3 research outputs found

    One-Pot Synthesis of Mo<sup>0</sup> Dinitrogen Complexes Possessing Monodentate and Multidentate Phosphine Ligands

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    Mo<sup>0</sup> dinitrogen complexes bearing electron-rich mono- and bidentate phosphines can be synthesized in good yields from inexpensive and readily accessible MoCl<sub>5</sub> via a one-step mild reduction with Mg metal. <i>trans</i>-[(N<sub>2</sub>)<sub>2</sub>Mo­(PMePh<sub>2</sub>)­(PPh­(CH<sub>2</sub>CH<sub>2</sub>PPh<sub>2</sub>)<sub>2</sub>)] can also be obtained via this strategy. However, in the presence of tri- and tetradentate ligands that are sterically restrictive, the analogous reduction leads to either (η<sup>6</sup>-arene) formation or [Mo­(multidentate phosphine)<sub><i>m</i></sub>]<sub><i>n</i></sub> oligomer complexes that have no dinitrogen ligands. One such η<sup>6</sup>-arene complex, where the Mo<sup>0</sup> center is ligated by 1,1,1-tris­(diphenylphosphinomethyl)­ethane, was isolated and characterized via X-ray crystallography

    One-Pot Synthesis of Mo<sup>0</sup> Dinitrogen Complexes Possessing Monodentate and Multidentate Phosphine Ligands

    No full text
    Mo<sup>0</sup> dinitrogen complexes bearing electron-rich mono- and bidentate phosphines can be synthesized in good yields from inexpensive and readily accessible MoCl<sub>5</sub> via a one-step mild reduction with Mg metal. <i>trans</i>-[(N<sub>2</sub>)<sub>2</sub>Mo­(PMePh<sub>2</sub>)­(PPh­(CH<sub>2</sub>CH<sub>2</sub>PPh<sub>2</sub>)<sub>2</sub>)] can also be obtained via this strategy. However, in the presence of tri- and tetradentate ligands that are sterically restrictive, the analogous reduction leads to either (η<sup>6</sup>-arene) formation or [Mo­(multidentate phosphine)<sub><i>m</i></sub>]<sub><i>n</i></sub> oligomer complexes that have no dinitrogen ligands. One such η<sup>6</sup>-arene complex, where the Mo<sup>0</sup> center is ligated by 1,1,1-tris­(diphenylphosphinomethyl)­ethane, was isolated and characterized via X-ray crystallography

    Efficient Carbene and Carbyne Formation in Molybdenum(0) and Tungsten(0) Dinitrogen Complexes

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    Zerovalent group 6 dinitrogen phosphine complexes react with 3,3-diphenylcyclopropene to give vinylcarbyne hydride complexes that have been characterized crystallographically. Computational studies indicate that the observed products resulted from the α-migration and rearrangement of an initially formed vinylcarbene
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