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Comparative Bonding Behavior of Functional Cyclopentadienyl Ligands and Boron-Containing Analogues in Heterometallic Complexes and Clusters

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posted on 24.07.2006, 00:00 by Pierre Croizat, Nicolas Auvray, Pierre Braunstein, Richard Welter
The reactivity of isolobal molybdenum carbonylmetalates containing a 2-boratanaphthalene, [Mo(η5-2,4-MeC9H6BMe)(CO)3]- (5a) and [Mo(η5-2,4-MeC9H6BNi-Pr2)(CO)3]- (5b), a 1-boratabenzene, [Mo(η5-3,5-Me2C5H3BNi-Pr2)(CO)3]- (8), or a functionalized cyclopentadienyl ligand, the new metalate [Mo(η5-C5H4Ph)(CO)3]- (7) and [Mo(η5-C5H4NMe2)(CO)3]- (9), toward palladium (I and II) or platinum (I and II) complexes, such as trans-[PdCl2(NCPh)2], [Pd2(NCMe)6](BF4)2, trans-[PtCl2(PEt3)2], and [N(n-Bu)4]2 [Pt2Cl4(CO)2], has been investigated, and this has allowed an evaluation of the influence of the π-bonded ligands on the structures and unprecedented coordination modes observed in the resulting metal−metal-bonded heterometallic clusters. The new 58 CVE planar-triangulated centrosymmetric clusters, [Mo2Pd25-C5H4Ph)2(CO)6(PEt3)2] (11), [Mo2Pd25-2,4-MeC9H6BNi-Pr2)2(CO)6] (12), [Mo2Pd25-3,5-Me2C5H3BNi-Pr2)2(CO)6] (13), [Mo2Pd25-C5H4NMe2)2(CO)6(PEt3)2] (15), [Mo2Pt25-C5H4NMe2)2(CO)6(PEt3)2] (16), and [Mo2Pt25-C5H4NMe2)2(CO)8] (20), have been characterized by single-crystal X-ray diffraction. Their structural features were compared with those of the 54 CVE cluster [Re2Pd25-C4H4BPh)2(CO)6)] (4), previously obtained from the borole-containing metalate [Re(η5-C4H4BPh)(CO)3]- (2), in which a 2e−3c B−Cipso−Pd interaction involving the π-ring was observed. As an extension of what has been observed in 4, clusters 12 and 13 present a direct interaction of the boratanaphthalene (12) and the boratabenzene (13) ligands with palladium. In clusters 11, 15, 16, and 20, the π-ring does not interact with the palladium (11 and 15) or platinum centers (16 and 20), which confers to these clusters a geometry very similar to that of [Mo2Pd25-C5H5)2(CO)6(PEt3)2] (3b). The carbonylmetalates [Mo(π-ring)(CO)3]- are thus best viewed as formal four electron donors which bridge a dinuclear d9−d9 unit. The orientation of this building block in the clusters influences the shape of their metal cores and the bonding mode of the bridging carbonyl ligands. The crystal structure of new centrosymmetric complex [Mo(η5-C5H4Ph)(CO)3]2 (10) was determined, and it revealed intramolecular contacts of 2.773(4) Å between the carbon atoms of carbonyl groups across the metal−metal bond and intermolecular bifurcated interactions between the carbonyl oxygen atoms (2.938(4) and 3.029(4) Å), as well as intermolecular C−H···πAr(CC) interactions (2.334(3) and 2.786(4) Å) involving the phenyl substituents.