Complexes of the Platinum Metals. Part 32. Synthesis and Chemistry of some Iridium Sulphonate Derivatives

DOI: 10.1039/DT9870000947

Source and publish data:

Journal of the Chemical Society, Dalton Transactions p. 947 - 952 (1987)

Update date:2022-08-04

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Authors:

Harding, Alexander P.

Robinson, Stephen D.

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Article abstract of DOI:10.1039/DT9870000947

Sulphonic acids RSO3H (R = CF3, CH3, or C6H4CH3-p) react with mer-, , and to afford the products , , and respectively.Under more vigorous conditions the last reaction yields the bis(sulphonate) complexes .Thelability of the monodentate sulphonate ligands has been demonstrated by the substitution reactions of with a variety of neutral donor ligands.Products readily obtained in this manner include , 2 = 2,2'-bipyridyl, 1,10-phenanthroline, ethylenediamine, or o-NH2-C6H4NH2>, and trans-.Carbonylation of affords the tricarbonyl salt whereas under similar conditions the precursors (R = CH3 or C6H4CH3-p) yield the dihydride salts .Many of the complexes isolated were solvated by H-bonded molecules of sulphonic acids.Stereochemical assignments based on ¹H, ¹⁹F, and ³¹ n.m.r. data are given for all the new products reported.

Full text of DOI:10.1039/DT9870000947

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