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    Fe<sup>II</sup> Hexa <i>N</i>‑Heterocyclic Carbene Complex with a 528 ps Metal-to-Ligand Charge-Transfer Excited-State Lifetime

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    The iron carbene complex [Fe<sup>II</sup>(btz)<sub>3</sub>]­(PF<sub>6</sub>)<sub>2</sub> (where btz = 3,3′-dimethyl-1,1′-bis­(<i>p</i>-tolyl)-4,4′-bis­(1,2,3-triazol-5-ylidene)) has been synthesized, isolated, and characterized as a low-spin ferrous complex. It exhibits strong metal-to-ligand charge transfer (MLCT) absorption bands throughout the visible spectrum, and excitation of these bands gives rise to a <sup>3</sup>MLCT state with a 528 ps excited-state lifetime in CH<sub>3</sub>CN solution that is more than one order of magnitude longer compared with the MLCT lifetime of any previously reported Fe<sup>II</sup> complex. The low potential of the [Fe­(btz)<sub>3</sub>]<sup>3+</sup>/[Fe­(btz)<sub>3</sub>]<sup>2+</sup> redox couple makes the <sup>3</sup>MLCT state of [Fe<sup>II</sup>(btz)<sub>3</sub>]<sup>2+</sup> a potent photoreductant that can be generated by light absorption throughout the visible spectrum. Taken together with our recent results on the [Fe<sup>III</sup>(btz)<sub>3</sub>]<sup>3+</sup> form of this complex, these results show that the Fe<sup>II</sup> and Fe<sup>III</sup> oxidation states of the same Fe­(btz)<sub>3</sub> complex feature long-lived MLCT and LMCT states, respectively, demonstrating the versatility of iron <i>N-</i>heterocyclic carbene complexes as promising light-harvesters for a broad range of oxidizing and reducing conditions
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