Hexaruthenium Carbonyl Cluster Complexes with Basal Edge-Bridged Square Pyramidal Metallic Skeleton: Efficient Synthesis of 2-Imidopyridine Derivatives and Determination of Their Reactive Sites in Carbonyl Substitution Reactions
The reactions of [Ru3(CO)12] with half equivalent of 2-amino-6-methylpyridine (H2ampy) or 2-aminopyridine (H2apy) in refluxing xylene give the hexanuclear products [Ru6(μ3-H)2(μ5-η2-L)(μ-CO)2(CO)14] (L = ampy, 1; apy, 2). These reactions represent the first high-yield syntheses of hexanuclear comple...
Saved in:
Published in | Inorganic chemistry Vol. 43; no. 17; pp. 5450 - 5458 |
---|---|
Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Chemical Society
23.08.2004
|
Online Access | Get full text |
Cover
Loading…
Summary: | The reactions of [Ru3(CO)12] with half equivalent of 2-amino-6-methylpyridine (H2ampy) or 2-aminopyridine (H2apy) in refluxing xylene give the hexanuclear products [Ru6(μ3-H)2(μ5-η2-L)(μ-CO)2(CO)14] (L = ampy, 1; apy, 2). These reactions represent the first high-yield syntheses of hexanuclear complexes with a basal edge-bridged square pyramidal metallic skeleton. Five metal atoms of these complexes are bridged by the N-donor ligand in such a way that the edge-bridging metal atom is attached to the pyridine nitrogen, while the basal atoms of the square pyramid are capped by an imido fragment that arises from the activation of both N−H bonds of the NH2 group. The reactive sites of these complexes in CO substitution reactions have been determined by studying the reactivity of 1 with triphenylphosphine. Two kinetically controlled monosubstitutions take place on the edge-bridging metal atom in positions cis to the pyridine nitrogen, leading to a mixture of two isomers of formula [Ru6(μ3-H)2(μ5-η2-ampy)(μ-CO)2(CO)13(PPh3)] (3 and 4). On heating at 80 °C, these monosubstituted isomers are transformed, via a dissociative pathway, into the product of thermodynamic control (5), which has the PPh3 ligand on the apical Ru atom. The di- and trisubstituted derivatives [Ru6(μ3-H)2(μ5-η2-ampy)(μ-CO)2(CO)12(PPh3)2] (6) and [Ru6(μ3-H)2(μ5-η2-ampy)(μ-CO)2(CO)11(PPh3)3] (7) are stepwise formed from 3−5 and PPh3. Compound 6 has the PPh3 ligands on the edge-bridging and apical Ru atoms, and compound 7 has an additional PPh3 ligand on an unbridged basal Ru atom. The compound [Ru6(μ3-H)2(μ5-η2-ampy)(μ-CO)2(CO)12(μ-dppm)] (8), in which a basal and the apical Ru atoms are spanned by the dppm ligand, has been isolated from the reaction of 1 with bis(diphenylphosphino)methane. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0020-1669 1520-510X |
DOI: | 10.1021/ic0492789 |