Heterometallic complexes and clusters with 2-boratanaphthalene ligands
Identifieur interne : 000035 ( France/Analysis ); précédent : 000034; suivant : 000036Heterometallic complexes and clusters with 2-boratanaphthalene ligands
Auteurs : Pierre Braunstein [France] ; Elisabeth Cura [France] ; Gerhard E. Herberich [Allemagne]Source :
- Journal of the Chemical Society, Dalton Transactions [ 1472-7773 ] ; 2001.
English descriptors
- Teeft :
- Bond distances, Bond lengths, Braunstein, Carbonyl ligands, Chem, Crystal structure, Crystal structures, Crystallographic details, Dalton trans, Diastereomeric mixture, Donor metalloligand, Double bond character, Herberich, Irel, Isolobal, Isolobal analogy, Ligand, Mass spectrometry, Mmol, Molecular structure, Nipr2, Ortep view, Pentane, Single crystals, Solid hgcl2, Soluble, Stable powder, Toluene, Toluene solution, Trans, Valence electron.
Abstract
The new lithium (2-boratanaphthalene)tricarbonylmolybdates Li[Mo(RBn)(CO)3] (Bn = η5-C10H9B; R = NiPr2, Me) have been prepared and used as nucleophilic reagents for the synthesis of metal–metal bonded complexes and clusters. Dinuclear [(iPr2NBn)(OC)3Mo–Au(PPh3)] (7) and trinuclear [Hg{Mo(CO)3(iPr2NBn)}2] (9) and [Ag{Mo(CO)3(iPr2NBn)}{Mo(CO)3[(iPr2HN)Bn]}] (13) chain complexes have been obtained in which the metalate behaves as an anionic two-electron donor metalloligand. In 13, the other metal carbonyl fragment consists of an N-protonated (2-boratanaphthalene)tricarbonylmolybdenum fragment and acts therefore as a neutral, two-electron donor. In the 58-cluster valence electron planar, triangulated cluster [Mo2Pd2(MeBn)2(CO)6(PEt3)2] (15), the [Mo(MeBn)(CO)3]− fragment is however best viewed as a four-electron donor metalloligand bridging the Pd–Pd bond. These bonding situations are compared with those observed in complexes prepared from the metalate [MoCp(CO)3]− (Cp = η5-C5H5) and this establishes experimentally the isoelectronic and isolobal character of the [Mo(MeBn)(CO)3]− and [MoCp(CO)3]− fragments. The crystal structures of complexes 7, 9, 13 and 15 have been determined by X-ray diffraction.
Url:
DOI: 10.1039/b101556g
Affiliations:
- Allemagne, France
- Alsace (région administrative), District de Cologne, Grand Est, Rhénanie-du-Nord-Westphalie
- Aix-la-Chapelle, Strasbourg
- Université Strasbourg 1
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<term>Crystal structure</term>
<term>Crystal structures</term>
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<front><div type="abstract">The new lithium (2-boratanaphthalene)tricarbonylmolybdates Li[Mo(RBn)(CO)3] (Bn = η5-C10H9B; R = NiPr2, Me) have been prepared and used as nucleophilic reagents for the synthesis of metal–metal bonded complexes and clusters. Dinuclear [(iPr2NBn)(OC)3Mo–Au(PPh3)] (7) and trinuclear [Hg{Mo(CO)3(iPr2NBn)}2] (9) and [Ag{Mo(CO)3(iPr2NBn)}{Mo(CO)3[(iPr2HN)Bn]}] (13) chain complexes have been obtained in which the metalate behaves as an anionic two-electron donor metalloligand. In 13, the other metal carbonyl fragment consists of an N-protonated (2-boratanaphthalene)tricarbonylmolybdenum fragment and acts therefore as a neutral, two-electron donor. In the 58-cluster valence electron planar, triangulated cluster [Mo2Pd2(MeBn)2(CO)6(PEt3)2] (15), the [Mo(MeBn)(CO)3]− fragment is however best viewed as a four-electron donor metalloligand bridging the Pd–Pd bond. These bonding situations are compared with those observed in complexes prepared from the metalate [MoCp(CO)3]− (Cp = η5-C5H5) and this establishes experimentally the isoelectronic and isolobal character of the [Mo(MeBn)(CO)3]− and [MoCp(CO)3]− fragments. The crystal structures of complexes 7, 9, 13 and 15 have been determined by X-ray diffraction.</div>
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