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[摘要]：The linear and non-linear optical properties of a family of dumbbell-shaped dinuclear complexes, in which an oligothiophene chain with various numbers of rings (1, 3, and 6) acts as a bridge between two homoleptic tris(2,2'-bipyridine)ruthenium(II) complexes, have been fully investigated by using a range of spectroscopic techniques (absorption and luminescence, transient absorption, Raman, and non-linear absorption), together with density functional theory calculations. Our results shed light on the impact of the synergistic collaboration between the electronic structures of the two chemical moieties on the optical properties of these materials. Experiments on the linear optical properties of these compounds indicated that the length of the oligothiophene bridge was critical for luminescent behavior. Indeed, no emission was detected for compounds with long oligothiophene bridges (compounds 3 and 4, with 3 and 6 thiophene rings, respectively), owing to the presence of the 3p?p* state of the conjugated bridge below the 3MLCT-emitting states of the end-capping RuII complexes. In contrast, the compound with the shortest bridge (2, one thiophene ring) shows excellent photophysical features. Non-linear optical experiments showed that the investigated compounds were strong non-linear absorbers in wide energy ranges. Indeed, their non-linear absorption was augmented upon increasing the length of the oligothiophene bridge. In particular, the compound with the longest oligothiophene bridge not only showed strong two-photon absorption (TPA) but also noteworthy three-photon-absorption behavior, with a cross-section value of 4X10-78 cm6?s2 at 1450 nm. This characteristic was complemented by the strong excited-state absorption (ESA) that was observed for compounds 3 and 4. As a matter of fact, the overlap between the non-linear absorption and ESA establishes compounds 3 and 4 as good candidates for optical-power-limiting applications. |
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