilibrium system of IrH₂(PMe₃)₃Cl and periodic trends of the iridium (III) dihydrido tris(trimethylphosphino) series, IrH₂(PMe₃)₃X. doctoral thesis, Virginia Tech, 1994. http://hdl.handle.net/10919/38258