Synthesis and characterization of two-photon chromophores based on a tetrasubstituted tetraethynylethylene scaffold.

A new series of model dye molecules composed of three multibranched analogues based on the tetrasubstituted tetraethynylethylene structural motif have been synthesized and experimentally shown to possess strong and widely dispersed two-photon absorption (2PA) in the near-IR region. It was found that the spectral position of the major 2PA band could be tuned by the electronic nature of the selected substitution units. The studied model fluorophores also exhibited fairly low photodegradation of their fluorescence intensity even under prolonged UV-light irradiation, which is beneficial for the development of fluorescence probes that are needed for long-term light exposure.

Degenerate two-photon absorption and effective optical-power-limiting properties of multipolar chromophores derived from 2,3,8-trisubstituted indenoquinoxaline.

Two analogous multipolar chromophores (1 and 2) that contained 2,3,8-trisubstituted indenoquinoxaline moieties have been synthesized and characterized for their two-photon absorption properties, both in the femtosecond and nanosecond time regimes. We demonstrated that their multi-branched framework structures, which incorporated appropriately functionalized indenoquinoxaline units, afforded large molecular nonlinear absorptivities within the studied spectroscopic range. Effective optical-power-limiting and stabilization behaviors in the nanosecond regime of dye molecule (2) were also investigated and the results indicated that such a structural motif could be a useful approach to the molecular design of highly active two-photon systems for quick-response and related broadband optical-suppressing applications, in particular for confronting laser pulses of a long duration.