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Azole assisted C-H bond activation promoted by an osmium-polyhydride: Discerning between N and NH

AutorEguillor, Beatriz ; Esteruelas, Miguel A. ; Fernández, Israel; Gómez-Gallego, Mar; Lledós, Agustí; Martín-Ortíz, Mamen; Oliván, Montserrat ; Oñate, Enrique ; Sierra, Miguel A.
Fecha de publicación2015
EditorAmerican Chemical Society
CitaciónOrganometallics 34(10): 1898-1910 (2015)
ResumenThe capacity of the hexahydride complex OsH6(PiPr3)2 (1) to discern between the nitrogen atom and the NH unit in the azole assisted aryl C−H bond activation has been investigated. Complex 1 reacts with 2-phenylimidazole to give OsH3{κ2-C,N-(C6H4-imidazole)}(PiPr3)2 (2), which has been characterized by X-ray diffraction analysis. The structure proves the higher affinity of the metal center for the N atom in the presence of the NH unit, which remains unchanged, and reveals that in the solid state the molecules of this complex form infinite chains by means of intermolecular asymmetric 3-center bifurcated dihydrogen bonds. In solution, 1HDOSY NMR experiments suggest that the association degree decreases as the temperature increases. The fused six-membered ring of benzimidazole weakens the NH bond, enhancing its reactivity. As a consequence, complex 1 cannot discern between the N atom and the NH unit of 2-phenylbenzimidazole. Thus, the treatment of 1 with this substrate leads to a mixture of OsH3{κ2-C,N-(C6H4-benzimidazole)}(PiPr3)2 (3) and the dinuclear species (PiPr3)2H3Os(C6H4-benzimidazolate)OsH(η2-H2)(PiPr3)2 (4). The latter is the result of a N-assisted ortho-C−H bond activation of the phenyl group promoted by 0.5 equiv of 1 and the N−H bond activation promoted by the remaining 0.5 equiv of hexahydride 1 along with the agostic coordination of the remaining ortho-C−H bond to the metal center of the unsaturated fragment OsH(η 2-H2)(PiPr3)2. The comparison of the redox properties of 3 and 4 suggests that the interaction between the metal centers in the dinuclear compound is negligible. The replacement of the NH group of the azoles by a sulfur atom does not modify the behavior of the substrates. Thus, the reactions of 1 with 2-phenylthiazole and 2-phenylbenzothiazole afford OsH3{κ 2-C,N-(C6H4-thiazole)}(PiPr3)2 (5) and OsH3{κ2-C,N-(C6H4-benzothiazole)}(PiPr3)2 (6). In turn, complexes 2, 3, 5, and 6 are phosphorescent.
DescripciónThis is an open access article published under a Creative Commons Attribution (CC-BY) License.
Versión del editorhttp://dx.doi.org/10.1021/acs.organomet.5b00174
URIhttp://hdl.handle.net/10261/118255
DOI10.1021/acs.organomet.5b00174
Identificadoresdoi: 10.1021/acs.organomet.5b00174
issn: 0276-7333
e-issn: 1520-6041
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