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2,7-Fluorenediyl-Bridged Complexes Containing Electroactive “Fe(η5‑C5Me5)(κ2‑dppe)CC–” End Groups: Molecular Wires and Remarkable Nonlinear Electrochromes

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Figshare2016-02-12 更新2026-04-29 收录
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https://figshare.com/articles/dataset/2_7_Fluorenediyl_Bridged_Complexes_Containing_Electroactive_Fe_sup_5_sup_C_sub_5_sub_Me_sub_5_sub_sup_2_sup_dppe_C_C_End_Groups_Molecular_Wires_and_Remarkable_Nonlinear_Electrochromes/2106463
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The 2,7-fluorenyl-bridged Fe­(η5-C5Me5)­(κ2-dppe)­[CC­(2,7-C13H6Bu2)­CC]­Fe­(η5-C5Me5)­(κ2-dppe) (1a), its extended analogue Fe­(η5-C5Me5)­(κ2-dppe)­[CC­(1,4-C6H4)­CC­(2,7-C13H6Bu2)­CC­(1,4-C6H4)­CC]­(η5-C5Me5)­(κ2-dppe)Fe (1b), and the corresponding mononuclear complexes Fe­(η5-C5Me5)­(κ2-dppe)­[CC­(2-C13H7Bu2)] (2a) and Fe­(η5-C5Me5)­(κ2-dppe)­[CC­(1,4-C6H4)­CC­(2-C13H7Bu2)] (2b), which model half of these molecules, have been synthesized and characterized in their various redox states. The molecular wire characteristics of the dinuclear complexes were examined in their mixed-valent states, with progression from 1a[PF6] to 1b[PF6] resulting in a sharp decrease in electronic coupling. The cubic nonlinear optical properties of these species were investigated over the visible and near-IR range, a particular emphasis being placed on their multiphoton absorption properties; the complexes are shown to function as redox-switchable nonlinear chromophores at selected wavelengths, and the more extended derivatives are shown to exhibit the more promising NLO performance.
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2016-02-12
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