International audienceThe 2,7-fluorenyl-bridged Fe(?5-C5Me5)(?2-dppe)[C≡C(2,7-C13H6Bu2)C≡C]Fe(?5-C5Me5)(?2-dppe) (1a), its extended analogue Fe(?5-C5Me5)(?2-dppe)[C≡C(1,4-C6H4)C≡C(2,7-C13H6Bu2)C≡C(1,4-C6H4)C≡C](?5-C5Me5)(?2-dppe)Fe (1b), and the corresponding mononuclear complexes Fe(?5-C5Me5)(?2-dppe)[C≡C(2-C13H7Bu2)] (2a) and Fe(?5-C5Me5)(?2-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 performanc
A series of three conjugated meso-porphyrin dendrimers containing conjugated dendrons featuring 2,7-fluorenyl groups, incorporating overall 8, 12, or 28 fluorenyl units have been synthesized and characterized. The photophysical properties of these new compounds were studied in the context of photodynamic therapy. The relevant linear and nonlinear optical properties were measured in organic media and useful structure-properties relationships were derived.
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