2 research outputs found
Generation of Powerful Tungsten Reductants by Visible Light Excitation
The
homoleptic arylisocyanide tungsten complexes, WÂ(CNXy)<sub>6</sub> and
WÂ(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 WÂ(CNXy)<sub>6</sub> and WÂ(CNIph)<sub>6</sub> with
lifetimes of 17 and 73 ns, respectively. Diffusion-controlled energy
transfer from electronically excited WÂ(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]Â[PF<sub>6</sub>], to the THF solution promotes formation of electron transfer
(ET) quenching products, [WÂ(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]Â[PF<sub>6</sub>]/THF solutions. The estimated reduction potential for the
[WÂ(CNIph)<sub>6</sub>]<sup>+</sup>/*W couple is −2.8 V vs Cp<sub>2</sub>Fe<sup>+/0</sup>, establishing WÂ(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
The
homoleptic arylisocyanide tungsten complexes, WÂ(CNXy)<sub>6</sub> and
WÂ(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 WÂ(CNXy)<sub>6</sub> and WÂ(CNIph)<sub>6</sub> with
lifetimes of 17 and 73 ns, respectively. Diffusion-controlled energy
transfer from electronically excited WÂ(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]Â[PF<sub>6</sub>], to the THF solution promotes formation of electron transfer
(ET) quenching products, [WÂ(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]Â[PF<sub>6</sub>]/THF solutions. The estimated reduction potential for the
[WÂ(CNIph)<sub>6</sub>]<sup>+</sup>/*W couple is −2.8 V vs Cp<sub>2</sub>Fe<sup>+/0</sup>, establishing WÂ(CNIph)<sub>6</sub> as one
of the most powerful photoreductants that has been generated with
visible light