Dicyanomethylene-Functionalized S-Indacene-Based D-π-A-π-D Dyes Exhibiting Large Near-Infrared Two-Photon Absorption Cross-Section
Dyes and Pigments 2022
Arnis Žagata, Kaspars Traskovskis, Sergejs Beļakovs, Igors Mihailovs, Arturs Bundulis, Mārtiņš Rutkis

A series of centrosymmetric chromophores with D-π-A-π-D molecular architecture has been synthesized and characterized with respect to their third-order nonlinear optical (NLO) properties. The investigated compounds feature novel central electron acceptor fragments composed of derivatives of s-indacene-1,3,5,7(2H,6H)-tetraone (Janus dione), in which the carbonyls have been substituted by either two or four dicyanomethylene groups. Due to the increased electron acceptor strength, up to twofold increase in two-photon absorption (2 PA) cross-section is observed for the dyes in comparison to the structural analogues based on the parent compound. The best performing dye exhibits intensive 2 PA absorption band in 1000–1300 nm range with a peak cross-section value of 11,000 GM. Optical limiting was successfully demonstrated using the compound, marking the presented chemical design as a promising direction for optical power-limiting applications in the important near-infrared (NIR) spectral region.


DOI
10.1016/j.dyepig.2022.110864
Hipersaite
https://www.sciencedirect.com/science/article/pii/S0143720822007860?via%3Dihub

Žagata, A., Traskovskis, K., Beļakovs, S., Mihailovs, I., Bundulis, A., Rutkis, M. Dicyanomethylene-Functionalized S-Indacene-Based D-π-A-π-D Dyes Exhibiting Large Near-Infrared Two-Photon Absorption Cross-Section. Dyes and Pigments, 2022, Vol. 208, Article number 110864. ISSN 0143-7208. Pieejams: doi:10.1016/j.dyepig.2022.110864

Publikācijas valoda
English (en)
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