2 research outputs found

    Generation of Powerful Tungsten Reductants by Visible Light Excitation

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    The homoleptic arylisocyanide tungsten complexes, W­(CNXy)<sub>6</sub> and W­(CNIph)<sub>6</sub> (Xy = 2,6-dimethylphenyl, Iph = 2,6-diisopropylphenyl), display intense metal to ligand charge transfer (MLCT) absorptions in the visible region (400–550 nm). MLCT emission (λ<sub>max</sub> ≈ 580 nm) in tetrahydrofuran (THF) solution at rt is observed for W­(CNXy)<sub>6</sub> and W­(CNIph)<sub>6</sub> with lifetimes of 17 and 73 ns, respectively. Diffusion-controlled energy transfer from electronically excited W­(CNIph)<sub>6</sub> (*W) to the lowest energy triplet excited state of anthracene (anth) is the dominant quenching pathway in THF solution. Introduction of tetrabutylammonium hexafluorophosphate, [Bu<sup><i>n</i></sup><sub>4</sub>N]­[PF<sub>6</sub>], to the THF solution promotes formation of electron transfer (ET) quenching products, [W­(CNIph)<sub>6</sub>]<sup>+</sup> and [anth]<sup>•–</sup>. ET from *W to benzophenone and cobalticenium also is observed in [Bu<sup><i>n</i></sup><sub>4</sub>N]­[PF<sub>6</sub>]/THF solutions. The estimated reduction potential for the [W­(CNIph)<sub>6</sub>]<sup>+</sup>/*W couple is −2.8 V vs Cp<sub>2</sub>Fe<sup>+/0</sup>, establishing W­(CNIph)<sub>6</sub> as one of the most powerful photoreductants that has been generated with visible light

    Generation of Powerful Tungsten Reductants by Visible Light Excitation

    No full text
    The homoleptic arylisocyanide tungsten complexes, W­(CNXy)<sub>6</sub> and W­(CNIph)<sub>6</sub> (Xy = 2,6-dimethylphenyl, Iph = 2,6-diisopropylphenyl), display intense metal to ligand charge transfer (MLCT) absorptions in the visible region (400–550 nm). MLCT emission (λ<sub>max</sub> ≈ 580 nm) in tetrahydrofuran (THF) solution at rt is observed for W­(CNXy)<sub>6</sub> and W­(CNIph)<sub>6</sub> with lifetimes of 17 and 73 ns, respectively. Diffusion-controlled energy transfer from electronically excited W­(CNIph)<sub>6</sub> (*W) to the lowest energy triplet excited state of anthracene (anth) is the dominant quenching pathway in THF solution. Introduction of tetrabutylammonium hexafluorophosphate, [Bu<sup><i>n</i></sup><sub>4</sub>N]­[PF<sub>6</sub>], to the THF solution promotes formation of electron transfer (ET) quenching products, [W­(CNIph)<sub>6</sub>]<sup>+</sup> and [anth]<sup>•–</sup>. ET from *W to benzophenone and cobalticenium also is observed in [Bu<sup><i>n</i></sup><sub>4</sub>N]­[PF<sub>6</sub>]/THF solutions. The estimated reduction potential for the [W­(CNIph)<sub>6</sub>]<sup>+</sup>/*W couple is −2.8 V vs Cp<sub>2</sub>Fe<sup>+/0</sup>, establishing W­(CNIph)<sub>6</sub> as one of the most powerful photoreductants that has been generated with visible light
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