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An Intramolecular NH⋅⋅⋅(-H)Re2 Dihydrogen Bond and a Novel 3-2 Coordination Mode of the Pyrazolate Anion on a Triangular Cluster Face
- Source :
- Chemistry - A European Journal. 8:5340-5350
- Publication Year :
- 2002
- Publisher :
- Wiley, 2002.
-
Abstract
- The quantitative addition of pyrazole (Hpz) to the 44 valence-electron, triangular cluster anion [Re3(μ3-H)(μ-H)3(CO)9]− gives the novel unsaturated anion [Re3(μ-H)4(CO)9(Hpz)]− (1, 46 valence electrons), which contains a pyrazole molecule that is terminally coordinated on a cluster vertex. Solid-state X-ray and IR analyses reveal a rather weak hydrogen-bonding interaction between the NH proton and one of the hydrides bridging the opposite triangular cluster edge (ΔH°=−3.1 kcal mol−1 from the Iogansen equation). Both IR and NMR data indicate that such a proton–hydride interaction is maintained in the major conformer present in CD2Cl2, but also provide evidence of the presence of minor conformers of 1 in which the NH proton is involved in an intermolecular hydrogen bond with the solvent. The μ-H⋅⋅⋅HN bond length evaluated in solution through the T1 minimum value (2.07 A) and that determined in the solid state by X-ray diffraction (2.05 A) are in good agreement. NMR experiments show that, in acetone, intermolecular NH⋅⋅⋅solvent interactions replace the intramolecular dihydrogen bond. At room temperature in CH2Cl2, the pyrazole ligand in 1 is labile and 1 slowly “disproportionates” to [Re3(μ3-H)(μ-H)3(CO)9]− and [Re3(μ-H)3(CO)9(μ-η2-pz)(Hpz)]−, with H2 evolution. Slow H2 evolution also leads to the formation of the anion [Re3(μ-H)3(CO)9(pz)]− (5), in which the pyrazolate anion adopts a novel μ3-η2-coordination mode, as revealed by a single-crystal X-ray analysis. The analysis of the bond lengths indicates that the pyrazolate anion in 5 acts as a six-electron donor, with loss of the aromaticity. The formation of 5 from 1 is much faster in solvents with a high dielectric constant, such as acetone or DMF. Anion 5 was also obtained from the reaction of pyrazole with [Re3(μ-H)3(CO)9(μ3-CH3)]− through the intermediate formation of two isomeric addition derivatives and following CH4 evolution.
Details
- ISSN :
- 15213765 and 09476539
- Volume :
- 8
- Database :
- OpenAIRE
- Journal :
- Chemistry - A European Journal
- Accession number :
- edsair.doi...........e9f63cd92572302a5a60018330dd4aa8
- Full Text :
- https://doi.org/10.1002/1521-3765(20021202)8:23<5340::aid-chem5340>3.0.co;2-s