Nonlinear optical spectroscopy of new squaraine derivatives with high potential for multidisciplinary applications

New symmetrical anilinosquaraine derivatives with four hydroxyl groups in the molecular core, namely, 2,4-bis[4-[4-(3,5-didecoxyphenoxy)butyl-methyl-amino]-2,6-dihydroxy-phenyl]squaraine (1) and 2,4-bis[4-[6-(3,5-didecoxyphenoxy)hexyl-methyl-amino]-2,6-dihydroxy-phenyl]squaraine (2), were synthesized. Both compounds were found to exhibit manifold linear spectroscopic and nonlinear optical properties with high potential for a number of important multidisciplinary applications. Linear photophysical and photochemical properties of 1 and 2 were assessed in liquid solvents of different polarities at room temperature, including steady-state absorption, emission, and excitation anisotropy spectra, along with fluorescence quantum yields and lifetimes. The fast intramolecular relaxation processes in 1 and 2 were analyzed using femtosecond transient absorption pump-probe spectroscopy, and unusually strong optical amplification (gain) was observed in their narrow fluorescence contours without any evidence of solvent reorganization phenomena. The degenerate two-photon absorption (2PA) spectra of 1 and 2 were measured in a broad spectral range, and a maximum 2PA cross-section of ≈2000 GM was observed. The effect of the superluminescence of 1 and 2 was observed under femtosecond pumping, which extended their potential for photonic applications.

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Publication Details

Journal
Physical Chemistry Chemical Physics
Published
2025-01-01
DOI
https://doi.org/10.1039/d5cp00144g
Citations
1
Primary Topic
Porphyrin and Phthalocyanine Chemistry
Type
article
Field-Weighted Citation Impact
0.52

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article

Nonlinear optical spectroscopy of new squaraine derivatives with high potential for multidisciplinary applications

Iaroslav B. Kuziv, Yu. P. Piryatinskiĭ, Mykhailo V. Bondar, Andriy Dmytruk et al.
1 citations
Physical Chemistry Chemical Physics
Porphyrin and Phthalocyanine Chemistry
0.52
article

Nonlinear optical spectroscopy of new squaraine derivatives with high potential for multidisciplinary applications

Iaroslav B. Kuziv, Yu. P. Piryatinskiĭ, Mykhailo V. Bondar, Andriy Dmytruk, A. O. Kostetskyi, I. Ya. Dubey, N. V. Bashmakova, Ivan Blonskyi, Viktor Kadan, George V. Klishevich, Volodymyr O. Hryn
article en
1 citations

Abstract

New symmetrical anilinosquaraine derivatives with four hydroxyl groups in the molecular core, namely, 2,4-bis[4-[4-(3,5-didecoxyphenoxy)butyl-methyl-amino]-2,6-dihydroxy-phenyl]squaraine (1) and 2,4-bis[4-[6-(3,5-didecoxyphenoxy)hexyl-methyl-amino]-2,6-dihydroxy-phenyl]squaraine (2), were synthesized. Both compounds were found to exhibit manifold linear spectroscopic and nonlinear optical properties with high potential for a number of important multidisciplinary applications. Linear photophysical and photochemical properties of 1 and 2 were assessed in liquid solvents of different polarities at room temperature, including steady-state absorption, emission, and excitation anisotropy spectra, along with fluorescence quantum yields and lifetimes. The fast intramolecular relaxation processes in 1 and 2 were analyzed using femtosecond transient absorption pump-probe spectroscopy, and unusually strong optical amplification (gain) was observed in their narrow fluorescence contours without any evidence of solvent reorganization phenomena. The degenerate two-photon absorption (2PA) spectra of 1 and 2 were measured in a broad spectral range, and a maximum 2PA cross-section of ≈2000 GM was observed. The effect of the superluminescence of 1 and 2 was observed under femtosecond pumping, which extended their potential for photonic applications.

Physical Chemistry Chemical PhysicsVol. 27(26)
Taras Shevchenko National University of Kyiv (UA), Institute of Molecular Biology and Genetics (UA), Institute of Physics (UA)
Simons Foundation, National Research Foundation of Ukraine
Life below water
Openalex Percentile: Top 37%
Porphyrin and Phthalocyanine Chemistry
0.52
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